Increasing evidence shows that the anti-tumor functions of tumor-infiltrating T lymphocytes (TILs) were inhibited significantly, but the underlying mechanisms remain not fully understood. In this study, we found that 14-3-3ζ expression was up-regulated in hepatocellular carcinoma (HCC) cells and in TILs. TILs with 14-3-3ζ high-expression (14-3-3ζhigh) exhibited impaired activation (CD69), proliferation (Ki67) and anti-tumor functions compared to 14-3-3ζ low expression (14-3-3ζlow) TILs. Flow cytometry assay showed that compared with 14-3-3ζlow CD8+T cells, 14-3-3ζhigh ones exhibited higher frequency of exhausted phenotypes as measured by inhibitory receptors such as PD-1, TIM-3, LAG3, and CTLA-4. 14-3-3ζ overexpression inhibited the activity and proliferation of peripheral blood CD3+ T cells, deviated the differentiation of naive T cells from effector T cells to regulatory T cells. Moreover, we found that 14-3-3ζ expression levels in TILs correlated positively with those in HCC cells. Naive T cells co-cultured with HCC cells or the visible components of culture medium of HCC cells exhibited increased 14-3-3ζ expression. Stochastic optical reconstruction microscopy (STORM) and confocal assay showed that 14-3-3ζ-containing exosomes derived from HCC cells could be swallowed by T cells, suggesting that 14-3-3ζ might be transmitted from HCC cells to TILs at least partially through exosomes. In conclusion, our study for the first time demonstrated that 14-3-3ζ is up-regulated in and inhibited the anti-tumor functions of tumor-infiltrating T cells in HCC microenvironment and that 14-3-3ζ might be transmitted from HCC cells to T cells at least partially through exosomes.
14-3-3ζ was highly expressed in HCC cells and in TILs.
14-3-3ζ impaired the anti-tumor activity of TILs in HCC.
14-3-3ζ was associated with T cells exhaustion.
14-3-3ζ could be transmitted from HCC cells to TILs at least partially through exosomes.
Hepatocellular carcinoma (HCC) accounts for ninety percent of primary liver cancer, which is the fifth most common cancer and the second leading cancer death worldwide1. Increasing evidence has shown that in cancer immune microenvironment (IME), there is an increase in the number of immunosuppressive cells and in the meanwhile a decrease in the number and function of anti-cancer immunocytes2,3. Lymphocytes in peripheral blood mononuclear cells (PBMC) that infiltrate into tumor microenvironment are called tumor infiltrating lymphocytes, which are the main component of tumor IME4,5. Previous studies in HCC have demonstrated that the anti-tumor effects of T cells in tumor microenvironment decreased significantly, but the underlying mechanisms remain to be fully elucidated6,7.
14-3-3ζ, also called 14-3-3 protein zeta, has been reported to be highly expressed in HCC, and to promote the proliferation and epithelial-mesenchymal transition (EMT) of HCC cells8,9. Moreover, clinical study has shown that high expression of 14-3-3ζ in patients with HCC correlated with poor survival8,10. However the roles of 14-3-3ζ in tumor infiltrating T lymphocytes (TILs) have rarely been studied. Our preliminary data for the first time showed that the expression of 14-3-3ζ in HCC cells correlated significantly with that in TILs in HCC, however, the underlying mechanisms are obscure.
Exosome is a kind of tiny membrane vesicles that contains small molecules such as RNA, DNA and protein. It is exported by a diversity of cells and released into the microenvironment, which can then be up-taken by other cells11,12. Former studies have reported exosome as a transporter of diverse molecules associated with drug-resistance and metastasis in cancer13,14,15. So, we speculate that 14-3-3ζ might be delivered by exosomes from HCC cells to TILs and may affect the functionality of the latter. To testify our speculation, we designed this study to explore whether 14-3-3ζ is delivered from HCC cells to TILs through exosomes and to investigate the functional roles of 14-3-3ζ in TILs, in the hope of providing a new avenue to understand the mechanisms of dysfunctionality of T cells in HCC microenvironment.
14-3-3ζ was highly expressed in HCC cells and in TILs
Analysis based on Oncomine database of expression profiles with clinical cancer samples suggested that 14-3-3ζ mRNA level was significantly higher in HCC tissues than in cancer surrounding tissues (Fig. S1). In line with this, our results showed that 14-3-3ζ was highly expressed in HCC tissues compared to paracancerous tissues and normal liver tissues (Fig. 1a). Then, we constructed an inflammation-related HCC mouse model, positive staining of 14-3-3ζ cannot be observed until tumor was developed (Fig. 1b; Fig. S2).
Moreover, mRNA and protein expression levels of 14-3-3ζ in TILs were significantly increased relative to those in peripheral blood T cells (PBTC) (Fig. 1c, d). Next, we assayed the expression levels of 14-3-3ζ in CD4+ and CD8+ T cells separated from TILs or PBMC of HCC patients, respectively, the results of which showed that 14-3-3ζ protein and mRNA levels increased significantly in CD4+ and CD8+ T cells isolated from TILs compared to those from PBMC (Fig. 1e–h). In sum, 14-3-3ζ was highly expressed only in cancer cells and T cells in HCC microenvironment.
14-3-3ζ impaired the functions, proliferation and activation of T cells and regulate their differentiation
A total of 28 HCC tissues were subjected to immunohistochemistry (IHC) of 14-3-3ζ and were divided into 14-3-3ζhigh group (n = 14) and 14-3-3ζlow group (n = 14) (cut-off by median 14-3-3ζ expression level—relative integrated optical density (IOD) value of 14-3-3ζ assayed by western blot compared to that of GAPDH) (Fig. 2a). Analysis on clinicopathological features indicated that high-expression of 14-3-3ζ was associated with larger tumor size, poor tumor differentiation and terminal TNM stage (Table 1). The mRNA levels of the inflammatory cytokines (IFN-γ, IL-12, IL-2) and anti-inflammatory cytokines (TGF-β, IL-10, and IL-4) were assayed in TILs isolated from both groups (14-3-3ζhigh and 14-3-3ζlow). Interestingly, compared with 14-3-3ζhigh TILs, 14-3-3ζlow TILs expressed much higher levels of inflammatory cytokines but lower levels of anti-inflammatory cytokines (Fig. 2b).
CD3+ T cells, CD4+ T cells and CD8+ T cells isolated from HCC tissues (Fig. S3) in both groups (14-3-3ζhigh and 14-3-3ζlow) were stimulated with anti-CD3/CD28 beads for three consecutive days and then subjected to flow cytometry (FCM) to measure the percentage of Ki67+ cells and CD69+ cells. The results showed that CD3+ T cells, CD4+ T cells and CD8+ T cells isolated from 14-3-3ζhigh HCC tissue displayed decreased activity and proliferation ability compared with those from 14-3-3ζlow HCC tissue (Fig. 2c, d). Subsequently, the percentages of effector T cells (Teff) and regulatory T cells (Treg) in CD3+ T cells were assayed by FCM, the results of which showed that the percentage of Teff decreased whereas that of Treg increased in 14-3-3ζhigh group versus 14-3-3ζlow group (Fig. 3).
To further investigate the effects of 14-3-3ζ on the activation, proliferation and differentiation of T cells, we transfected naive T cells (CD45RA+CD197+) isolated from human PBMC with RV-NC (retro-virus packaged with empty plasmid) or RV-14-3-3ζ (retro-virus packaged with 14-3-3ζ overexpressing plasmid) (Fig. 4a–c). Subsequently, part of these cells were stimulated with anti-CD3/CD28 beads for three days and then subjected to FCM to measure the percentages of CD69+ cells and Ki67+ cells (Fig. 4d); and the other part of these cells were stimulated with IL-12 (10 ng/ml), IL-2 (10 ng/ml) or TGF-β (10 ng/ml) respectively for 72 h and then subjected to FCM to assay CD4, CD8, Foxp3, and IFN-γ. We found that overexpression of 14-3-3ζ significantly inhibited the activation and proliferation of T cells and deviated the differentiation of naive T cells from Teff to Treg cells (Fig. 4e), suggesting that 14-3-3ζ regulates the activation, proliferation, and differentiation of T cells.
14-3-3ζ high expression correlate with T cells exhaustion
Mounting evidence has demonstrated that T cell exhaustion is one of the major mechanisms of cancer immune evasion. As PD-1, TIM-3, LAG3 and CTLA-4 are well-established T cell exhaustion markers, we assayed these markers in CD8+ T cells isolated from TILs in 14-3-3ζhigh group and in 14-3-3ζlow group respectively. The results showed that there was a significantly higher percentages of PD-1+ T cells and PD-1+TIM-3+ T cells in 14-3-3ζhigh CD8+ T versus 14-3-3ζlow CD8+ T cells (Fig. 5a, b), indicating that 14-3-3ζ high expression correlated significantly with an exhausted phenotype of T cells.
14-3-3ζ was transmitted from HCC cells to TILs delivered by exosomes
IHC staining of HCC tissues and TILs showed that the percentage of 14-3-3ζ positive TILs (versus all TILs) positively correlated with that in HCC cells (versus all liver cells) (Fig. 6a). Real-time PCR and western blot assay in HCC cells and TILs separated from HCC tissues indicated that the protein level rather than the mRNA level of 14-3-3ζ in HCC cells correlated well with those in TILs, (Fig. 6b, c, Fig. S4).
To investigate the mechanisms underlying the correlation between the expression levels of 14-3-3ζ in TILs and in HCC cells, we transfected SMCC7721 cells (Fig. 6d), which have the low level of 14-3-3ζ expression in their exosome (Fig. 6e, f), with Lv-NC (lenti-virus packaged with empty plasmid) or Lv-14-3-3ζ (lenti-virus packaged with 14-3-3ζ overexpressing plasmid). Then we co-cultured naive T cells (after stimulation with CD3/CD28 beads for 3 days) with Lv-14-3-3ζ-transfected SMCC7721 cells, Lv-NC-transfected SMCC7721 cells (Fig. 6g, h, Fig. S5), visible components or invisible components of culture medium of these cells. The results showed that 14-3-3ζ expression levels were increased in naive T cells co-cultured with Lv-14-3-3ζ-transfected SMCC7721 cells and with visible components of cell culture medium of Lv-14-3-3ζ-transfected SMCC7721 cells (Fig. 7a–c). These results indicated that 14-3-3ζ-overexpressing HCC cells or their visible components of cell culture medium is responsible for the transmission of 14-3-3ζ from HCC cells to T cells.
As the visible components of cell culture medium were mainly composed of exosomes, we detected the level of 14-3-3ζ in exosomes isolated respectively from the serum of healthy individuals, serum of HCC patients, cell culture medium of MHCC97H cells (expressing relative higher level of 14-3-3ζ), Lv-shRNA transfected MHCC97H cells (Fig. 6d), SMCC7721 cells and Lv-14-3-3ζ transfected SMCC7721 cells. We found that the protein and mRNA levels of 14-3-3ζ were significantly higher in exosomes isolated from HCC serum compared to those from healthy serum. We found that in exosomes derived from 14-3-3ζ-overexpressing cells, the level of 14-3-3ζ is higher (Fig. 7d–f), which was in accordance with the former study16. We also found that naive T cells co-cultured with 14-3-3ζhigh exosomes produced lower level of IL-2 and IFN-γ, and showed higher level of PD-1 and TIM-3 expression than those co-cultured with 14-3-3ζlow exosomes (Fig. 7g, h). Immunofluorescence staining assay indicated 14-3-3ζ can transfer into T cells, and moreover, we observed that 14-3-3ζ-containing exosomes exported by HCC cells can be swallowed by T cells. (Fig. 8a–d).
These results suggested that 14-3-3ζ could be transmitted from HCC cells to TILs via exosomes.
In this study, we found that in HCC microenvironment, TILs with 14-3-3ζ high expression presented impaired anti-tumor function compared to those with 14-3-3ζ low expression. Overexpression of 14-3-3ζ deviated the differentiation of T cells from effective ones to regulatory ones. What’s more, we found that up-regulation of 14-3-3ζ in TILs was at least partially attributable to the up-take of 14-3-3ζ-containing exosomes exported from HCC cells.
Previous studies have suggested the oncogenic roles of 14-3-3ζ in diverse cancer types including HCC17,18. For example, 14-3-3ζ was upregulated in HCC and can promote HCC invasion and metastasis through binding to AXL (activity of the receptor tyrosine kinase Axl)9 or through interacting with αB-crystallin mediated by TGF-β and ERK signaling pathways8. However, to the best of our knowledge, the roles of 14-3-3ζ in T cell function were still not reported. Chimen, et, al. reported that PEPITEM, a peptide derived from 14-3-3ζ, inhibited T cell trafficking and thus reduce T cell recruitment into inflammation sites during chronic inflammation19, which suggest that 14-3-3ζ may affect T cell immunity in some way.
Our study for the first time found that the protein expression levels of 14-3-3ζ in HCC cells correlated positively with that in TILs, and that the expression levels of 14-3-3ζ in TILs of HCC were significantly higher than those in PBTC. To explore the effects of 14-3-3ζ expression levels on TILs function, we assayed the activity and functionality of TILs in 14-3-3ζhigh group and 14-3-3ζlow group. The results showed that the activation and anti-tumor activity of TILs in 14-3-3ζhigh group were significantly impaired compared to those in 14-3-3ζlow group, as evidenced by decrease excretion of cytotoxic cytokines. As CD8+ T cells are the major anti-tumor effector cells in TILs20,21,22, we assayed the exhaustion markers (PD-1, TIM-3, LAG3, CTLA-4)23,24,25 in CD8+ T cells isolated from 14-3-3ζhigh and from 14-3-3ζlow group. The results showed increased expression of T cell exhaustion markers (PD-1+TIM-3+)26,27 in CD8+ T cells from 14-3-3ζhigh group as compared to those from 14-3-3ζlow group, suggesting that 14-3-3ζ may contribute to CD8+ T cell exhaustion. Overexpression of 14-3-3ζ decreased the activation and proliferation of naive T cells and deviate the differentiation of the latter from effector T cells to regulatory T cells (Treg). These findings as a whole point to the conclusion that 14-3-3ζ impaired the anti-tumor activity of TILs in HCC.
As 14-3-3ζ expression in HCC cells correlated positively with that in TILs and the levels of 14-3-3ζ in TILs were significantly higher than those in PBTC, we speculated that the expression of 14-3-3ζ in TILs might be influenced by 14-3-3ζ in HCC cells through mechanisms such as direct contact transmission or indirect communications mediated by certain vehicles in the interstitial fluid like exosomes28,29.
To test our speculation, we co-cultured naive T cells respectively with HCC cells, visible components and invisible components of cell culture medium of 14-3-3ζ-overexpressing HCC cells. It has been previously reported that stromal cells uptake 14-3-3-sigma protein through an aminopeptidase N-dependent mechanism30, however, our results showed that 14-3-3ζ expression levels were increased in naive T cells co-cultured with 14-3-3ζ-overexpressing HCC cells or their visible cell culture components rather than with invisible cell culture components, suggesting that 14-3-3ζ in TILs is influenced by 14-3-3ζ in HCC cells, at least partially mediated by visible cell culture components. Electronic microscopy and stochastic optical reconstruction microscopy (STORM)31,32 demonstrated that these visible components comprise mainly of exosomes and vesicles. Next, we observed that 14-3-3ζ was detectable in exosomes isolated from these visible cell culture components and that these 14-3-3ζ-containing exosomes could be swallowed by T cells in co-culture. These results as a whole suggest that 14-3-3ζ could be transmitted from HCC cells to TILs at least partially delivered by exomoses.
However, there are still some limitations of our study that should be addressed by future studies. First, the mechanisms underlying the effects of 14-3-3ζ on TILs function remain to be investigated; second, the possibility of other means besides exosomes by which 14-3-3ζ was transmitted from HCC cells to TILs should not yet be excluded, such as direct contact transmission. Next, we will conduct sequencing studies to elucidate the signaling pathways involved in the functional roles of 14-3-3ζ in TILs, and will investigate other transmission means of 14-3-3ζ.
To sum up, our study for the first time demonstrate that 14-3-3ζ impaired the anti-tumor activity of TILs in HCC and that 14-3-3ζ could be transmitted from HCC cells to TILs at least partially through exosomes. To the best of our knowledge, ours is the first to elucidate the functional roles of 14-3-3ζ in T cells and the underlying mechanisms of up-regulated expression of in TILs. Our study offers a new angle to understand T cell dysfunction in HCC and may open a new avenue for the development of novel immunotherapeutic targets for HCC.
Materials and methods
Fresh HCC tissues, corresponding adjuvant noncancerous tissues, and HCC serum samples were collected from patients undergoing hepatectomy between Sep, 2016 and Feb, 2017. Peripheral blood samples were collected before hepatectomy. Healthy serum samples were randomly selected from patients receiving physical examination at the First Affiliated Hospital of Nanjing Medical University (Nanjing, China). The study was approved by our Institutional Ethics Committee and performed in accordance with the Helsinki Declaration and government policies. All participants have signed the written informed consent. Clinical and pathological characteristics were summarized in Table 1.
Male C57BL/6 mice were bred and maintained under specific pathogen-free conditions in the Laboratory Animal Center of Nanjing Medical University. Immature mice were intraperitoneal injected (ip) with 25 μg/g diethylnitrosamine (DEN) at two-week old for once and subsequently challenged with 0.5 μg/g CCl4 (ip) once a week from four-week old to the end. Mice were killed under ether anesthesia at design time point and tissue samples were carefully collected. All animals received humane care and all experiments were carried out according to the guidelines outlined in the Guide for the Care and Use of Laboratory Animals.
Cells and cell transfection
Human PBTC were cultured in RPMI-1640 medium (Invitrogen) supplemented with 10% heat-inactivated FBS, 100 U/ml penicillin, and 100 mg/ml streptomycin (Invitrogen). For lenti-virus construction, the 14-3-3ζ sequence was synthesized by GenScript Inc (China), short-hairpin RNA to interfere 14-3-3ζ in MHCC97H cells was purchased from (sc-29583, Santa Cruz, CA, USA), and then were inserted into lentiviral vector PCDH. For retrovirus construction, the 14-3-3ζ sequence was synthesized by GenScript Inc (China) and subcloned into retroviral vector pMXs. Retroviral particles were generated by 293 T cells and transfected into CD3+ T cells or naive T cells 24 h after activation with anti-human CD3/CD28 beads. Lentiviral particles were generated by 293 T cells, and transduced into SMCC7721 cells. Then, transductants were placed into puromycin-containing medium for 3 days before culture.
Isolation of lymphocyte, CD3+, CD4+, CD8+ T cells and naive T cells
Fresh human HCC tissues (the tissue volume was recorded) were obtained and maintained in phosphate-buffered saline (PBS), then cut into pieces and filtered through a 70 μm cell strainer (BD Biosciences) into a 50 ml Falcon tube. Human peripheral blood was collected from HCC patients or healthy volunteers (10 ml each). Single-cell suspensions were softly added to the surface of 10 ml Ficoll-Paque (GE Healthcare), then centrifuged at 400 × g for 30 min at 20 °C according to the manufacturer’s instructions. A portion of peripheral blood mononuclear (PBMC) or tumor infiltrating lymphocytes were used to separate T cells by using anti-human CD3, CD4, or CD8 beads, isolated cells were measured by subsequent flow cytometric analysis. For naive T cells separation, PBMC was labeled with anti-human CD45RA and CD197, then naive T cells (CD45RA+CD197+) were sorted with flow cytometry on BD ARIA III (BD Biosciences).
Stimulation of T cells
cRPMI-10 consisted of RPMI-1640 medium supplemented with 10% fetal bovine serum, antibiotic/antimycotic solution, and HEPES buffer (Sigma-Aldrich). Fetal bovine serum was from a single lot qualified for low background and high responses in flow cytometer assays.
T cells were resuspended at 1 × 106 viable cells per ml in cRPMI-10 medium. For stimulation, 2 × 105 cells/well were plated in polypropylene U-bottom microtiter plates in a total volume of 200 µl of RPMI-1640. They were stimulated for 8 h at 37 °C, 5% CO2, using 10 ng/ml phorbol 12-myristate 13-acetate (PMA, Sigma-Aldrich), 500 ng/ml ionomycin (Sigma-Aldrich) and 1 g/ml Brefeldin A (BFA, Sigma-Aldrich). After then, T cells were measured by detection of CD69 expression using flow cytometry or used for RNA extration.
Cells were stimulated with anti-CD3/CD28 beads (Thermo Fisher Scientific) at a 1:2 bead to cell ratio. Proliferation was then measured by detection of Ki67 expression using flow cytometry.
Real time polymerase chain reaction (PCR)
Total RNA was extracted from live cells or exosomes using TRIzol reagent (Invitrogen) according to the instructions and total RNAs (500 ng) were reverse transcribed using the PrimeScript RT Master Mix (Takara). The expression levels of 14-3-3ζ was deteced by quantitative real-time PCR using the SYBR Premix Ex Taq (Takara, Dalian, China) on the ABI Prism 7900HT (Applied Biosystems). The relative expression levels of 14-3-3ζ were normalized to GAPDH (for cells) or β-Actin (for exosomes). The reactions were incubated in a 384-well optical plate at 95 °C for 30 s, followed by 40 cycles of 95 °C for 5 s and 60 °C for 30 s. Related primer sequence was provided in Table S1.
Immunohistochemistry and western blot
For IHC, tissues were fixed in 4% paraformaldehyde overnight at 4 °C, processed by paraffin embedding, then sectioned into 5 mm3 slices, and dewaxed. Antigen retrieval was performed by heating the slides in the autoclave for 3 min using citrate buffer (pH6.0). The slides were incubated overnight at 4 °C with the following primary antibodies (diluted at 1/1000): anti-14-3-3ζ antibody (Cell signaling technology). Immunodetection was performed with a UltraSensitiveTM SP(Mouse/Rabbit) IHC Kit (Fuzhou Maixin Biotech.). Images were acquired using a microscope (Nikon, ECLIPSE 50i) equipped with software NIS Elements v4.0, and average IOD was obtained by randomly collecting and analyzing five fields per slide using Image-Pro Plus software v.5.0. Detection for each index was performed for at least three times.
For western blot assay, total proteins were extracted from cells or exosomes using radio-immunoprecipitation assay buffer plus fresh protease and phosphatase inhibitors (Beyotime), then quantified with the Bradford assay (Bio-Rad Laboratories). Equal amounts of protein samples (30 μg) were loaded to each lane, then separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS–PAGE) and subsequently transferred to a polyvinylidene fluoride membrane. Antibodies against 14-3-3ζ (Cell signaling technology), human reduced glyceraldehyde-phosphate dehydrogenase (GAPDH) (Cell Signaling Technology) and β-actin (Cell Signaling Technology) were used in immunoblotting. The integrated density of the bands was quantified using ImageJ software (NIH).
Exosomes in supernatant were collected from HCC cells cultured for 48-72 h. The supernatant of cell culture medium was collected, then centrifuged at 800 × g for 5 min, followed by centrifugation of 2000 × g for 10 min to remove cellular debris. Then, the media was filtered through a 0.2 μm pore strainer (Syringe filter), and then ultracentrifuged at 100,000 × g for 2 h at 4 °C. The pellet was washed with 35 ml 1 PBS, followed by a second step of ultracentrifugation at 100,000 × g for 2 h at 4 °C. Afterwards, the supernatant was discarded.
For serum exosomes isolation, serum was diluted in 1 × PBS and filtered through a 0.2 μm filter, then ultracentrifuged at 150,000 × g overnight at 4 °C. Next, the pellet was washed in 10 ml 1 × PBS followed by ultracentrifugation at 150,000 × g at 4 °C for 2 h. The pelleted (exosomes) was collected. Exosomes resuspended in 500 μl of Trizol were for RNA extraction, resuspended in 250 μl of lysis buffer (8 M Urea/2.5%SDS, 5 μg/ml leupeptin, 1 μg/ml pepstatin and 1 mM phenylmethylsulphonyl fluoride) for protein extraction or re-suspended in PBS for immunofluorescence staining.
Enzyme-linked immuno sorbent assay (ELISA) assay
Exosome suffering freezing and freeze-thaw cycles were used to extract protein for ELISA assay, which was performed with an ELISA Kit for 14-3-3ζ (R&D Systems Inc., Minneapolis, USA) according to the instruction.
For CD63 immunofluorescence label of exosomes, 4 μl of exosome specimens was diluted in 400 μl of PBS buffer mixed with 1 μl of primary antibody (1 mg/ml rabbit anti-CD63, Thermofisher Scientific). Samples the were incubated for 2 h at room temperature. For the blank control, the PBS buffer instead of the primary antibody was used. Then, the reaction solution was treated with ultrafiltration (50 Kda) at 6000 rpm for 20 min. The precipitation was collected and suspended in PBS. Next, 1 μL of secondary antibody (2 mg/ml Alexa Fluor 647 labeled Goat anti-Rabbit IgG, ab150079, Abcam) was added. The mixture was vigorously stirred for 1 h at room temperature and then treated with ultrafiltration (50 Kda) at 6000 rpm for 20 min to remove excess reagents. The precipitation was collected and resuspended in 400 μL of PBS for stochastic optical reconstruction microscopy (STORM).
To immunofluorescence label 14-3-3ζ, cells were fixed in fresh acetone followed by permeabilization in 0.2% Triton X-100/0.5% normal goat serum/PBS, then incubated with primary antibody against 14-3-3ζ (Cell signaling technology) and secondary antibodies labeled with FITC. DAPI was used for nuclear staining. The cells were visualized using Confocal Laser Scanning Microscope (Leica TCS SP8).
Uptake of exosomes
Exosomes were incubated in 1uM 1,1′-dioctadecyl-3,3,3′3′-tetramethylindocarbocyanine perchlorate (DiI, Thermofisher Scientific) for 20 min, followed by an additional round of PBS wash. PBS was then used to resuspend the exosomes for cell treatment. Cells were co-cultured with DiI-labeled exosomes for 2 h. To simultaneously label 14-3-3ζ, the immunofluorescence experiment followed a similar procedure as described above.
Flow cytometry assay
Isolated T cells were collected by centrifugation (330 × g, 5 min at 4 ℃) and cell counts were determined by using a Countess Counter (Invitrogen). For surface staining, cells were resuspended in PBS (with 2% FBS) containing the antibody, incubated on ice for 30 min, washed in PBS (with 2% FBS), and analyzed using flow cytometry. Flow cytometry assay was performed on CANTO II (BD Biosciences). For intracellular molecule detection, fixation and permeabilization buffers (eBioscience) were used according to the instructions. Data were collected on BD CANTO II (BD Biosciences) with FACSCanto software version 2.1 (BD). Antibodies used were described in Table S2.
All statistical analyses were performed using SPSS 18.0 (SPSS Inc, Chicago, IL, USA) software and presented with the GraphPad prism software (GraphPad Software, San Diego, CA, USA). FlowJo 7.6.1, https://www.flowjo.com/solutions/flowjo) was used to analyze and output the data of flow cytometry assay. Results of quantitative real-time PCR were expressed as mean ± S.E.M. Student’s t test. In all cases, P < 0.05 was considered significant.
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
This work was supported by grants from the National Key Research and Development Program of China (Grant Number: 2016YFC0905900 to B.S.); the State Key Program of National Natural Science Foundation (Grant Number: 81430062 to B.S.); Innovative Research Groups of National Natural Science Foundation (Grant Number: 81521004 to B.S.), the National Natural Science Foundation (Grant Number: 81772596 to X.-J. L.), and Graduate student research innovation project of Jiangsu Province in 2017, (Number: KYCX17_1243 to X.W.). This work was also supported in part by the Priority Academic Program of Jiangsu Higher Education Institutions. B.S. is Yangtze River scholars Distinguished Professor. We are also grateful to Dr. Guisheng Zhong’s lab in ShanghaiTech University for providing technical support with stochastic optical reconstruction microscopy (STORM).
About this article
Journal of Cancer Research and Clinical Oncology (2018)