FKBP51 increases the tumour-promoter potential of TGF-beta
© Romano et al.; licensee Springer. 2014
Received: 4 November 2013
Accepted: 26 December 2013
Published: 27 January 2014
FKBP51 (FKBP5 Official Symbol) is a large molecular weight component of the family of FK506 binding proteins (FKBP). In recent years, research studies from our laboratory highlighted functions for FKBP51 in the control of apoptosis and melanoma progression. FKBP51 expression correlated with the invasiveness and aggressiveness of melanoma. Since a role for TGF-β in the enhanced tumorigenic potential of melanoma cells is widely described, we hypothesized a cooperative effect between FKBP51 and TGF-β in melanoma progression.
SAN and A375 melanoma cell lines were utilized for this study. Balb/c IL2γ NOD SCID served to assess the ability to colonize organs and metastasize of different cell lines, which was evaluated by in vivo imaging. Realtime PCR and western blot served for measurement of mRNA and protein expression, respectively.
By comparing the metastatic potential of two melanoma cell lines, namely A375 and SAN, we confirmed that an increased capability to colonize murine organs was associated with increased levels of FKBP51. A375 melanoma cell line expressed FKBP51 mRNA levels 30-fold higher in comparison to the SAN mRNA level and appeared more aggressive than SAN melanoma cell line in an experimental metastasis model. In addition, A375 expressed, more abundantly than SAN, the TGF-β and the pro angiogenic TGF-β receptor type III (TβRIII) factors. FKBP51 silencing produced a reduction of TGF-β and TβRIII gene expression in A375 cell line, in accordance with previous studies. We found that the inducing effect of TGF-β on Sparc and Vimentin expression was impaired in condition of FKBP51 depletion, suggesting that FKBP51 is an important cofactor in the TGF-β signal. Such a hypothesis was supported by co immunoprecipitation assays, showing that FKBP51 interacted with either Smad2,3 and p300. In normal melanocytes, FKBP51 potentiated the effect of TGF-β on N-cadherin expression and conferred a mesenchymal-like morphology to such round-shaped cells.
Overall, our findings show that FKBP51 enhances some pro oncogenic functions of TGF-β, suggesting that FKBP51-overexpression may help melanoma to take advantage of the tumor promoting activities of the cytokine.
KeywordsMelanoma TGF-β FKBP51 Metastasis
FK506 binding protein 51 (FKBP51)  is an immunophilin physiologically expressed in lymphocytes and several other tissues . FKBP51 structure includes C-terminal TPR domains, responsible for protein protein interactions with heat shock proteins HSP90 and HSP70, and N-terminal domains with peptidyl-prolyl isomerase activity . Due to its multifunctional domains, FKBP51 regulates several biological processes in the cell, through protein-protein interaction . Very recently, we found an aberrant expression of this protein in melanoma [3, 4]. We demonstrated that FKBP51 promotes activation of epithelial-to-mesenchymal transition (EMT) genes and improves melanoma cell migration and invasion . Consistent with this finding, FKBP51-targeting prevented melanoma colonization of liver and lungs in a mouse model of experimental metastasis . The pleiotropic cytokine TGF-β plays a relevant role in EMT . Notably, TGF-β acts as an early tumor suppressor, but functions later as a tumour promoter and a pro-metastatic agent . In normal melanocytes, TGF-β acts as a potent inhibitor of proliferation and differentiation [7, 8]; in advanced melanoma, TGF-β favors cell proliferation and dissemination, peri-tumoral angiogenesis, EMT and tumor escape from immune surveillance [9–11]. The mechanism underlying evasion from a cytostatic response to TGF-β in tumor cells remains somewhat elusive. Our previous results showed that FKBP51 positively regulates the expression of TGF-β, in melanoma . We hypothesized a role for FKBP51 in potentiating the tumour promoting activities of TGF-β, in melanoma.
Cell culture and transfection and reagents
The melanoma cell lines SAN and A375 were cultured as described . For siRNA transfection, 24 hours before transfection, cells were seeded into six-well plates at a concentration of 2×105 cells/ml to obtain 30–60% confluence at the time of transfection. Then, cells were transfected with specific short-interfering oligoribonucleotide (siRNA) or with a non silencing oligoribonucleotide (NS RNA) as control, at a final concentration of 50 nM using Metafectene according to the manufacturers’ recommendations. NS RNA (AllStars neg control siRNA) and siRNA for FKBP51 (5′-ACCUAAUGCUGAGCUUAUA-3) were purchased from Qiagen (Germantown, Philadelphia, USA). ShRNA transfection was performed using the Expression ArrestTM shRNA system (Open Biosystem, AL, USA). Expression ArrestTM shRNAs are cloned into the incompetent replication pSHAG-MAGIC2 (pSM2) retroviral vector. This vector has a Murine Stem Cell Virus (MSCV) backbone combined with packaging extract for mammalian cell infection, a PGK- Puro selection for transfection stability in mammalian cells and a chloramphenicol/kanamycin bacterial selection marker. The stable transfectants were obtained after a 1 month selection of positive clones. The selection was performed by adding puromycin (Sigma Aldrich, Saint Louis, Missouri, USA) to cell culture medium every 48 hours. For a first stronger selection puromycin was used at a dose of 800 ng/ml; after a week it was used a dose of 200 ng/ml to complete and maintain the selection. To create FKBP51 over expressing SAN melanoma cells, a p3XFLAG-CMV™-14 expression vector (Sigma Aldrich, S. Louis, Missouri, USA) carrying the FKBP51 gene was transfected using Metafectene (Biontex, Munich, Germany), according to manufacturer’s recommendations. A void p3×Flag-CMV vector was also transfected to generate control cells. To generate stable populations, cells were selected using 500 ug/ml G418 (GIBCO, Invitrogen, Carlsbad, CA) at 24 h post-transfection and grown until colony formation. TGF-β (Sigma Aldrich) was used at the dose of 10 ng/ml.
After the approval of the local institutional animal research committee, animal studies were performed following detailed internal regulations devised according to the U.S. Public Health Service Policy on Humane Care and Use of Laboratory Animals, available from the Office of Laboratory Animal Welfare, National Institutes of Health, Department of Health and Human Services, RKLI, Suite 360, MSC 7982, 6705 Rockledge Drive, Bethesda, MD 20892–7982 and the United Kingdom Coordinating Committee on Cancer Prevention Research's Guidelines for the Welfare of Animals in Experimental Neoplasia (published online 25 May 2010). Melanoma cells (1.5×106 SAN or A375 in 100 μl PBS) were injected systemically into the lateral tail vein of 4- to 6-week-old Balb/c IL2γ NOD SCID (null) mice (Charles River Laboratory, Wilmington, MA). After 3 weeks, imaging was performed using a dedicated animal PET/CT scanner (eXplore Vista, GE Healthcare). A dose of 8.3 mCi/kg (307.1 MBq/kg) of F-FDG was administrated in a bolus in a total volume of 100 μl. Animals were maintained at a temperature of 23°C during the biodistribution of F-FDG. After 45 minutes, mice were anesthetized with ketamine 50 mg/kg and xylazine 40 mg/kg and symmetrically positioned on a warm bed with micropore tape. Then, a 20-min static PET (two bed position with a 4.8-cm axial field-of-view; energy window 250–700 keV) scan was performed. PET images were processed using a 2D-OSEM iterative algorithm (voxel size of 0.3875 × 0.3875 × 0.7750 mm3) including random scatter correction, dead time, decay, and attenuation correction using CT data (eXplore Vista Software).
Western blot and immunoprecipitation
Whole cell lysates were homogenized in modified RIPA  buffer as described and assayed in Western blot as described . Primary antibodies against FKBP51 (F-13; goat polyclonal; Santa Cruz Biotechnology, CA, USA); Smad 2/3 (H465, rabbit polyclonal; Santa Cruz Biotechnology); SPARC (H-90, rabbit polyclonal; Santa Cruz Biotechnology); N-Cadherin (5D5, mouse monoclonal; Abcam, Cambridge, UK); G3PDH (D16H11, rabbit monoclonal; Cell Signaling, Danvers, USA); were used diluted. 1:500. For immunoprecipitation (IP), 500 ug of total lysate was precleared for 1 hour. Three μg anti-KAT3B/p300 (Novus Biologicals, Littleton, CO, USA) or anti-FKBP51 (H100, rabbit polyclonal, Santa Cruz Biotechnology), was added to total lysate, kept in rotation, at 4°C over night. After, 25 uL protein A Agarose (Santa Cruz Biotechnology) was added to the mixture and precipitation took place for 4 h, with rotation at 4°C. Samples were then washed in RIPA and separated by 10% SDS-PAGE. Anti-KAT3B/p300 (Novus Biologicals), anti-FKBP51 (mouse polyclonal; Abnova, Taipei, Taiwan) were used for detection of pulled down proteins.
Total RNA was isolated from cells using Trizol (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instructions. One microgram of each RNA was used for cDNA synthesis with Moloney Murine Leukemia Virus Reverse Transcriptase (M-MLV RT, Invitrogen, Carlsbad, CA, USA). Gene expression was quantified by Real-time PCR using iQ™SYBR®Green Supermix (Biorad, CA, USA) and specific Real-time validated QuantiTect primers for FKBP51 (QT00056714: NM_001145775 800 e 900 bp; NM_001145776 650 and 750 bp; NM_001145777 650 and 750 bp; NM_004117 600 and 700 bp); TGF-β (QT00000728: NM_000660 1200 and 1300 bp), TβRIII (QT00013335: NM_000118 600 and 750 bp; NM_001114753 600 and 750 bp), N-cadherin (QT00063196: NM_001792 2800 and 2900 bp) (Qiagen, Germantown, Philadelphia, USA), cyclin B (QT00006615: NM_031966 1250 and 1350 bp), vimentin (QT00095795: NM_003380 900 e 1000 bp), slug (QT00044128: NM_003068200 e 350 bp). Relative quantitation of the transcript was performed using co-amplified ribosomal 18S as an internal control for normalization. Ribosomal 18S primers Fw 5′-CGATGCGGCGGCGTTATTC-3′ and 18S Rev 5′-TCTGTCAATCCTGTCCGTGTCC-3′.
Vimentin expression was measured in flow cytometry. Briefly, after centrifugation for 5 min at 400× g, 1×105 cells were fixed with 2% paraformaldehyde in Tris Buffered Saline solution (TBS) for 20 min and permeabilized with 0.1%TRITON-X-100 and 0.1% Sodium Citrate in TBS for 3 min in ice. Cells were, then, incubated with the mouse monoclonal antibody anti-Vimentin, IgG1 clone-V9; 1:100 (Novocastra™, Milan, Italy) or a control IgG, for 30 min at 4°C. After incubation, cells were washed and stained with a secondary FITC-conjugated anti-mouse antibody and analyzed in flow cytometry.
Primary melanocyte cultures
Human melanocytes were isolated from an acquired melanocytic naevus, surgically excised, which was obtained after informed consent of the subject, and grown in Melanocyte Medium BulletKitTM - 500 ml CloneticsTM MGMTM-4 BulletKitTM (CC-3249) containing the following growth supplements: CaCl2, 1.0 ml; BPE, 2.0 ml; rhFGF-B, 1.0 ml; rh-Insulin, 1.0 ml; Hydrocortisone, 0.5 ml; PMA, 0.5 ml; GA-1000, 0.5 ml; FBS, 2.5 ml (Gibco, Grand Islands, NY, USA). Briefly, the naevus was placed in sterile phosphate buffered saline (PBS) solution. Subcutaneous fat and deep dermis were excised from the sample, and the remaining tissue was cut into smaller pieces, followed by trypsinization (0.25% trypsin, Gibco) at 37°C for 30 min. Trypsin activity was neutralized with FBS. Each piece was placed under a sterile glass in order to press the tissue and favor cells leaking. Cells isolated from melanocytic naevus started to growth out of the tissue pieces after a couple of weeks. Thenafter, tissues were eliminated and contaminating fibroblasts were selectively killed by treating the cultures with 100 μg/ml G418 for 3–4 days. Melanocytes were subsequently isolated from keratinocytes by gentle trypsinization and passed at a ratio of 1:3 once every 7–14 days. After 1 month, melanocytes were transfected with a p3XFLAG-CMV™-14 expression vector (Sigma Aldrich, S. Louis, Missouri, USA) carrying the FKBP51 gene, or a void vector as control, Metafectene (Biontex, Munich, Germany). After a 3day culture, 25 ng/ml TGF-β for further 3 days; then a picture from different melanocyte cultures was captured and cells were harvested and processed for Real time-PCR assay.
Results and discussion
The enhanced tumorigenic potential of melanoma cells is accompanied by increased levels of FKBP51 and TGF-β
FKBP51 positively regulates the TGF-β signal in melanoma
FKBP51 upregulates EMT features in TGF-β-cultured normal skin melanocytes
In melanoma, several models of resistance to TGF-β growth suppressor signals have been suggested, also in view of the dysregulation of fundamental cellular effectors and signaling pathways [9, 22]. We propose FKBP51 may represent an element, within melanoma cell context, that allows the tumour to take advantage of tumour-promoting activities of the TGF-β. Our findings suggested that FKBP51 increases melanoma sensitivity to TGF-β, and, particularly, the tumour promoting activities of the cytokine, possibly mediated by a mechanism involving recruitment of Smad to p300 coactivator. The differential expression of FKBP51 in normal melanocytes, in which the immunophilin is hardly detectable , and melanoma, in which the protein is overexpressed, might in part account for differential functions exerted by TGF-β in normal and malignant melanocytes. In addition, the concept that FKBP51 expression increases with melanoma progression, is also in accordance with the notion that TGF-β acts as an early tumor suppressor and late tumour promoter [5, 6, 14].
FK506 binding protein 51
Transforming growth factor-β
TGF-β receptor type III
TGF-β receptor type I
Epithelial to mesenchymal transition
- NS RNA:
Non silencing RNA
Work was supported by Italian Association for Cancer Research (AIRC, project 10452), and the Cardiovascular Service SRL.
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