The antitumor immune response is a critical defense system that eliminates malignant cells. The failure of the system results in immune escape and proceeds to tumor growth. We have previously showed that estrogen receptor-binding fragment-associated antigen 9 (EBAG9) is a relevant cancer biomarker and facilities immune escape of cancers from the immune surveillance. EBAG9 in cancer cells suppresses T-cell infiltration into tumor in vivo, whereas that in host immune cells functions as a limiter for T-cell cytotoxicity. Considering that EBAG9 plays immune suppressive roles in both tumor and microenvironment, we here questioned whether EBAG9 is a transferable protein from cancer to surrounding T cells and affects antitumor immune response. In this study, we showed that spontaneous development of prostate cancer was repressed in a model of Ebag9 knockout mice crossed with transgenic adenocarcinoma of the mouse prostate (TRAMP) mice. We identified TM9SF1 as a collaborative EBAG9 interactor, which regulates epithelial-mesenchymal transition (EMT) in cancer cells. Notably, extracellular vesicles (EVs) from EBAG9-overexpressing prostate cancer cells have a potential to facilitate immune escape of tumors by inhibiting T-cell cytotoxicity and modulating immune-related gene expression in T cells. Furthermore, we showed that a neutralizing antibody for EBAG9 could rescue the EV-mediated immune suppression by recovering T-cell cytotoxicity. In addition to its autocrine functions in cancer cells, EBAG9 could behave as a new class of immune checkpoint that suppresses tumor immunity in a secretory manner. We propose that EBAG9-targeting cancer treatment could be alternative therapeutic options for advanced diseases, particularly for those with EBAG9 overexpression.
Cancer progression is regulated by interactions between cancer cells and their tissue microenvironment containing immune cells. Malignant cells are eliminated by immune surveillance at first; however, cancer cells will often obtain ability to evade from the immune system, a process known as immune escape1. T lymphocytes are primary mediators of the adaptive immune response and play an important role in the tumor surveillance2,3. In particular, cytotoxic CD8+ T lymphocytes (CTLs) are activated to kill cancer cells through the recognition of specific antigen on the cancer cells by using T-cell receptor (TCR) system. Understanding the mechanisms of tumor immunity are clinically relevant to develop alternative immune therapies4.
Estrogen receptor-binding fragment-associated antigen 9 (EBAG9) has been originally identified as an estrogen-responsive gene in breast cancer cells5. EBAG9 stimulates the migration of cultured cancer cells and clinically associates with pathophysiology of various cancers including breast, ovarian, prostate, hepatocellular, renal, and bladder cancers6,7,8,9,10,11,12. We previously showed that EBAG9 immunoreactivity was inversely associated with the infiltration of CD3+ T cells in breast cancer specimens6. In Renca syngeneic transplantation renal cancer models, we demonstrated that EBAG9 overexpression stimulated the tumor formation of syngeneic transplantation model10. These findings implied that EBAG9 functions as a tumor-promoting factor through influencing host tissue microenvironment, including immune cells; however, the precise mechanism of cancer-derived EBAG9 remains elusive.
Notably, we recently showed that tumor formation and metastasis of transplanted cancer cells were repressed in Ebag9 knockout (Ebag9KO) mouse host, and CD8+ T cells infiltration was significantly enhanced in the transplanted tumors13. The tumor-infiltrated CD8+ T cells from Ebag9KO host exhibited increased degranulation and cytotoxic activity. Moreover, adoptive transfer of transplanted tumor-infiltrated Ebag9KO CD8+ T cells suppressed inoculated tumor growth in wild-type host. In the model, the cytotoxic activity of Ebag9KO CD8+ T cells was enhanced as the T cell-derived granzymes were upregulated without increased proliferation of T cells14. EBAG9 was also shown to interact with γ2-adaptin, a clathrin adaptor-related protein, which might be involved in endosome-to-lysosome maturation15. These findings suggested that host EBAG9 functions as a suppressor for tumor growth and metastasis in tumor microenvironment by repressing the cytotoxicity of immune cells.
Recent advance in cancer research revealed that tumor cells often secret larger amounts of extracellular vesicles (EVs), including exosomes than normal cells into their microenvironment16,17. Exosomes are defined as a subset of small extracellular vesicles (30–100 nm diameter) and contain various bioactive molecules including nucleic acids and proteins18,19. As exosomes primarily function as mediators in intercellular communication and molecular transfer, a role of exosomes in tumor development and metastasis has attracted considerable attention20. In particular, it is notable that tumor-derived exosomes sometimes facilitate immunosuppression by inhibiting the activities of immune cells21.
Here we questioned whether EBAG9 or cancer-derived EVs containing EBAG9 affect cancer cell biology, as well as immune surveillance system in tumor microenvironment. In the study of antitumor immune response, we used a model of autochthonous spontaneous transgenic adenocarcinoma of the mouse prostate (TRAMP)22. When TRAMP mice were crossed with Ebag9KO mice, we showed that prostate tumor development was repressed compared with parental TRAMP mice. We identified a novel interacting factor for EBAG9, transmembrane 9 superfamily member 1 (TM9SF1)23,24. TM9SF1 and EBAG9 cooperatively regulate prostate cancer cell migration by modulating the expression of genes involved in epithelial-mesenchymal transition (EMT). Notably, we showed that cancer-derived EVs contain EBAG9 protein, which promotes EMT of prostate cancer cells, as well as represses the cytotoxicity of T cells. EBAG9 monoclonal antibody substantially neutralizes the EV-dependent reduction of T cell-mediated cytotoxicity. We infer that tumor-derived EV-mediated EBAG9 protein is a critical factor that potentially facilitates tumor progression by negatively modulating immune cells in microenvironment.
Cancer development is reduced in spontaneous prostate cancer model mice with EBAG9 deficiency
To assess the physiological function of EBAG9 in host defense against prostate cancer development, we used a model of Ebag9 knockout (Ebag9KO) mice13 crossed with TRAMP mice (C57BL/6-Tg(TRAMP)8247Ng/J obtained from Jackson Lab), which are characterized to develop spontaneously transgenic adenocarcinoma of the mouse prostate22. TRAMP transgene hemizygous mice harbor aggressive forms of prostate cancer with distant metastasis due to the expression of probasin-driven SV40 T antigen. Whole weights of genitourinary tract organs, including prostate are often used as an indicator for monitoring tumor progression22. As a control strain for Ebag9KO;TRAMP(+) mice, we also generated Ebag9WT;TRAMP(+) mice. Ebag9KO;TRAMP(+) male mice showed decreased genitourinary weight compared with Ebag9WT;TRAMP(+) mice at 1 year after birth (Fig. 1a, b). To evaluate infiltrating T cells in the whole tumor, qRT-PCR was performed using RNAs prepared from the generated tumors25,26,27. It was notable that the mRNA expression of Cd8, a selective marker for cytotoxic T cells, was significantly increased in prostate cancer tissues derived from Ebag9KO;TRAMP(+) mice compared with control mice (Fig. 1c). These results suggest that host EBAG9 could facilitate cancer development by inhibiting CD8+ T-cell infiltration.
EBAG9 expression in cancer cells promotes cell migration by affecting EMT-related gene levels
To investigate the role of EBAG9 in the pathophysiology of prostate cancer cells, we performed functional studies using siRNA targeting EBAG9 (siEBAG9) in androgen-sensitive LNCaP and androgen-refractory DU145 cells. Western blot analysis showed that siEBAG9 substantially suppressed EBAG9 protein expression in LNCaP cells (Fig. 2a). siEBAG9 significantly inhibited the migration of LNCaP cells (Fig. 2b and Supplementary Figure S1A) and DU145 cells (Supplementary Figure S2A). Decrease of EBAG9 mRNA in DU145 cells treated with siEBAG9 was confirmed by qRT-PCR (Supplementary Figure S2B). We examined the expression of epithelial-mesenchymal transition (EMT)-associated genes as cancer cell migration is often associated with EMT28. siEBAG9 decreased the expression levels of a mesenchymal marker, VIM mRNA and protein, and an EMT-related transcription factor, SNAI2 mRNA, in LNCaP cells (Fig. 2c and Supplementary Figures S1B and C). From the viewpoint of EBAG9 overexpression, LNCaP cells stably expressing EBAG9 (LNCaP-EBAG9) exhibited the increases of migration (Fig. 3a) compared with control cells transfected with empty vector (LNCaP-Vector). In addition, VIM at mRNA and protein levels and SNAI2 at mRNA level, were upregulated in LNCaP-EBAG9 cells (Fig. 3b and Supplementary Figure S3). The gain- and loss-of-function studies of EBAG9 indicate that EBAG9 could modulate the gene expression associated with EMT, which may contribute to prostate cancer progression.
TM9SF1 interacts with EBAG9 and regulates EMT in prostate cancer cells
To clarify the molecular mechanism of EBAG9, we explored its interacting partners by yeast two-hybrid screening and identified several candidate proteins that are associated with cellular functions of molecular chaperone, fatty acid metabolism, ubiquitin modification, and protein secretion. We focused on transmembrane 9 superfamily member 1 (TM9SF1), whose protein co-localizes with lysosomes in cytosol and plays a role in autophagy23. We examined whether EBAG9 physically associates with TM9SF1. 293T cells were cotransfected with HA-TM9SF1 and Flag-EBAG9. Immunoprecipitation was carried out using antibodies to EBAG9 or TM9SF1, and immunoblots of the immunoprecipitates were further detected with anti-EBAG9 and anti-TM9SF1 antibodies. As shown in Fig. 4a, EBAG9 interacted with TM9SF1. Cytosolic co-localization of EBAG9 and TM9SF1 proteins was observed fluoromicroscopically in HeLa cells transfected with GFP-TM9SF1 and DsRed-EBAG9 (Fig. 4b). To investigate the role of TM9SF1 in prostate cancer cells, we performed functional studies using siRNA targeting TM9SF1 (siTM9SF1) in LNCaP cells. siTM9SF1 significantly inhibited the migration of LNCaP cells (Fig. 4c and Supplementary Figure S4A). siTM9SF1 also downregulated VIM and SNAI2 expressions in LNCaP cells (Fig. 4d and Supplementary Figure S4B). We further analyzed whether TM9SF1 contributes to EBAG9-dependent increase in cell migration. siTM9SF1 partially impaired the increases in cell migration (Fig. 4e) and SNAI2 expression (Fig. 4f) in EBAG9-overexpressing LNCaP cells. These results suggest that TM9SF1 could cooperatively function with EBAG9 to regulate cell migration and EMT in prostate cancer cells.
EVs from EBAG9-overexpressing LNCaP cells stimulate parental cell migration
Cancer cells are known to secrete various factors which will affect their behavior and tumor microenvironment in autocrine or paracrine manner29,30. We questioned whether EBAG9 protein is secreted in EVs to influence cancer microenvironment. Western blot analysis detected endogenous expression of EBAG9 protein in the EVs prepared from conditioned media of LNCaP-Vector and LNCaP-EBAG9 cells (Fig. 5a, lower signals), indicating that EBAG9 is primarily secreted from prostate cancer cells. Exogenously introduced Flag-EBAG9 was detected only in LNCaP-EBAG9 cells (Fig. 5a, upper signals). To investigate EV internalization, LNCaP-EBAG9 cell-derived EVs were labeled with green fluorescent PKH67 and then added into the culture media of parental LNCaP cells (Fig. 5b). PKH67 signal was accumulated in parental cells, indicating that EVs could be transferred into LNCaP cells in autocrine/paracrine manners. Moreover, LNCaP-EBAG9 cell-derived EVs increased the migration of parental cells (Fig. 5c) and DU145 cells (Supplementary Figure S2C) compared with control cell-derived EVs.
Cancer-derived EBAG9-containing EVs inhibit cytotoxic activity and modulate immune-related gene expression in T cells
We next investigated whether LNCaP-EBAG9 cell-derived EVs affect T cell function. PKH67-labeled EVs from LNCaP-EBAG9 cells were accumulated in T-leukemia MOLT4 cells 8 and 24 h after co-culture treatment (Fig. 6a). Lactate dehydrogenase (LDH) cytotoxicity assay was also performed to evaluate the effects of EBAG9-containing EVs to cytotoxic activity of MOLT4 cells. LNCaP-EBAG9 cell-derived EVs significantly decreased the cytotoxicity of MOLT4 cells against LNCaP cells compared with control cell-derived EVs (Fig. 6b). Interestingly, pretreatment of LNCaP-EBAG9 cell-derived EVs with EBAG9 monoclonal antibody recovered the cytotoxicity of MOLT4 cells to the level equivalent to pretreatment with control IgG, indicating that the antibody could neutralize T cell cytotoxicity. In addition, LNCaP-EBAG9 cell-derived EVs downregulated the expression of immune-related genes containing interferon gamma (IFNG), interleukin 10 receptor (IL10R), granzyme B (GZMB), and chemokine (C-X-C motif) receptor 3 (CXCR3) in MOLT4 cells (Fig. 6c). Taken together, we infer that cancer-derived EBAG9-containig EVs affect both on cancer cells and infiltrated T cells by promoting tumor cell migration and suppressing T cell cytotoxicity, respectively (Fig. 6d). We propose that the EBAG9 interactor TM9SF1 may cooperatively function in the EBAG9-mediated tumor-promoting effects.
In this study, Ebag9KO mice crossed with TRAMP mice demonstrated that EBAG9 plays a crucial role in prostate cancer development. In prostate cancer cells, EBAG9 regulated cell migration and EMT-related gene expression through the interaction with TM9SF1. In addition, EVs, which contained overexpressed EBAG9 protein, increased the migration of prostate cancer cells. Intriguingly, EBAG9-overexpressing EVs inhibited the cytotoxic activity and immune-related genes expression in MOLT4 cells. These results suggested that cancer-derived EBAG9 would contribute to tumor progression in autocrine and/or paracrine fashions interacting with its novel partner TM9SF1. EBAG9 would transfer to immune T cells through EVs and negatively regulate tumor surveillance in host cells. Another possibility which has not been entirely rules out is that EBAG9 functions through the membrane surface in the recipient cell.
TM9SF1 is a member of the transmembrane 9 superfamily, whose precise function remains unknown. TM9SF1 has been identified by screening genes stimulating autophagosome formation in mammalian cells23. TM9SF1 protein is shown to co-localize to lysosomes with LC3, microtubule-associated protein 1A/1B-light chain 3, which is known to form a stable association with the membrane of autophagosomes23. TM9SF1 overexpression increases autophagosome formation and actually induces autophagy23. It is also shown that TM9SF1 protein is involved in late endosomes and lysosomes31. Although TM9SF1 is ubiquitously expressed in various normal tissues, TM9SF1 overexpression is reported in several cancers. In breast cancer, TM9SF1 has been identified by screening cancer specific antigens that are potentially applied to immunotherapy32. The screening was specialized for exploring genes encoding functional transmembrane motifs that are differentially expressed between cancer and normal cells. In this study, TM9SF1 was overexpressed in breast cancer tissues compared with normal breast. In urinary bladder cancer, expression microarray analysis revealed that TM9SF1 is one of the genes commonly overexpressed in cancer tissues compared to normal tissues24. While the mechanism of TM9SF1 remains to be elusive, we speculate that EBAG9 and TM9SF1 could cooperatively regulate cancer cell migration.
EMT often associates with enhanced cell migration and metastasis, resulting in aggressive cancer phenotypes33. Upregulation of vimentin (VIM) expression is a typical characteristic of cells undergoing EMT. Several transcription factors, such as SNAIL (SNAI1) and SLUG (SNAI2), are also known to play crucial roles in EMT34. For example, SNAI2 functions as a metastasis regulator in tumors and its expression is associated with poor clinical outcomes for patients with several types of cancer35. This study revealed that EBAG9 modulates the expression of EMT-related genes containing VIM, SNAI1, and SNAI2 in prostate cancer cells, suggesting that EBAG9 could stimulate cancer progression and invasion through EMT pathway.
It has been reported that EBAG9 is localized in the Golgi apparatus and increases the generation of the tumor-associated O-linked glycan Tn (N-acetyl-D-galactosamine, GalNAc) and the closely related TF (Thomsen-Friedenreich, Galβ1–3GalNAc) antigens36. EBAG9 protein was also shown to localize in the coat protein complex I (COPI)-coated transport vesicles, and EBAG9 negatively regulates the COPI-dependent endoplasmic reticulum-to-Golgi transport pathway and exocytosis37. Taken together, EBAG9 would contribute to pathogenesis of cancer cells by inhibiting intracellular membrane trafficking, which results in the alteration of glycosylation modification of cellular proteins, including tumor-associated glyco-antigens38. We could speculate that the EBAG9-mediated glycosylation may modify unknown EMT-related proteins in cancer cells. In line with this speculation, atypical glycans undergoing EMT have been identified in cancer cells39.
This study showed that cancer-derived EVs contain EBAG9 protein, and proposed that EV-mediated EBAG9 transfer would contribute to cancer cell migration and immune escape. Several studies have reported that tumor-derived EVs can induce T-cell apoptosis40,41. For instance, EVs expressing Fas ligand increase T-cell apoptosis in human melanoma and colorectal cancer cells42,43. EVs isolated from various cancer cell lines also downregulate natural-killer group 2, member D (NKG2D) expression in NK cells and CD8+ cytotoxic MOLT4 cells44, where NKG2D is known to function as an activating receptor on the cell surface. In addition, tumor cell-derived EVs modulate inflammatory tumor microenvironment where NF-kappaB signaling plays a critical role45,46. We demonstrated that EBAG9 protein is secreted in cancer-derived EVs, which are transferred to cancer cells and T cells, and function as a suppressor for T cell cytotoxicity. The present study provides new insights into tumor progression and anti-tumor immunity, and will provide a potential therapeutic target for advanced cancers.
Materials and methods
LNCaP, DU145, 293T, MOLT4, and HeLa cell lines were obtained from the American Type Culture Collection. LNCaP and MOLT4 cells were cultured in RPMI, supplemented with 10% fetal bovine serum (FBS), penicillin (50 U/ml), and streptomycin (50 μg/ml). DU145, 293T, and HeLa cells were cultured in DMEM, supplemented with 10% FBS, penicillin (50 U/ml), and streptomycin (50 μg/ml). LNCaP cells stably expressing flag-tagged EBAG9 (EBAG9 #4 and #6) and control vector (Vector #3 and #5) were selected by G418. Cells were cultured in a humidified atmosphere containing 5% CO2 at 37 °C. Short tandem repeat (STR) analyses were performed for the authentication of the cell lines, which were not contaminated with mycoplasma based on the examination by MycoAlert mycoplasma detection kit (Lonza, Walkersville, MD, USA).
C57BL/6 TRAMP mice (C57BL/6-Tg(TRAMP)8247Ng/J) were purchased from the Jackson Laboratory and Ebag9KO mice (Ebag9−/−) were described previously13. TRAMP mice were crossed with Ebag9KO mice to generate Ebag9KO;TRAMP(+) mice. At 1 year old, mice were killed and the genitourinary (GU) complex (consisting of prostate, seminal vesicles, urethra, and empty bladder) was weighed. Mice were kept under specific pathogen-free conditions and fed dry food and water ad libitum. The results are shown as mean values ± SD (Ebag9KO;TRAMP(+); n = 10, Ebag9WT;TRAMP(+); n = 17). Statistical analysis was carried out using the modified Thompson tau technique and two-sided Student’s t-test. *P < 0.05. All experiments were performed according to the guidelines for the care and use of laboratory animals of Saitama Medical University. Animals were randomly assigned to the groups and the experiments were performed without blinding. The sample size estimate was based on our pilot study.
Small interfering RNA
Small interfering RNAs (siRNAs) of EBAG9 (siEBAG9 #1 and #2) and TM9SF1 (siTM9SF1 #1 and #2) were synthesized by RNAi Inc. (Tokyo, Japan) using an algorithm that significantly improves the target specificity of siRNA, in particular, by efficiently estimating off-target sequences47. The specific sequences targeting EBAG9 and TM9SF1 were as follows: siEBAG9 #1 sense 5′-CUCAUUCCUAAAGAGAUUAAU-3′ and antisense 5′-UAAUCUCUUUAGGAAUGAGAA-3′; siEBAG9 #2 sense 5′-AAGAAGAUGCAGCCUGGCAAG-3′ and antisense 5′-UGCCAGGCUGCAUCUUCUUCU-3′; siTM9SF1 #1 sense 5′-GAAUGGCUGAGUCUUUGUAUG-3′ and antisense 5′-UACAAAGACUCAGCCAUUCGG-3′; siTM9SF1 #2 sense 5′-GCCCUGAGAAGAUACGUCACA-3′ and antisense 5′-UGACGUAUCUUCUCAGGGCAG-3′. A non-targeting control siRNA (siControl) with no homology to known gene targets in mammalian cells were also obtained from RNAi Inc.47. Transfection of siRNA was carried out using RNAiMAX transfection reagent (Life Technologies, Carlsbad, CA, USA).
Cell migration was examined by using cell culture inserts with 8.0-μm pore size PET filters (Becton Dickinson Labware, Bedford, MA, USA). Cells were seeded into the culture dish and transfected with 10 nM siEBAG9 #1, siEBAG9 #2, siTM9SF1 #1, siTM9SF1 #2 or siControl using Lipofectamine RNAiMAX reagent (Life Technologies). After transfection, 5 × 104 LNCaP or 3 × 104 DU145 cells were suspended in the culture medium and added to the upper chamber. For stable cell lines (EBAG9 #4 and #6, and Vector #3 and #5), 5 × 104 cells were added to the upper chamber. Cells were then incubated for 24 or 48 h at 37 °C. The cells on the lower surface of the filter were fixed in methanol and stained with Giemsa’s staining solution. After washing, the cells on the lower surface were counted in at least 5 fields under the microscope. The results were shown as mean ± SD (n = 5). Statistical analysis was carried out using two-sided Student’s t-test. *P < 0.05; **P < 0.01.
Yeast two-hybrid screen
Saccharomyces cerevisiae strain EGY48 was transformed with pEG202-NLS-human EBAG9, and further transformed with a mouse embryo cDNA library (OriGene, Rockville, MD, USA). Screening was carried out according to the manufacturer’s protocol. Positive colonies were selected through growth on agar plates lacking leucine, and verified by galactose-dependent lacZ expression. Plasmids were recovered from the several positive clones and sequenced using the dideoxy termination method.
The cDNA coding for TM9SF1 was subcloned into pEGFP-N1 expression vector (Clontech, Palo Alto, CA, USA) using XhoI and HindIII restriction sites. The TM9SF1 cDNA was N-terminally tagged with the HA epitope and subcloned into the pcDNA3 vector (Invitrogen, Carlsbad, CA, USA) using BamHI and XhoI restriction sites. The cDNA coding for EBAG9 was subcloned into pDsRed-N1 vector (Clontech) using XhoI and HindIII restriction sites. The EBAG9 cDNA was N-terminally tagged with the Flag epitope and subcloned into the pcDNA3 vector using EcoRI and XhoI restriction sites. Transfection of plasmids was carried out using Lipofectamine 2000 transfection reagent (Life Technologies).
Western blot analysis and immunoprecipitation
The expression vectors for EBAG9 and TM9SF1 were introduced into 293T cells by transfection for 48 h. Cells were suspended in lysis buffer (20 mM HEPES, pH 7.9, 300 mM NaCl, 1 mM EDTA, 15% glycerol, 0.5% Nonidet P-40, 1 mM Na3VO4, 1 mM phenylmethylsulfonyl fluoride), rocked gently for 50 min at 4 °C, and centrifuged at 14,000×g for 5 min at 4 °C. The supernatants were used as cell lysates. Cell lysates were resolved by SDS-PAGE and electrophoretically transferred onto polyvinylidene fluoride membranes (Millipore, Billerica, MA, USA). The membranes were probed with mouse anti-EBAG9 monoclonal antibody12, rabbit anti-CD9 polyclonal antibody (sc-9148, Santa Cruz Biotechnology, Santa Cruz, CA, USA), rabbit anti-vimentin polyclonal antibody (SAB4503081, Sigma-Aldrich, St Louis, MO, USA), or rabbit anti-TM9SF1 polyclonal antibody (APR44683_T100, AVIVA Systems Biology, San Diego, CA, USA). For immuneprecipitation, cell lysates were incubated with the indicated antibody overnight at 4 °C. Then, protein G-sepharose beads (GE Healthcare Japan, Tokyo, Japan) was added to collect the immunocomplexes for an additional 1 h. The pellets were washed three times with lysis buffer and subjected to western blot analysis.
Total RNAs were extracted from prostate cancer LNCaP cells using ISOGEN reagent (Nippon Gene, Toyama, Japan), and first-stand cDNA was generated with 1 μg of total RNA using SuperScript III reverse transcriptase (Life Technologies) and oligo(dT)20 primer. To evaluate the expression levels of Cd8, VIM, SNAI1, SNAI2, EBAG9, TM9SF1, IFNG, IL10R, GZMB, and CXCR3, quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was performed by StepOnePlus Real-Time PCR system (Life Technologies) using specific primers (sense and antisense, respectively): mouse Cd8, 5′- GCTACCACAGGAGCCGAAAG-3′ and 5′-TGGGCTTGCCTTCCTGTCT-3′; human VIM, 5′-TGGATTCACTCCCTCTGGTTG-3′ and 5′-CGTGATGCTGAGAAGTTTCGTT-3′; SNAI1, 5′-CTAGGCCCTGGCTGCTACAA-3′ and 5′-TCTGAGTGGGTCTGGAGGTG-3′; SNAI2, 5′-CGGACCCACACATTACCTTG-3′ and 5′-TGACCTGTCTGCAAATGCTCT-3′; EBAG9, 5′-GGGAGCACAGGTTTCTCTAGT-3′ and 5′-CCTGCCAGGTATCTAAGTCAC-3′; TM9SF1, 5′-ATGACCTGGCTCGGTACAAC-3′ and 5′-TGTCACCCTGGTCAAAGTCA-3′; IFNG, 5′-AGCTCTGCATCGTTTTGGGTT-3′ and 5′-GTTCCATTATCCGCTACATCTGAA-3′; IL10R, 5′-GAAGACCGAGGCCATGAGG-3′ and 5′-GGCTGAATTTGCAGATGAGCA-3′; GZMB, 5′-CTGATACGAGACGACTTC-3′ and 5′-GGATTATAGGCTGGATGG-3′; CXCR3, 5′-GTCCTTGAGGTGAGTGACCA-3′ and 5′-AGCACGAGTCACTCTCGTTT-3′. Human GAPDH was used as an internal control47.
EVs isolation and uptake assay
EVs were prepared from the supernatant of LNCaP cells stably expressing EBAG9 or empty vector cultured in media without FBS using supercentrifugation as described48.
The EVs were labeled using the PKH67 green fluorescent labeling Kit (Sigma-Aldrich Japan, Tokyo, Japan) according to the manufacturer’s instruction. To examine uptake of PKH67-labeled EVs in LNCaP or MOLT4 cells, cells were incubated with PKH67-labeled EVs for the indicated times and fixed with 4% paraformaldehyde. Cells were costained with Cy3-labeled anti-vimentin antibody (Santa Cruz Biotechnology) and 4′,6-diamidino-2-phenylindole (DAPI).
The EVs prepared from LNCaP cells stably transfected with EBAG9 or empty vector were preincubated with EBAG9 monoclonal antibody12 or mouse normal IgG for 2 h at 4 °C. MOLT4 cells were cultured with the preincubated EVs in RPMI containing no FBS for 2 days. Then, MOLT4 cells were washed with PBS and plated at a density of 500 cells/well in 96 well-plate in phenol-red free RPMI containing no FBS together with 5000 LNCaP cells. After 2 days, cytotoxicity was assayed using CytoTox 96 non-radioactive cytotoxicity assay (Promega, Madison, WI, USA) and absorbance was measured at 490 nm. Experiments were done in quadruplicate. The results are shown as mean ± SD (n = 4). Statistical analysis was carried out using two-sided Student’s t-test. **P < 0.01.
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The authors thank Dr. Tomohiko Urano for generating LNCaP cells stably transfected with EBAG9 and empty vector. This work was supported in part by Grants of the P-DIRECT and P-CREATE from the Japan Agency for Medical Research and development, AMED; Cell Innovation Program and “Support Project of Strategic Research Center in Private Universities” from the MEXT, Japan; by Grants from the Ministry of Health, Labor, and Welfare, the JSPS (23791783, 16K15496, and 16K09809), the advanced research for medical products Mining Program of the NIBIO, and the Takeda Science Foundation.
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The authors declare that they have no competing interests.
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Miyazaki, T., Ikeda, K., Sato, W. et al. Extracellular vesicle-mediated EBAG9 transfer from cancer cells to tumor microenvironment promotes immune escape and tumor progression. Oncogenesis 7, 7 (2018). https://doi.org/10.1038/s41389-017-0022-6
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