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Extracellular vesicles: how they interact with endothelium, potentially contributing to metastatic cancer cell implants
© The Author(s) 2017
Received: 12 July 2017
Accepted: 13 August 2017
Published: 21 September 2017
Extracellular vesicles (EV) are blebs of cellular membranes, which entrap small portions of subjacent cytosol. They are released from a variety of cells, circulate in the blood for an unknown length of time and come to rest on endothelial surfaces. They contribute to an array of physiologic pathways, the complexity of which is still being investigated. They contribute to metastatic malignant cell implants and tumor-related angiogenesis, possibly abetted by the tissue factor that they carry. It is thought that the adherence of the EV to endothelium is dependent upon a combination of their P-selectin glycoprotein ligand-1 and exposed phosphatidylserine, the latter of which is normally hidden on the inner bilayer of the intact cellular membrane. This manuscript reviews what is known about EV origins, their clearance from the circulation and how they contribute to malignant cell implants upon endothelium surfaces and subsequent tumor growth.
Definition of extracellular vesicles
Cells shed blebs of their phospholipid bilayer plasma membranes as byproducts of cell growth, apoptosis and in response to physiologic and pathophysiologic stimuli. These vesicles encapsulate small portions of the subjacent cytosol, creating a heterogeneous population of phospholipid-walled vesicles. These particles are referred to as extracellular vesicles (EV), but also as microparticles, microvesicles, microsomes, lipid vesicles, apoptotic blebs and exosomes [1–6].
EV’s are characterized by their size (30–100 nm for exosomes and 100–1000 nm diameter for the larger microvesicles), by their cells of origin including megakaryocytes, platelets, red blood cells, endothelial cells and others, and by their intravesicular contents [2, 3, 6, 7]. Their intravesicular contents depend upon their cells of origin and can include tissue factor, double stranded DNA, mRNA, microRNA, adhesion integrins, growth factors, protease inhibitors, P-selectin glycoprotein ligand-1 (PSGL-1) and ceramides [8–17]. They have been detected in blood plasma and other physiologic fluids [3, 4]. Gender, age of subjects and diseases influence their number in circulating blood and their size distribution [18, 19].
EVs are also released in response to pathophysiologic stimuli including thrombin, shear stress, complement activation, sepsis, hypoxia, inflammation, from malignant cells and following chemotherapy for malignancies [20–22]. They may also be byproducts of cell maturation with shedding of excess cell membrane .
Exosomes are unique subsets of EVs with specific biogenesis, measuring 30–100 nm [4, 17]. They are derived from endosomal multivesicular bodies, which then fuse with plasma membranes and are secreted from the cell into extracellular space, a process termed exocytosis. The primary function of these endosomes appears to be for the cellular uptake and extrusion of macromolecules from and to the extracellular fluids [1–3, 27]. They transport bioactive molecules including proteins, DNA, functional mRNA and microRNA from cell to cell by membranous transfer, thereby influencing other cell systems [17, 25, 28]. The currently available techniques do not allow for clean separation of these exosomes from the larger extracellular vesicles.
Apoptotic bodies may co-isolate with extracellular vesicles when isolated in the lab, but based upon origin they differ greatly from EV . The EV appear to be generated continuously from normal, viable cells, while the apoptotic bodies are derived following a highly regulated programmed cell death, in which the caspase pathway plays a central role. Apoptosis involves cell shrinkage and nuclear fragmentation, with the debris separated into nuclear or cytoplasmic vesicles of various sizes, which may be as small as the EV, but also may be up to 5000 nm diameter. They do express the “eat me” cellular signal to facilitate their phagocytosis by macrophages in the vicinity of the dead cell, using some of the same signals as the other EV .
Methods of isolation
The methods of isolation and preservation of the EVs are improving, but have not reached the ultimate goal of allowing analysis of homogeneous EV subpopulations and precise study of their targets [3–5, 30]. Currently EVs are defined predominantly by the techniques used for their isolation (flow cytometry, density gradient separation, differential centrifugation, size-exclusion chromatography, immunoaffinity isolation, polymer precipitation and others) as they affect the size and density of the isolates. Also, pre-analytical manipulation of samples influence the study results . As of now there is overlap of the size subclasses and cells of origin [4, 5]. For reporting purposes the EV can be further described by flow cytometry, mass spectroscopy and by their specific contents such as DNA, microRNA and mRNA [3, 32, 33].
A new technique for isolation of EV was reported using affinity-based methodology taking advantage of the T cell immunoglobulin domain and mucin-containing protein 4, known as Tim4, and its adherence to the externalized plasma membrane phosphatidylserine . In this method the extracellular domain of Tim4, normally expressed as a transmembrane protein on macrophages, is immobilized on magnetic beads. Since Tim4 strongly binds to phosphatidylserine it immobilizes the EV on the beads . This binding is calcium dependent and thus EV can be released when calcium chelators are added. Tim4 affinity can also be used in ELISA and flow cytometry formats .
Post-translational modifications of EV proteins are under study [3, 36, 37]. Exosomes become more rigid increasing their stability after they are released from m into the extracellular space with its increased pH. They also undergo post-translational covalent attachment to fatty acids. Acetylation and myristoylation promote protein sorting and subsequent EV budding [36, 38].
Total mass of EVs in circulation
The total mass of EVs in the circulation at any given time can be represented by their rates of release into the circulation and their rates of clearance from the circulation. How long they survive in the circulation is unclear . Clearance mechanisms include endocytosis, micropinocytosis, phagocytosis and membrane fusion [22, 39]. These processes are dependent upon exposed PSGL-1 on platelet-derived EV attaching to P-selectin expressed from the endothelial cell Weibel–Palade bodies and platelets alpha-granules; and upon the phosphatidylserine on their surface with tethering to Tim4 and lactadherin/MFG-E8 [25, 40]. The extent of surface phosphatidyl serine exposure in-vivo prior to ex vivo manipulation is unknown.
Their rates of clearance have acute and chronic patterns of change and appear to be influenced by their cell of origin [22, 41, 42]. The locales of the macrophage-mediated phagocytosis also differ based upon the organ in which the macrophages are anchored [43–45]. Endothelial receptors may also vary from site to site with different organ-specificities, such as the endothelial cell-rich lungs [46, 47].
The total array of activities of the EVs is still under study. They are involved in cell-to-cell communications, transferring their contents to cell types that differ from their cell of origin [9–12]. This affects cell signaling, platelet and leukocyte adhesion to subendothelial matrix, vascular smooth muscle proliferation, inflammation, immune response, thrombosis, angiogenesis and angiocrine activities, and tumor niche formation leading to enhanced tumor implantation on endothelial surfaces [4, 47–55].
Contributions to thrombosis
EVs become anchored to endothelium in two ways. The PSGL-1 from platelet-derived EV attaches to the P-selectin released from Weibel–Palade bodies of the activated endothelial cell and from the platelet-derived α-granules [55, 59–61]. There also appears to be a phosphatidylserine receptor, at least on cultured activated microvascular endothelial cells derived from pulmonary and retinal tissues . CD36, also known as platelet glycoprotein IIIB and IV among other names, is a scavenger receptor that binds several ligands including phosphatidylserine. It is a candidate cellular adhesion molecule for anchoring the EV. This pathway is blocked when the phosphatidylserine as pretreated with annexin V . Subendothelial thrombospondin is another candidate cellular CAM for the exposed phosphatidylserine . Other cellular adhesion molecules with ability to tether the phosphatidylserine exposed on the surface of the EV include Tim4 and lactadherin [25, 26].
EV trigger thrombosis via release of tissue factor they contain, supplementing the tissue factor released from perivascular tissue following endothelial disruption [9, 11, 12, 50, 65]. The released tissue factor is activated by thiol isomerases, with downstream platelet activation and thrombus formation [56, 57, 66, 67]. This has become a target of a new class of anticoagulants . As an example, quercetin-3-rutinoside suppresses this tissue factor activation [56, 68]. Furthermore, the exposed phosphatidylserine is a catalytic surface for assembly of the prothrombinase complex .
Increased thrombin-generating activity has been recorded for EV derived from platelets and monocytes harvested from patients having recurrent thrombosis .
Suppression of tissue factor with anti-tissue factor antibody and the suppression of P-selectin in PSGL-1 knock out mice reduce clot formation [12, 56, 58]. Similarly, drugs with activity in this domain, such as the HMG-CoA reductase inhibitors, suppress the levels of soluble P-selectin and would consequently be expected to reduce the expression of tissue factor [71–74]. Also, the in vitro blockade of the phosphatidylserine on EVs with annexin V or lactadherin (also known as MFG-E8), both of which attach variably to phosphatidylserine, reduces the platelet-derived EVs contribution to thrombin generation [75–78]. These observations are the basis for new clinical studies.
EVs also accelerate fibrin polymerization, supporting the formation of denser clots that are more resistant to fibrinolysis by tissue plasminogen activator (tPA). Platelet-derived EV also attach to the fibrin fibers [79, 80]. When EVs are removed from the test sample the final clot formation is slowed, with reduced fibrin polymerization leading to increased fibrinolysis in response to added tPA .
Extracellular vesicles and malignancies
The complex relationship of EV and cancers is under investigation. These investigations point roles of EV in the metastatic process, cancer progression, drug- and radiotherapy-resistance and in cancer-related hypercoagulation [16, 48, 52–54, 81–86].
EVs derived from ovarian cancer, prostate cancer and fibrosarcoma paradoxically have the potential of potentiating fibrinolysis [8, 87–92]. The EV-associated urokinase plasminogen activator appears capable of promoting invasion of prostate cancer . The EVs that are shed during blood storage loose their fibrinolytic capacity the longer the red cells are stored . It is not yet known how these findings fit into in vivo clotting/fibrinolytic balance or for the metastatic process.
Activated platelets interact with cancer cells by way of P-selectin and the cancer PSGL-1 expressed on malignant cells . Platelet-derived EV promotes tumor growth and tumor-induced angiogenesis [94, 95]. Melanoma cells release exosomes that change the local and systemic microenvironment so as to better support tumor growth and metastasis [52, 54]. They prepare the sentinel lymph node to trap and support growth of the incoming metastatic melanoma cells by inducing lymphangiogenesis in preparation of a premetastatic niche [53, 96]. This process is dependent upon transmembrane proteins. The tetraspanin-integrin complex contributes to the binding of exosomes to their target cells, possibly mediated by P-selectin/PSGL-1 complex [96–99].
As discussed above, tissue factor is activated by protein disulfide isomerases (PDI) [56, 100–104]. It is also known that many cancers are dependent upon protein disulfide isomerase for survival and metastasis . Thus PDI inhibitors may serve both as anticoagulant and as tumor suppressant .
The EVs derived from cancer cells appear to carry some specific physiologic activities, including the increased tissue factor [6, 11, 106–115]. This blood-borne tissue factor may contribute to the hypercoagulation syndrome that accompanies many cancers [6, 110, 113–117]. The amount of tissue factor-positive EV correlates with venous thrombosis seen in patients with cancer [7, 113–116]. In another study epithelial cancer cells adopted mesenchymal features upon exposure to activated epithelial growth fact receptor coupled with blockade of E-cadherin, leading to a surge of released EV-containing epidermal growth factor receptor (EGFR) and tissue factor . Upon transfer of the tissue factor to cultured endothelial cells, they become procoagulant [11, 117]. Cancer cell-derived EV carrying PSGL-1 can accelerate thrombus formation in vivo by aggregating platelets via the tissue factor-dependent pathway. Their intact parent cells do not have the same capacity [113, 114]. When microparticles derived from tumor cell are injected into mice acute thrombocytopenia and signs of shock follow. This was prevented by prior heparinization . When exposed to hypoxic conditions tumor cell-derived EVs demonstrate the potential for increasing angiogenesis and facilitating metastasis, leading to changes in cell–cell and cell-extracellular matrix interaction allowing for increased invasiveness .
Further exploration of extracellular vesicle activity on vascular endothelium
As demonstrated with phage display, endothelium expresses different receptors depending upon their organ of origin and their functional status [121–125]. This phenomenon has been nicknamed endothelial ZIP codes . This may have therapeutic implications.
Endothelial dysfunction occurs with many pathological states, including sepsis, thrombotic thrombocytopenia purpura, pulmonary hypertension, sickle cell diseases, activation of the complement C5-9 membrane attack complex and exposure to cytotoxic chemotherapy among others [108–110]. These result in changes of phenotype for thrombo-resistance including decreased production of thrombomodulin, tissue-derived plasminogen activator (tPA), heparan sulfate, plasminogen activator inhibitor-1 (PAI-1), but also increased expression of selectins, including over expression of P-selectin from the Weibel–Palade bodies thus leading increased production of procoagulant activity . The over expression of P-selectin facilitates further attachment of EV allowing for further expression of its tissue factor.
The family of selectins and their ligands play roles in the metastatic process and possibly organ selectivity for metastasis. P-selectin facilitates the initial attachment, with subsequent other cellular adhesion molecules (CAMs) furthering the process, including interaction with platelet- and fibrinogen-causing clots with further anchoring of circulating malignant cells [127–131]. Increased adhesion for monocytes and leukocytes further accelerate the clotting process, leading to increased endothelial cell apoptosis and shear-induced endothelial cell loss causing exposure of subendothelial substances .
The angiocrinic function of endothelial cells has been reviewed describing its influence upon tumor growth, as well as organ regeneration and differentiation . The endothelial cells preserve specific niches useful for selective stem cell implantation. This process is associated with inhibitory or stimulatory activities that effect downstream trophagens and cytokines that in turn regulate adoptive healing and metastatic processes [52, 54, 95, 119, 120, 133].
Vascular ligand–receptor mapping
Combinatorial screenings with phage display can be used to identify peptides and proteins with high affinity and specificity for EV [137, 138]. The technique has been used to examine ligand–receptor interactions on the endothelial cells of blood vessels allowing selection of peptides that bind specifically to different vascular beds [123, 138–141]. This technique has been used for unbiased mapping of vascular diversity, the vascular ZIP codes [142, 143]. These ZIP codes are conceived to be the basis for specific ligand delivery on intravascular endothelium. Furthermore, it is conceived that these ZIP codes may vary in certain diseases, including cancers [142, 143]. They are evolving into site-specific targets for drug delivery for prevention of metastatic cell deposits and for the treatment of cancers [141, 142].
It appears possible that phosphatidyl serine receptor-mediated actions as assayed using the ZIP code identification may allow detection of differences in the receptor density based upon source of the endothelial cells and thus differences of EV adherence to those cells. This may add to our understanding of why certain veins are more likely to anchor circulating malignant cells and/or serve as a more effective platform have thrombosis.
Blocking EV function
Creating agents that specifically interfere with the activity of selectin or their ligands is a major area of pharmacologic study . Among already available agents are the HMG-CoA reductase inhibitors that reduce expression of P-selectin so as to reduce anchoring of EVs to the venous endothelium [76–81, 145]. Therapy with statin agents interferes with platelet microparticle (EV) attachment, seemingly causing a fall in the tissue factor expression and subsequent thrombin generation [79, 81, 145]. This may become a model for therapies in other diseases wherein EV play facilitating roles. Another example is a novel recombinant homodimer of annexin V, Diannexin, which binds to and shields phosphatidylserine thereby suppressing phosphatidylserine-mediated leukocyte and platelet attachments . It has been used with success in animal models for preventing reperfusion injury after transplants of lung, muscle, kidney, liver, and islet cell transplants, and following myocardial infarct [147–151]. Quercetin-3-rutinoside blocks EV-related tissue factor activation and platelet aggregation. This latter agent may become a new class of anticoagulant [56, 105]. These same agents may reduce the potential of other EV functions, thus suppressing metastatic cell anchorage and tumor-related angiogenesis. Agents that block Tim4 activity, such as anti-Tim4 antibody, may have future roles, as may anti-P-selectin and P-selectin glycoprotein ligand -1 antibodies .
While some details are known about the roles of circulating EV’s in the complex physiologic and pathophysiologic activities of endothelium there is much yet to be examined. It may be instructive to determine if EV from different source cells adhere to different organ-sourced endothelial cells with different densities and with differing endothelial cell response. It is unknown whether there is a steady state of microparticle attachment to endothelial surfaces in normal circumstances. Are there differences of any such density of adherence depending upon the site of origin of these veins? Is there an accelerated adherence of these particles in disease states that effect endothelial function and integrity? Is there enough of a difference in this density to explain difference in the rates of deep vein thrombosis in certain vessels and the placement of malignant masses in certain vessels but not others? Whether there are specific receptors that facilitate the incorporation of the EV’s membranous and submembranous contents into the interior of the adherent cells is another area in need of further study. Can cancer-derived EV facilitate the initiation of tumor metastasis cascade more efficiently than do intact circulating tumor cells?
The author declares no competing interests.
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- Lötvall J, Hill AF, Hochberg F, Buzás EI, Di Vizio D, Gardiner C et al (2014) Minimal experimental requirements for definition of extracellular vesicles and their functions: a position statement from the International Society for Extracellular Vesicles. J Extracell Vesicles 3:26913. doi:10.3402/jev.v3.26913 PubMedView ArticleGoogle Scholar
- Mathivanan S, Ji H, Simpson RJ (2010) Exosomes: extracellular organelles important in intercellular communication. J Proteom 10(73):1907–1920. doi:10.1016/j.jprot.2010.06.006 View ArticleGoogle Scholar
- Kreimer S, Belov AM, Ghiran I, Murthy SK, Frank DA, Ivanov AR (2015) Mass-spectrometry-based molecular characterization of extracellular vesicles: lipidomics and proteomics. J Proteome Res 14:2367–2384. doi:10.1021/pr501279t PubMedView ArticleGoogle Scholar
- Vlassov AV, Magdaleno S, Setterquist R, Conrad R (2012) Exosomes: current knowledge of their composition, biological functions, and diagnostic and therapeutic potentials. Biochim Biophys Acta 1820:940–948. doi:10.1016/j.bbagen.2012.03.017 PubMedView ArticleGoogle Scholar
- van der Pol E, Böing AN, Gool EL, Nieuwland R (2016) Recent developments in the nomenclature, presence, isolation, detection and clinical impact of extracellular vesicles. J Thromb Haemost 14:48–56. doi:10.1111/jth.13190 PubMedView ArticleGoogle Scholar
- Zahra S, Anderson JA, Stirling D, Ludlam CA (2011) Microparticles, malignancy and thrombosis. Br J Haematol 152:688–700. doi:10.1111/j.1365-2141.2010.08452.x PubMedView ArticleGoogle Scholar
- Zwicker JI, Trenor CC 3rd, Furie BC, Furie B (2011) Tissue factor-bearing microparticles and thrombus formation. Arterioscler Thromb Vasc Biol 31:728–733. doi:10.1161/ATVBAHA.109.200964 PubMedView ArticleGoogle Scholar
- Lacroix R, Dignat-George F (2012) Microparticles as a circulating source of procoagulant and fibrinolytic activities in the circulation. Thromb Res 129(Suppl):27–29. doi:10.1016/j.thromres.2012.02.025 View ArticleGoogle Scholar
- Hussein MA, Böing AN, Biró E, Hoek FJ, Vogel GM, Meuleman DG et al (2008) Phospholipid composition of in vitro endothelial microparticles and their in vivo thrombogenic properties. Thromb Res 121:865–871View ArticleGoogle Scholar
- Vickers KC, Remaley AT (2012) Lipid-based carriers of microRNAs and intercellular communication. Curr Opin Lipidol 23:91–97. doi:10.1097/MOL.0b013e328350a425 PubMedView ArticleGoogle Scholar
- Collier ME, Mah PM, Xiao Y, Maraveyas A, Ettelair C (2013) Microparticle-associated tissue factor is recycled by endothelial cells resulting in enhanced surface tissue factor activity. Thromb Haemost 110:966–976. doi:10.1160/TH13-01-0055 PubMedView ArticleGoogle Scholar
- Falati S, Liu Q, Gross P, Merrill-Skoloff G, Chou J, Vandendries E et al (2003) Accumulation of tissue factor into developing thrombi in vivo is dependent upon microparticle P-selectin glycoprotein ligand 1 and platelet P-selectin. J Exp Med 197:1585–1598PubMedPubMed CentralView ArticleGoogle Scholar
- Hrachovinová I, Cambien B, Hafezi-Moghadam A, Kappelmayer J, Camphausen RT, Widom A et al (2003) Interaction of P-selectin and PSGL-1 generates microparticles that correct hemostasis in a mouse model of hemophilia A. Nat Med 9:1020–1025PubMedView ArticleGoogle Scholar
- Hannun YA, Obeid LM (2011) Many ceramides. J Biol Chem 286:27855–27862. doi:10.1074/jbc.R111.254359 PubMedPubMed CentralView ArticleGoogle Scholar
- Valadi H, Ekström K, Bossios A, Sjöstrand M, Lee JJ, Lötvall JO (2007) Exosome-mediated transfer of mRNAs and microRNA is a novel mechanism of genetic exchange between cells. Nat Cell Biol 9:654–659. doi:10.1038/ncb1596 PubMedView ArticleGoogle Scholar
- Thakur BK, Zhang H, Becker A, Matei I, Huang Y, Costa-Silva B et al (2014) Double-stranded DNA in exosomes: a novel biomarker in cancer detection. Cell Res 24:766–769. doi:10.1038/cr.2014.44 PubMedPubMed CentralView ArticleGoogle Scholar
- Zomer A, Vendrig T, Hopmans ES, von Eijndhoven M, Middeldorp JM, Pegtel DM (2010) Exosomes: fit to deliver small RNA. Commun Integr Biol 3:447–450. doi:10.4161/cib.3.5.12339 PubMedPubMed CentralView ArticleGoogle Scholar
- Gustafson CM, Shepherd AJ, Miller VM, Jayachandran M (2015) Age- and sex-specific differences in blood-borne microvesicles from apparently healthy humans. Biol Sex Differ 6:10. doi:10.1186/s13293-015-0028-8 PubMedPubMed CentralView ArticleGoogle Scholar
- Rautou PE, Mackman N (2013) Microvesicles as risk markers for venous thrombosis. Exp Rev Hematol 6:91–101. doi:10.1586/ehm.12.74 View ArticleGoogle Scholar
- Herring JM, McMichael MA, Smith SA (2013) Microparticles in health and disease. J Vet Intern Med 27:1020–1033. doi:10.1111/jvim.12128 PubMedView ArticleGoogle Scholar
- Cocucci E, Racchetti J, Meldolesi J (2009) Shedding microvesicles: artifacts no more. Trends Cell Biol 19:43–51. doi:10.1016/j.tcb.2008.11.003 PubMedView ArticleGoogle Scholar
- Ayers L, Nieuwland R, Kohler M, Kraenkel N, Ferry B, Leeson P (2015) Dynamic microvesicle release and clearance within the cardiovascular system: triggers and mechanisms. Clin Sci 129:915–931. doi:10.1016/j.tcb.2008.11.003 PubMedView ArticleGoogle Scholar
- Johnstone RM, Mathew A, Mason AB, Teng K (1991) Exosome formation during maturation of mammalian and avian reticulocytes: evidence that exosome release is a major route for externalization of obsolete membrane proteins. J Cell Physiol 147:27–36PubMedView ArticleGoogle Scholar
- Stace CL, Ktistakis NT (2006) Phosphatidic acid- and phosphatidylserine-binding proteins. Biochem Biophys Acta 1761:913–926PubMedGoogle Scholar
- Ye H, Li B, Subramanian V, Choi BH, Liang Y, Harikishore A et al (2013) NMR solution structure of C2 domain of MFG-E8 and insights into its molecular recognition with phosphatidylserine. Biochim Biophys Acta 1828:1083–1093. doi:10.1016/j.bbamem.2012.12.009 PubMedView ArticleGoogle Scholar
- Tietjen GT, Gong Z, Chen CH, Vargas E, Crooks JE, Cao KD et al (2014) Molecular mechanism for differential recognition of membrane phosphatidylserine by the immune regulatory receptor Tim4. Proc Natl Acad Sci USA 111:E1463–E1472. doi:10.1073/pnas.1320174111 PubMedPubMed CentralView ArticleGoogle Scholar
- Ludwig A, Giebel B (2012) Exosomes: small vesicles participating in intercellular communication. Int J Biochem Cell Biol 44:11–15. doi:10.1016/j.biocel.2011.10.005 PubMedView ArticleGoogle Scholar
- Li XB, Zhang ZR, Schluesener HJ, Xu SQ (2006) Role of exosomes in immune regulation. J Cell Mol Med 10:364–375. doi:10.1111/j.1582-4934.2006.tb00405.x PubMedView ArticleGoogle Scholar
- Hauser P, Wang S, Didenka W (2017) Apoptotic bodies: selective detection in extracellular vesicles. Methods Mol Biol 1554:193–200. doi:10.1007/978-1-4939-6759-9_12 PubMedView ArticleGoogle Scholar
- Muller L, Hong CS, Stolz DB, Watkins SC, Whiteside TL (2014) Isolation of biologically-active exosomes from human plasma. J Immunol Methods 411:55–65. doi:10.1016/j.jim.2014.06.007 PubMedPubMed CentralView ArticleGoogle Scholar
- Lacroix R, Judicone C, Poncelet P, Rovert S, Arnaud L, Sampol J et al (2012) Impact of pre-analytical parameters on the measurement of circulating microparticles: towards standardization of protocol. J Thromb Haemost 10:437–446. doi:10.1111/j.1538-7836.2011.04610.x PubMedView ArticleGoogle Scholar
- Januszyk K, Lima CD (2010) Structural components and architectures of RNA exosomes. Adv Exp Med Biol 702:9–28PubMedPubMed CentralView ArticleGoogle Scholar
- Poncelet P, Robert S, Bailly N, Garnache-Ottou F, Bouriche T, Devalet B, Segatchian JH et al (2015) Tips and tricks for flow cytometry-based analysis and counting of microparticles. Transfus Apher Sci 53:110–126. doi:10.1016/j.transci.2015.10.008 PubMedView ArticleGoogle Scholar
- Nakai W, Yoshida T, Diez D, Miyatake Y, Nishibu T, Imawaka N et al (2016) A novel affinity-based method for the isolation of highly purified extracellular vesicles. Sci Rep 6(33935):1–11. doi:10.1038/srep33935 Google Scholar
- Miyanishi M, Tada K, Koike M, Uchiyama Y, Kitamura T, Nagata S et al (2007) Identification of Tim4 as a phosphatidylserine receptor. Nature 450:435–439PubMedView ArticleGoogle Scholar
- Moreno-Gonzalo O, Villarroya-Beltri C, Sánchez-Madrid F (2014) Post-translational modifications of exosomal proteins. Front Immunol 5:383. doi:10.3389/fimmu.2014.00383 PubMedPubMed CentralView ArticleGoogle Scholar
- Szabó-Taylor K, Ryan B, Osteikoetxea X, Szabó TG, Sódar B, Holub M et al (2015) Oxidative and other posttranslational modifications in extracellular vesicle biology. Semin Cell Dev Biol 40:8–16. doi:10.1016/j.semcdb.2015.02.012 PubMedView ArticleGoogle Scholar
- Charrin S, Manie S, Oualid M, Billard M, Boucheix C, Rubinstein E (2002) Differential stability of tetraspanin–tetraspanin interactions: role of palmitoylation. FEBS Lett 516:139–144PubMedView ArticleGoogle Scholar
- Henson PM, Bratton DL, Fadok VA (2001) Apoptotic cell removal. Curr Biol 11:R795–R805PubMedView ArticleGoogle Scholar
- Zhang Y, Meng H, Ma R, He Z, Wu X, Cao M et al (2016) Circulating microparticles, blood cells, and endothelium induce procoagulant activity in sepsis through phosphatidylserine exposure. Shock 45:299–307. doi:10.1097/SHK.0000000000000509 PubMedView ArticleGoogle Scholar
- Jansen F, Yang X, Hoyer FF, Paul K, Heiermann N, Becher MU et al (2012) Endothelial microparticle uptake in target cells in annexin 1/phosphatidylserine receptor dependent and prevents apoptosis. Arterioscler Thromb Vasc Biol 32:1925–1935. doi:10.1161/ATVBAHA.112.253229 PubMedView ArticleGoogle Scholar
- Brown S, Heinisch I, Ross E, Shaw K, Buckley CD, Savill J (2002) Apoptosis disables CD31-mediated cell detachment from phagocytes promoting binding and engulfment. Nature 418:200–203PubMedView ArticleGoogle Scholar
- Dasgupta SK, Abdel-Monem H, Niravath P, Le A, Bellera RV, Langlois K (2009) Lactadherin and clearance of platelet-derived microvesicles. Blood 113:1332–1339. doi:10.1182/blood-2008-07-167148 PubMedPubMed CentralView ArticleGoogle Scholar
- Willekens F, Werre JM, Kruijt JK, Roerdinkholder-Stoelwinder B, Groenen-Döpp YA, van den Bos AG et al (2005) Liver Kupffer cells rapidly remove red blood cell-derived vesicles from the circulation by scavenger receptors. Blood 105:2141–2145PubMedView ArticleGoogle Scholar
- Al Faraj A, Gazeau F, Wilhelm C, Devue C, Guérin CL, Péchoux C et al (2012) Endothelial cell-derived microparticles loaded with iron oxide nanoparticles: feasibility of MR imaging monitoring in mice. Radiology 263:169–178. doi:10.1148/radiol.11111329 PubMedView ArticleGoogle Scholar
- Qiu Q, Xiong W, Yang C, Gagnon C, Hardy P (2013) Lymphocyte-derived microparticles induce bronchial epithelial cells’ pro-inflammatory cytokine production and apoptosis. Mol Immunol 55:220–230. doi:10.1016/j.molimm.2013.01.017 PubMedView ArticleGoogle Scholar
- Bastarache JA, Fremont RD, Kropski JA, Bossert FR, Ware LB (2009) Procoagulant alveolar microparticles in the lung of patients with acute respiratory distress syndrome. Am J Physiol Lung Cell Mol Physiol 297:L1035–L1041. doi:10.1152/ajplung.00214.2009 PubMedPubMed CentralView ArticleGoogle Scholar
- Janowska-Wieczorek A, Wysoczynski M, Kijowski J, Marquez-Curtis L, Machalinski B, Ratajczak J et al (2005) Microvesicles derived from activated platelets induce metastasis and angiogenesis in lung cancer. Int J Cancer 113:752–760PubMedView ArticleGoogle Scholar
- Furie B, Furie BC (2005) Thrombosis formation in vivo. J Clin Investig 115:3355–3362PubMedPubMed CentralView ArticleGoogle Scholar
- Chou J, Mackman N, Merrill-Skoloff G, Pederson B, Furie BC, Furie B (2004) Hematopoietic cell-derived microparticle tissue factor contributes to fibrin formation during thrombus propagation. Blood 104:3190–3197PubMedView ArticleGoogle Scholar
- Simoncini S, Njock MS, Robert S, Camoin-Jau L, Sampol J, Harlé JR et al (2009) TRAIL/Apo2L mediates the release of procoagulant endothelial microparticles induced by thrombin in vitro. A potential mechanism linking inflammation and coagulation. Circ Res 104:943–951. doi:10.1161/CIRCRESAHA.108.183285 PubMedView ArticleGoogle Scholar
- Kahlert C, Kalluri R (2013) Exosomes in tumor microenvironment influence cancer progression and metastasis. J Mol Med 91:431–437. doi:10.1007/s00109-013-1020-6 PubMedPubMed CentralView ArticleGoogle Scholar
- Hood JL, San RS, Wickline SA (2011) Exosomes released by melanoma cells prepare sentinel lymph nodes for tumor metastasis. Cancer Res 71:3792–3801. doi:10.1158/0008-5472 PubMedView ArticleGoogle Scholar
- Rinderknecht M, Detmar M (2008) Tumor lymphangiogenesis and melanoma metastasis. J Cell Physiol 216:347–354. doi:10.1002/jcp.21494 PubMedView ArticleGoogle Scholar
- Cambien B, Wagner DD (2004) A new role in hemostasis for the adhesion receptor P-selectin. Trends Mol Med 10:179–186PubMedView ArticleGoogle Scholar
- Furie B, Flaumenhaft R (2014) Thiol isomerases in thrombus formation. Clin Res 114:1162–1173. doi:10.1161/CIRCRESAHA.114.301808 Google Scholar
- Zhou L, Qi XL, Xu MX, Mao Y, Liu ML, Song HM (2014) Microparticles: new light shed on the understanding of venous thromboembolism. Acta Pharmacol Sin 35:1103–1110. doi:10.1038/aps.2014.73 PubMedPubMed CentralView ArticleGoogle Scholar
- Furie B, Furie BC (2004) Role of platelet P-selectin and microparticle PSGL-1 in thrombus formation. Trends Mol Med 10:171–178PubMedView ArticleGoogle Scholar
- Vandendries ER, Furie BC, Furie B (2004) Role of P-selectin and PSGL-I in coagulation and thrombosis. Thromb Haemost 92:459–466PubMedGoogle Scholar
- McEver RP, Beckstead JH, Moore KL, Marshall-Carlson L, Bainton DF (1989) GMP-140, a platelet alpha-granule membrane protein, is also synthesized by vascular endothelial cells and is localized in Weibel–Palade bodies. J Clin Investig 84:92–99PubMedPubMed CentralView ArticleGoogle Scholar
- Montoro-Garcia S, Shantsila E, Hermández-Romero D, Jover E, Valdés M, Marin F et al (2014) Small-size platelet microparticles trigger platelet and monocyte functionality and modulate thrombogenesis via P-selectin. Br J Haematol 166:571–580. doi:10.1111/bjh.12913 PubMedView ArticleGoogle Scholar
- Setty BN, Betal SG (2008) Microvascular endothelial cells express a phosphatidylserine receptor: a functionally active receptor for phosphatidylserine-positive erythrocytes. Blood 111:905–914PubMedPubMed CentralView ArticleGoogle Scholar
- Lopez-Vilchez I, Diaz-Ricart M, Galan AM, Roque M, Caballo C, Molina P et al (2016) Internalization of tissue factor-rich microvesicles by platelets occurs independently of GPIIb-IIIa, and involves CD36 receptor, serotonin transporter and cytoskeletal assembly. J Cell Biochem 117:448–457. doi:10.1002/jcb.25293 PubMedView ArticleGoogle Scholar
- Manodori AB, Barabino GA, Lubin BH, Kuypers FA (2000) Adherence of phosphatidylserine-exposing erythrocytes to endothelial matrix thrombospondin. Blood 95:1293–1300PubMedGoogle Scholar
- Sabatier F, Roux V, Anfosso F, Camoin L, Sampol J, Dignat-George F (2002) Interaction of endothelial microparticles with monocytic cells in vitro induces tissue factor-dependent procoagulant activity. Blood 99:3962–3970PubMedView ArticleGoogle Scholar
- Furie B, Furie BC, Flaumenhaft R, Zwicker JI (2014) Animal models of arterial and venous thrombosis. Blood 124:SCI 2View ArticleGoogle Scholar
- Reinhardt C, von Brühl ML, Manukyan D, Grahl L, Lorenz M, Altmann B et al (2008) Protein disulfide isomerase acts as an injury response signal that enhances fibrin generation via tissue factor activation. J Clin Investig 118:1110–1122. doi:10.1172/JCI32376 PubMedPubMed CentralGoogle Scholar
- Jasuja R, Passam FH, Kennedy DR, Kim SH, van Hessem L, Lin L et al (2012) Protein disulfide isomerase inhibitors constitute a new class of antithrombotic agents. J Clin Investig 122:2104–2113. doi:10.1172/JCI61228 PubMedPubMed CentralView ArticleGoogle Scholar
- Hamilton KK, Hattori R, Esmon CT, Sims PJ (1990) Complement proteins C5b-9 induce vesiculation of the endothelial plasma membrane and expose catalytic surface for the assembly of the prothrombinase enzyme complex. J Biol Chem 265:3809–3814PubMedGoogle Scholar
- Bidot L, Jy W, Bidot C Jr, Jimenez JJ, Fontana V, Horstman LL et al (2008) Microparticle-mediated thrombin generation assay: increased activity in patients with recurrent thrombosis. J Thromb Haemost 6:913–919. doi:10.1111/j.1538-7836.2008.02963.x PubMedView ArticleGoogle Scholar
- Mobarrez F, He S, Bröijersen A, Wiklund B, Antovic A, Antovic J et al (2011) Atrovastatin reduces thrombin generation and expression of tissue factor, P-selectin and GPIIIa on platelet-derived microparticles in patients with peripheral arterial occlusive disease. Thromb Haemost 106:344–352. doi:10.1160/TH10-12-0810 PubMedView ArticleGoogle Scholar
- Romano M, Mezzetti A, Marulli C, Ciabattoni G, Febo F, Di Ienno S et al (2000) Fluvastatin reduces soluble P-selectin and ICAM-1 levels on hypercholesterolemic patients: role of nitric oxide. J Investig Med 48:183–189PubMedGoogle Scholar
- Berkan O, Katrancioglu N, Ozker E, Ozerdem G, Bakici Z, Yilmaz MB (2009) Reduced P-selectin in hearts pretreated with fluvastatin: a novel benefit for patients undergoing open heart surgery. Thorac Cardiovasc Surg 57:91–95. doi:10.1055/s-2008-1039107 PubMedView ArticleGoogle Scholar
- Mobarrez F, Egberg N, Antovic J, Bröijersen A, Jörenkog G, Wallén H (2012) Release of endothelial microparticles in vivo during atorvastatin treatment; a randomized double blind placebo-controlled study. Thromb Res 129:95–97. doi:10.1016/j.thromres.2011.09.027 PubMedView ArticleGoogle Scholar
- Connor DE, Exner T, Ma DD, Josepth JE (2010) The majority of circulating platelet-derived microparticles fail to bind annexin V, lack phospholipid-dependent procoagulant activity and demonstrate greater expression of glycoprotein 1B. Thromb Haemost 103:1044–1052. doi:10.1160/TH09-09-0644 PubMedView ArticleGoogle Scholar
- Ravanat C, Archipoff G, Beretz A, Freund G, Cazenave JP, Freyssinet JM (1992) Use of annexin-V to demonstrate the role of phosphatidylserine exposure in the maintenance of haemostatic balance by endothelial cells. Biochem J 282:7–13PubMedPubMed CentralView ArticleGoogle Scholar
- Albanyan AM, Murphy MF, Rasmussen JT, Heegaard CW, Harrison P (2009) Measurement of phosphatidylserine exposure during storage of platelet concentrates using the novel probe lactadherin: a comparison study with annexin V. Transfusion 49:99–107. doi:10.1111/j.1537-2995.2008.01933.x PubMedView ArticleGoogle Scholar
- Ravassa S, Bennaghmouch A, Kenis H, Lindhout T, Hackeng T, Narula J et al (2005) Annexin A5 down-regulates surface expression of tissue factor: a novel mechanism of regulating the membrane receptor repertoir. J Biol Chem 280:6028–6035PubMedView ArticleGoogle Scholar
- Zubairova LD, Nabiulina RM, Nagaswami C, Zuev YE, Mustafin IG, Litvinov RI et al (2015) Circulating microparticles alter formation, structure, and properties of fibrin clots. Sci Rep 5:17611. doi:10.1038/srep17611 PubMedPubMed CentralView ArticleGoogle Scholar
- Nabiullina RM, Mustafin IG, Zuev YF, Faizullin DA, Litvinov RI, Zubairova LD (2015) Effect of blood microparticles on the kinetics of polymerization and enzymatic hydrolysis of fibrin. Dokl Biochem Biophys 462:151–154. doi:10.1134/S1607672915030035 PubMedView ArticleGoogle Scholar
- Milane L, Singh A, Mattheolabakis G, Suresh M, Amiji MM (2015) Exosome mediated communication within the tumor microenvironment. J Control Release 219:278–294. doi:10.1016/j.jconrel.2015.06.029 PubMedView ArticleGoogle Scholar
- Brinton LT, Sloane HS, Kester M, Kelly KA (2015) Formation and role of exosomes in cancer. Cell Mol Life Sci 72:659–671. doi:10.1007/s00018-014-1764-3 PubMedView ArticleGoogle Scholar
- Chin AR, Wang SE (2016) Cancer-derived extracellular vesicles: the ‘soil conditioner’ in breast cancer metastasis. Cancer Metastasis Rev 35:669–676. doi:10.1007/s10555-016-9639-8 PubMedView ArticleGoogle Scholar
- Suchorska WM, Lach MS (2016) The role of exosomes in tumor progression and metastasis. Oncol Rep 25:1237–1244. doi:10.3892/or.2015.4507 Google Scholar
- Pultz BDA, Luz FAC, Faria SS, Souza LPF, Tavares PCB, Goulart VA et al (2017) The multifaceted role of extracellular vesicles in metastasis: priming the soil for seeding. Int J Cancer 140:2397–2407. doi:10.1002/ijc.30595 View ArticleGoogle Scholar
- Lobb RJ, van Amerongen R, Wiegmans A, Ham S, Larsen JE, Möller A (2017) Exosomes derived from mesenchymal non-small cell lung cancer cells promote chemoresistance. Int J Cancer 141:614–620. doi:10.1002/ijc.30752 PubMedView ArticleGoogle Scholar
- Dolo V, D’Ascenzo S, Violini S, Pompucci L, Festuccia C, Ginestra A et al (1999) Matrix-degrading proteinases are shed in membrane vesicles by ovarian cancer cells in vivo and in vitro. Clin Exp Metastasis 17:131–140PubMedView ArticleGoogle Scholar
- Ginestra A, Monea S, Seghezzi G, Dolo V, Nagase H, Mignatti P et al (1997) Urokinase plasminogen activator and gelatinases are associated with membrane vesicles shed by human HT1080 fibrosarcoma cells. J Biol Chem 272:17216–17222PubMedView ArticleGoogle Scholar
- Angelucci A, D’Ascenzo S, Festuccia C, Gravina GL, Bologa M, Dolo V et al (2000) Vesicle-associated urokinase plasminogen activator promotes invasion in prostate cancer cells lines. Clin Exp Metastasis 18:163–170PubMedView ArticleGoogle Scholar
- Brodsky SV, Malinowski K, Golightly M, Jesty J, Goligorsky MS (2002) Plasminogen activator inhibitor-I promotes formation of endothelial microparticles with procoagulant potential. Circulation 106:2372–2378PubMedView ArticleGoogle Scholar
- Lacroix R, Sabatier F, Mialhe A, Basire A, Pannell R, Borghi H et al (2007) Activation of plasminogen into plasmin at the surface of endothelial microparticles: a mechanism that modulates angiogenic properties of endothelial progenitor cells in vitro. Blood 110:2432–2439PubMedPubMed CentralView ArticleGoogle Scholar
- Levin G, Sukhareva E, Lavrentieva A (2016) Impact of microparticles derived from erythrocytes on fibrinolysis. J Thromb Thrombolysis 41:452–458. doi:10.1007/s11239-015-1299-y PubMedView ArticleGoogle Scholar
- Gong L, Cai Y, Zhou X, Yang H (2012) Activated platelets interact with lung cancer cells through P-selectin glycoprotein ligand-1. Pathol Oncol Res 18:989–996. doi:10.1007/s12253-012-9531-y PubMedView ArticleGoogle Scholar
- Goubran H, Sabry W, Kolb R, Seghatchian J, Burnouf T (2015) Platelet microparticles and cancer: an intimate cross-talk. Transfus Apher Sci 53:168–172. doi:10.1016/j.transci.2015.10.014 PubMedView ArticleGoogle Scholar
- Sierko E, Wojtukiewicz MZ (2004) Platelets and angiogenesis in malignancy. Semin Thromb Hemost 30:95–108PubMedView ArticleGoogle Scholar
- Hood JL, Pan H, Lanza GM, Wickline SA (2009) Consortium for translational research in advanced imaging and nanomedicine (C-TRAIN) paracrine induction of endothelium by tumor exosomes. Lab Investig 89:1317–1328. doi:10.1038/labinvest.2009.94 PubMedPubMed CentralView ArticleGoogle Scholar
- Nazarenko I, Rana S, Baumann A, McAlear J, Hellwig A, Trendelenburg M et al (2010) Cell surface tetraspanin Tspan8 contributes to molecular pathways of exosome-induced endothelial cell activation. Cancer Res 70:1668–1678. doi:10.1158/0008-5472.CAN-09-2470 PubMedView ArticleGoogle Scholar
- Rana S, Yue S, Stadel D, Zoller M (2012) Toward tailored exosomes: the exosomal tetraspanin web contributes to target cell selection. Int J Biochem Cell Biol 44:1574–1584. doi:10.1016/jbiocel.2012.06.018 PubMedView ArticleGoogle Scholar
- Chen M, Geng JG (2006) P-selectin mediates adhesion of leukocytes, platelets, and cancer cells in inflammation, thrombosis, and cancer growth and metastasis. Arch Immunol Ther Exp 54:75–84. doi:10.1007/s00005-006-0010-6 View ArticleGoogle Scholar
- Cho J, Furie BC, Coughlin SR, Furie B (2008) A critical role for extracellular protein disulfide isomerase during thrombus formation in mice. J Clin Investig 118:1123–1131. doi:10.1172/JCI34134 PubMedPubMed CentralGoogle Scholar
- Flaumenhaft R, Furie B (2016) Vascular thiol isomerases. Blood 128:893–901. doi:10.1182/blood-2016-04-636456 PubMedPubMed CentralView ArticleGoogle Scholar
- Chen VM (2013) Tissue factor de-encryption, thrombus formation, and thiol-disulfide exchange. Semin Thromb Hemost 39:40–47. doi:10.1055/s-0032-1333311 PubMedView ArticleGoogle Scholar
- Schulman S, Bendapudi P, Sharda A, Chen V, Bellido-Martin L, Jasuja R et al (2016) Extracellular thiol isomerases and their role in thrombus formation. Antioxid Redox Signal 24:1–15. doi:10.1089/ars.2015.6530 PubMedPubMed CentralView ArticleGoogle Scholar
- Ruf W (2012) Role of thiol pathways in TF procoagulant regulation. Thromb Res 129(Suppl 2):11–12. doi:10.1016/j.thromres.2012.02.020 View ArticleGoogle Scholar
- Xu S, Sankar S, Neamati N (2014) Protein disulfide isomerase: a promising target for cancer therapy. Drug Discov Today 19:222–240. doi:10.1016/j.drudis.2013.10.017 PubMedView ArticleGoogle Scholar
- Tesselaar ME, Romijn FP, Van Der Linden IK, Prins FA, Bertina RM, Osanto S (2007) Microparticle-associated tissue factor activity: a link between cancer and thrombosis? J Thromb Haemost 5:520–527PubMedView ArticleGoogle Scholar
- Hron G, Kollars M, Weber H, Sagaster V, Quehenberger P, Eichinger S et al (2007) Tissue factor-positive microparticles: cellular origin and association with coagulation activation in patients with colorectal cancer. Thromb Haemost 97:119–123PubMedGoogle Scholar
- Simák J, Holada K, Vostal JG (2002) Release of annexin V-binding membrane microparticles from cultured human umbilical endothelial cells after treatment with camptothecin. BMC Cell Biol 3:11–21. doi:10.1186/1471-2121-3-11 PubMedPubMed CentralView ArticleGoogle Scholar
- Brunetta DM, De Santis GC, Silva-Pinto AC, Oliveira de Oliveira LC, Covas DT (2015) Hydroxyurea increases plasma concentrations of microparticles and reduces coagulation activation and fibrinolysis in patients with sickle cell disease. Acta Haematol 133:287–294. doi:10.1159/000362148 PubMedView ArticleGoogle Scholar
- Lysov Z, Dwivedi D, Gould TJ, Liaw PC (2017) Procoagulant effects of lung cancer chemotherapy: impact on microparticles and cell-free DNA. Blood Coagul Fibrinolysis 28:72–82. doi:10.1097/MBC.0000000000000546 PubMedView ArticleGoogle Scholar
- Fernandez PM, Rickles FR (2002) Tissue factor and angiogenesis in cancer. Curr Opin Hematol 9:401–406PubMedView ArticleGoogle Scholar
- Bromberg ME, Konigsberg WH, Madison JF, Pawashe A, Garen A (1995) Tissue factor promotes melanoma metastasis by a pathway independent of blood coagulation. Proc Natl Acad Sci USA 92:8205–8209PubMedPubMed CentralView ArticleGoogle Scholar
- Thomas GM, Panicot-Dubois L, Lacroix R, Dignat-George F, Lombardo D, Dubois C (2009) Cancer cell-derived microparticles bearing P-selectin glycoprotein ligand 1 accelerate thrombus formation in vivo. J Exp Med 206:1913–1927. doi:10.1084/jem.20082297 PubMedPubMed CentralView ArticleGoogle Scholar
- Thomas GM, Brill A, Mezouar S, Crescence L, Gallant M, Dubois C et al (2015) Tissue factor expressed by circulating cancer cell-derived microparticles drastically increases the incidence of deep vein thrombosis in mice. J Thromb Haemost 13:1310–1319. doi:10.1111/jth.13002 PubMedPubMed CentralView ArticleGoogle Scholar
- Geddings JE, Mackman N (2013) Tumor-derived tissue factor-positive microparticles and venous thrombosis in cancer patients. Blood 122:1873–1880. doi:10.1182/blood-2013-04-460139 PubMedPubMed CentralView ArticleGoogle Scholar
- Khorana AA, Francis CW, Menzies KE, Wang JG, Hyrien O, Hathcock J et al (2008) Plasma tissue factor may be predictive of venous thromboembolism in pancreatic cancer. J Thromb Haemost 6:1983–1985. doi:10.1111/j.1538-7836.2008.03156.x PubMedPubMed CentralView ArticleGoogle Scholar
- Garnier D, Magnus N, Lee TH, Bentley V, Meehan B, Milsom C et al (2012) Cancer cells induced to express mesenchymal phenotype release exosome-like extracellular vesicles carrying tissue factor. J Biol Chem 287:43565–43572. doi:10.1074/jbc.M112.401760 PubMedPubMed CentralView ArticleGoogle Scholar
- Park JE, Tan HS, Datta A, Lai RC, Zhang H, Meng W et al (2010) Hypoxic tumor cell modulates its microenvironment to enhance angiogenic and metastatic potential by secretion of proteins and exosomes. Mol Cell Proteom 9:1085–1099. doi:10.1074/mcp.M900381-MCP200 View ArticleGoogle Scholar
- Butler JM, Kobayashi H, Rafii S (2010) Instructive role of the vascular niche in promoting tumour growth and tissue repair by angiocrine factors. Nat Rev Cancer 10:138–146. doi:10.1038/nrc2791 PubMedPubMed CentralView ArticleGoogle Scholar
- Rafii S, Butler JM, Ding BS (2016) Angiocrine functions of organ-specific endothelial cells. Nature 529:316–325. doi:10.1038/nature17040 PubMedPubMed CentralView ArticleGoogle Scholar
- Pasqualini R, Ruoslahti E (1996) Organ targeting in vivo using phage display peptide libraries. Nature 380:364–366PubMedView ArticleGoogle Scholar
- Rajotte D, Arap W, Hagedorn M, Koivunen E, Pasqualini R, Ruoslahti E (1998) Molecular heterogeneity of the vascular endothelium revealed by in vivo phage display. J Clin Investig 102:430–437PubMedPubMed CentralView ArticleGoogle Scholar
- Trepel M, Pasqualini R, Arap W (2008) Screening phage-display peptide libraries for vascular targeted peptides. Methods Enzymol 445:83–106. doi:10.1016/S0076-6879(08)03004-8 PubMedView ArticleGoogle Scholar
- Bredesen DE, Pasqualini R, Ruoslahti E (2002) Targeting the prostate for destruction through vascular address. Proc Natl Acad Sci USA 99:1527–1531PubMedPubMed CentralView ArticleGoogle Scholar
- Arap W, Kolonin MG, Trepel M, Lahdenranta J, Cardó-Vila M, Giordano RJ et al (2002) Steps toward mapping the human vasculature by phage display. Nat Med 8:121–127PubMedView ArticleGoogle Scholar
- Ruoslahti E (2004) Vascular zip codes in angiogenesis and metastasis. Biochem Soc Trans 32:397–402. doi:10.1042/BST0320397 PubMedView ArticleGoogle Scholar
- Vallet B, Wiel E (2001) Endothelial cell dysfunction and coagulation. Crit Care Med 29(Suppl 7):36–41View ArticleGoogle Scholar
- Borsig L, Wong R, Feramisco J, Nadeau DR, Varki NM (2001) Varki A Heparin and cancer revisited: mechanistic connections involving platelets, P-selectin, carcinoma mucins, and tumor metastasis. Proc Natl Acad Sci USA 98:3352–3357. doi:10.1073/pnas.061615598 PubMedPubMed CentralView ArticleGoogle Scholar
- Borsig L, Wong R, Hynes RO, Varki NM, Varki A (2002) Synergistic effects of L- and P-selectin in facilitating tumor metastasis can involve non-mucin ligands and implicate leukocytes as enhancers of metastasis. Proc Natl Acad Sci USA 99:2193–2198. doi:10.1073/pnas.261704098 PubMedPubMed CentralView ArticleGoogle Scholar
- Im JH, Fu W, Wang H, Bhatia SK, Hammer DA, Kowalska MA et al (2004) Coagulation facilitates tumor cell spreading in the pulmonary vasculature during early metastatic colony formation. Cancer Res 64:8613–8619PubMedView ArticleGoogle Scholar
- Biggerstaff JP, Seth N, Amirkhosravi A, Amaya M, Fogarty S, Meyer TV et al (1999) Soluble fibrin augments platelet/tumor cell adherence in vitro and in vivo, and enhances experimental metastasis. Clin Exp Metastasis 17:723–730PubMedView ArticleGoogle Scholar
- Bombeli T, Karsan A, Tait JF, Harlan JM (1997) Apoptotic vascular endothelial cells become procoagulant. Blood 89:2429–2442PubMedGoogle Scholar
- Curtis AM, Edelberg J, Jonas R, Rogers WT, Moore JS, Syed W et al (2013) Endothelial microparticles: sophisticated vesicle modulating vascular function. Vasc Med 18:204–214. doi:10.1177/1358863X13499773 PubMedPubMed CentralView ArticleGoogle Scholar
- Walker B, Towhid ST, Schmid E, Hoffmann SM, Abed M, Münzer P et al (2014) Dynamic adhesion of eryptotic erythrocytes to immobilized platelets via platelet phosphatidylserine receptors. Am J Physiol Cell Physiol 306:C291–C297. doi:10.1152/ajpcell.00318.2013 PubMedView ArticleGoogle Scholar
- van Engeland M, Nieland LJ, Ramaekers FC, Schutte B, Reutelingsperger CP (1998) Annexin V-affinity assay: a review on an apoptosis detection system based on phosphatidylserine exposure. Cytometry 31:1–9PubMedView ArticleGoogle Scholar
- van Genderen HO, Kenis H, Hostra L, Narula J, Reutelingsperger CP (2008) Extracellular annexin A5: functions of phosphatidylserine-binding and two-dimensional crystallization. Biochim Biophys Acta 1783:953–963. doi:10.1016/j.bbamcr.2008.01.030 PubMedView ArticleGoogle Scholar
- Christianson DR, Ozawa MG, Pasqualini R, Arap W (2007) Techniques to decipher molecular diversity by phage display. Methods Mol Biol 357:385–406PubMedGoogle Scholar
- Azzazy HM, Highsmith WE Jr (2002) Phage display technology: clinical applications and recent innovations. Clin Biochem 35:425–445PubMedView ArticleGoogle Scholar
- Staquicini FI, Moeller BJ, Arap W, Pasqualini R (2010) Combinatorial vascular targeting in translational medicine. Proteom Clin Appl 4:626–632. doi:10.1002/prca.200900213 View ArticleGoogle Scholar
- Giordano RJ, Edwards JK, Tuder RM, Arap W, Pasqualini R (2009) Combinatorial ligand-directed lung targeting. Proc Am Thorac Soc 6:411–415. doi:10.1513/pats.200903-014AW PubMedPubMed CentralView ArticleGoogle Scholar
- Pasqualini R, Moeller BJ, Arap W (2010) Leveraging molecular heterogeneity of the vascular endothelium for targeted drug delivery and imaging. Semin Thromb Hemost 36:343–351. doi:10.1055/s-0030-1253456 PubMedView ArticleGoogle Scholar
- Li XB, Schluesener HJ, Xu SQ (2006) Molecular addresses of tumors: selection by in vivo phage display. Arch Immunol Ther Exp 54:177–181View ArticleGoogle Scholar
- Staquicini FI, Cardó-Vila M, Kolonin MG, Trepel M, Edwards JK, Nunes DR et al (2011) Vascular ligand-receptor mapping by direct combinatorial selection in cancer patients. Proc Natl Acad Sci 108:18637–18642. doi:10.1073/pnas.1114503108 PubMedPubMed CentralView ArticleGoogle Scholar
- Kneuer C, Ehrhardt C, Radomski MW, Bakowsky U (2006) Selectins-potential pharmacological targets? Drug Discov Today 11:1034–1040. doi:10.1016/j.drudis.2006.09.004 PubMedView ArticleGoogle Scholar
- Hwang YS, Tsai WC, Lu YH, Lin CC, Chen YF (2004) Effect of atorvastatin on the expression of CD40 ligand and P-selectin on platelets in patients with hypercholesterolemia. Am J Cardiol 94:364–366. doi:10.1016/j.amjcard.2004.04.037 PubMedView ArticleGoogle Scholar
- Kuypers FA, Larkin SK, Emeis JJ, Allison AC (2007) Interaction of an annexin V homodimer (Diannexin) with phosphatidylserine on cell surfaces and consequent antithrombotic activity. Thromb Haemost 97:478–486PubMedGoogle Scholar
- Hale SL, Allison AC, Kloner RA (2011) Diannexin reduces no-reflow after reperfusion in rabbits with large ischemic myocardial risk zones. Cardiovasc Ther 29:e42–e52. doi:10.1111/j.1755-5922.2010.00223.x PubMedView ArticleGoogle Scholar
- Molski M, Groth A, Allison AC, Hendrickson M, Siemionow M (2009) Diannexin treatment decreases ischemia-reperfusion injury at the endothelial cell level of the microvascular bed in muscle flaps. Ann Plast Surg 63:564–571. doi:10.1097/SAP.0b013e3181935a4e PubMedView ArticleGoogle Scholar
- Wever KE, Wagener FA, Frielink C, Boerman OC, Scheffer GJ, Allison A et al (2011) Diannexin protects against renal ischemia reperfusion injury and targets phosphatidylserines in ischemic tissue. PLoS ONE 6:e24276. doi:10.1371/journal.pone.0024276 PubMedPubMed CentralView ArticleGoogle Scholar
- Shen XD, Ke B, Zhai Y, Tsuchihashi SI, Gao F, Duarte S et al (2007) Diannexin, a novel annexin V homodimer, protects rat liver transplants against cold ischemia-reperfusion injury. Am J Transplant 7:2463–2471PubMedView ArticleGoogle Scholar
- Hashimoto K, Kim H, Oishi H, Chen M, Iskender I, Sakamoto J et al (2016) Annexin V homodimer protects against ischemia reperfusion-induced acute lung injury in lung transplantation. J Thorac Cardiovasc Surg 151:861–868. doi:10.1016/j.jtcvs.2015.10.112 PubMedView ArticleGoogle Scholar