Although one of the first comprehensive examinations of long non-coding RNA (lncRNA) expression was performed in human CD8 T lymphocytes, little is known about their roles in CD8 T cells functions during the progression of hepatocellular carcinoma (HCC). Here, we show that Lnc-Tim3 is upregulated and negatively correlates with IFN-γ and IL-2 production in tumor-infiltrating CD8 T cells of HCC patients. Lnc-Tim3 plays a pivotal role in stimulating CD8 T exhaustion and the survival of the exhausted CD8 T cells. Mechanistically, Lnc-Tim3 specifically binds to Tim-3 and blocks its interaction with Bat3, thus suppressing downstream Lck/ NFAT1/AP-1 signaling, leading to nuclear localization of Bat3, and enhancing p300-dependent p53 and RelA transcriptional activation of anti-apoptosis genes including MDM2 and Bcl-2. In summary, Lnc-Tim3 promotes T cell exhaustion, a phenotype which is correlated with compromised anti-tumor immunity, suggesting that Lnc-Tim3 and its associated signaling pathways may influence the outcome of cancer therapies aimed at modulating the acquired immune system.
Hepatocellular carcinoma (HCC) is an inflammation-related cancer and the third leading cause of cancer-related death worldwide1. It is known that persistent inflammation exacerbates HCC development2. The evidence demonstrates that immune checkpoint molecules play an important role in immune evasion of HCC. Immunological studies are revolutionizing HCC immunotherapy3. The presence of tumor-infiltrating lymphocytes (TILs) is responsible for HCC immunogenicity4. Generally, most tumor cells express antigens that can be recognized by CD8 T cells, which trigger antitumor immune responses. These tumor-associated antigen (TAA)-specific CD8 T-cell responses positively influence the survival of HCC. The TAA-specific cytotoxic CD8 T cells are the key players in most immunotherapy studies in HCC5. However, TAAs-specific CD8 lymphocytes from TILs produce less IFN-γ than ones in peripheral blood, indicating the CD8 T cells display exhaustion in tumor microenvironment4,6. Accordingly, it has been proposed that an overcoming of immunosuppressive intratumor environment might potentially restore successful antitumor immunity.
Immune checkpoint molecules contribute to HCC immunosuppressive through suppressing the anti-tumor immune response7. T cell immunoglobulin mucin 3 (Tim-3, HAVCR2, Gene ID: 84868, located in chromosome 5), a member of immune checkpoint proteins, acts as an inhibitory receptor for T cells8. The interaction of Tim-3 with its ligand, galectin-9 (Gal-9), induces cell death. Tim-3 has been found in differentiated IFN-γ-producing CD4+ T helper type 1 and CD8+ T cytotoxic type 1 cells9. It has been reported that Tim-3 is mostly expressed on CD8 TILs of solid tumor10. However, Tim-3 does not contain any obvious inhibitory signaling motifs and leads to augmentation of T-cell receptor (TCR)-dependent signaling pathways in T cells. Moreover, the activating of Tim-3 can convey a death signal into T cells. How then do Tim-3+ exhausted CD8 T cells persist in HCC TILs?
More evidence shows that long non-coding RNAs (lncRNAs) regulate a diversity of biological functions. In the field of immunology, recent studies have shown extensive changes in lncRNAs expression during T cell development, differentiation, and activation11. The majority of the lncRNAs are expressed in a stage-or lineage-specific manner, however just few mRNAs display this property12. These facts suggest that T cell-specific lncRNAs play a vital role in the complexity of the T cell compartment13. For example, NeST is expressed in Th1 CD4 T cells, CD8 T cells, and natural killer cells. The nucleus-located NeST interacts with WDR5 and induces the expression of IFN-γ in activated CD8 T14. However, further efforts are needed to demonstrate whether lncRNAs exert their biological functions in T cells of tumor microenvironment.
In our previous studies, high-throughput screening has been used to explore the transcriptomic associations between lncRNAs and mRNAs in the TILs of HCC patients. In this study, the expression of Lnc-Tim3 (ENST00000443947.1, AC011288.2, located in chromosome 7) was upregulated in CD8 T cells from HCC TILs. Lnc-Tim3 correlates with the exhaustion of CD8 T lymphocytes and the correlated mechanisms are studied. The results indicate that Lnc-Tim3 binds to Tim-3 and leads to release of Bat3, thereby reducing the stimulation of Lck and its downstream AP-1/NFAT1 signaling. However, Lnc-Tim3 protects from Gal-9-mediated cell death. The results show that released Bat3 enhances the recruitment of p53 and RelA to p300 and facilitates subsequent transcription of anti-apoptotic genes. Altogether, Lnc-Tim3 promotes CD8 T cell exhaustion and survival, a phenotype which is correlated with compromised anti-tumor immunity.
Upregulated Lnc-Tim3 correlates with the exhaustion of CD8 T lymphocytes
Tim-3 has been shown to negatively regulate T-cell-dependent immune responses and was recently demonstrated to be associated with the phenomenon of immune exhaustion15. Others have reported that Tim-3 is mainly expressed on CD8 TILs in mice bearing solid tumors and human cytotoxic T type 1 (TC1) CD8 cells16. Tim-3+ TILs exhibit the most severe exhausted phenotype as defined by failure to proliferate and produce IL-2, TNF, and IFN-γ10. To examine a potential role for Tim-3 in T cell exhaustion in HCC, we first examined the expression of Tim-3 in CD8 T cells via flow cytometry analysis. We found that the percentages of Tim-3+ CD8 T cells was highly upregulated in tumor-infiltrating T cells compared to the peripheral blood T cells from HCC patients and healthy controls (Fig. 1a). In our previous study, transcriptome profiling of lncRNA-mRNA co-expression networks comparison between HCC TILs and peripheral blood lymphocytes (PBLs) have been done17. In the present study, we mainly focused on the dysregulated lncRNAs and related lncRNA-mRNA co-expression networks in tumor-infiltrating CD8 T cells. According to our previous study, we found Tim-3 and Lnc-Tim3 (ENST00000443947.1) showed the greatest difference. Both the mRNA and lncRNA screening indicated that the different expression of the candidate RNAs mainly occurred in CD8 T cells, rather than CD4 T cells. To ensure that the novel candidates that we predicted did not encode proteins, we used GeneID and CPAT to measure the protein-coding potential and the ORF size in Lnc-Tim3 sequence (Fig. 1b). To further understand the functions of the Lnc-Tim3, we first conducted real-time PCR assay to confirm its abnormal expression in the CD8 T cells from 40 individuals with HCC and 40 healthy controls. We found that Lnc-Tim3 was highly upregulated in tumor-infiltrating T cells compared to the peripheral blood T cells from HCC patients and healthy controls (Fig. 1c). Moreover, further flow cytometry analysis confirmed that a negative correlation was identified between Lnc-Tim3 expression and the percentage of IFN-γ+ CD8 T cells in the tumor-infiltrating CD8 T cells of HCC patients (Fig. 1d), suggesting that the presence of Lnc-Tim3 is associated with the exhaustion of CD8 T lymphocytes.
Lnc-Tim3 specifically binds to the intracellular (IC) domain of Tim-3
We next used a RNA pull-down assay with biotinylated Lnc-Tim3 to search for potential Lnc-Tim3-interacting proteins. Mass spec analysis of pull-down proteins revealed that the previously predicted Lnc-Tim3 partner, Tim-3, was a Lnc-Tim3-associated protein (Fig. 2a). On the basis of these results, the bioinformatic software catRAPID was used to predict the potential Tim-3 binding regions in Lnc-Tim3 and the potential protein-binding domains for Lnc-Tim3 in Tim-3 (Fig. 2b). As shown in Fig. 2b, c, the predicted region (nucleotides 251 to 302) in the Lnc-Tim3 were predicted to bind to Tim-3 and the amino acids between 226 and 277 in the IC domain of Tim-3 were suggested to be the most possible Lnc-Tim3 binding domain. Our pull-down results showed that deletions in the 251 to 302 regions of Lnc-Tim3 abrogated its binding ability to Tim-3 (Fig. 2d). Additionally, the deletion of the Lnc-Tim3 binding region (nucleotides 251 to 302) or Tim-3 binding region (amino acids 226 to 277) did not affect the levels of Lnc-Tim3 or Tim-3 protein, respectively (Fig. 2e,f). The results suggested that deletion mutant of Lnc-Tim3 and Tim-3 did not affect their stability. Furthermore, RNA immunoprecipitation (RIP) assays revealed that only anti-HA (wild type Tim-3) antibodies specifically precipitated Lnc-Tim3, but deletions in the amino acids 226 to 277 of Tim-3 abrogated its binding ability to Lnc-Tim3 (Fig. 2g). Taken together, our results suggest that Lnc-Tim3 specifically interacts with Tim-3 and that the predicted region (251 to 302) of Lnc-Tim3 is important for Lnc-Tim3 to bind to Tim-3.
Lnc-Tim3 promotes CD8 T cell exhaustion but protects from galectin-9-mediated cell death
In other studies, the IC domain is required for Tim-3 signaling to T-cell activation pathways in a redundant fashion15. To further understand the functions of the Lnc-Tim3, Tim-3+CD8 T cells were sorted by flow cytometry from TILs of HCC patients. Subsequently, a series of in vitro experiments were performed to investigate the pro-exhaustion effects of Lnc-Tim3 in CD8 T cells. Silencing of endogenous Lnc-Tim3 by a lentivirus expressing Lnc-Tim3-targeting shRNA was employed in the Lnc-Tim3highTim-3+CD8 T from TILs, and we found that Lnc-Tim3-sliencing cells produced greater amounts of IFN-γ (Fig. 3a, left) and interleukin-2 (IL-2) (Fig. 3b) than control cells after treatment with anti-TCR/anti-CD28 beads, interleukin-12 (IL-12), and peptide cocktail. Additionally, Silencing of Lnc-Tim3 resulted in increasing the percentage of IFN-γ secreting CD8 T cells (Fig. 3a, right) and significantly more IFN-γ secreting (Fig. 3c). Furthermore, we lentivirally overexpressed wild type and mutant (Δ251-302) forms of Lnc-Tim3-HA in Lnc-Tim3lowTim-3+CD8 T from TILs, and found that Lnc-Tim3-WT, but not Lnc-Tim3-Δ, strikingly reduced the amounts of IFN-γ (Fig. 3d, left) and IL-2 (Fig. 3e), the percentage of IFN-γ secreting CD8 T cells (Fig. 3d, right) and IFN-γ secretion (Fig. 3f) after treatment with anti-TCR/anti-CD28 beads, interleukin-12 (IL-12), and peptide cocktail. It is known that triggering of Tim-3 can transmit a death signal into T cells18. To directly assess the effect of Lnc-Tim3 on signaling through the galectin-9–Tim-3 axis, we assessed the ability of galectin-9 to induce the death of Lnc-Tim3 (wild type and mutant)-overexpressing Jurkat T cells. Overexpression of Lnc-Tim3WT, but not Lnc-Tim3Δ251-302, showed a lower percentage of Tim-3-transfected Jurkat T cells underwent cell death than control after galectin-9 treatment (Fig. 3g).
Lnc-Tim3 induces an exhausted-like phenotype via suppressing Tim-3–Bat3 signaling
To confirm the importance of Lnc-Tim3 for its negative regulatory effects on T cell exhaustion and T cell signaling, we assessed the expression of exhaustion-associated markers of Lnc-Tim3 (wild-type and mutant)-overexpressing Jurkat T cells. Overexpression of Lnc-Tim3WT, but not Lnc-Tim3Δ251-302, upregulated a number of exhaustion-associated markers, such as the transcription factors LAG3, PRDM1 and PBX3 (Fig. 4a). A later investigation has shown that Bat3 binds to IC domain of Tim-3 and recruits the catalytically active form of Lck (phosphorylated at Tyr394 (pTyr394)), thereby forming an IC molecular complex with Tim-3 that preserves and potentially promotes T cell signaling and represses Tim-3-mediated cell death and exhaustion. To confirm that Lnc-Tim3 is able to inhibit Bat3–Tim-3 interaction via binding to the IC domain of Tim-3, we overexpressed Bat3-Myc and Tim-3-HA constructs in HEK 293 T cells and found that Tim-3 coimmunoprecipitated with Bat3 (Fig. 4b). Using the Lnc-Tim3 deletion constructs Lnc-Tim3Δ251–302, we identified residues 251–302 of Lnc-Tim3 as being crucial for mediating inhibiting Bat3–Tim-3 interaction (Fig. 4b). Bat3 recruits the catalytically active form of Lck (pLck Tyr394), thereby forming an IC molecular complex with Tim-319. Further, we observed the levels of pLck Tyr394 and pLck Tyr505 in Jurkat T cell that were lentivirally overexpressed of Lnc-Tim3WT or Lnc-Tim3Δ251–302. The results showed that the catalytically active form of Lck (pLck Tyr394) was reduced and a substantial amount of catalytically inactive Lck (pLck Tyr505) accumulated in Lnc-Tim3-WT transfected Jurkat T cells (Fig. 4c). In contrast, Δ251–302 restored the inhibitory effects of Lnc-Tim3 on Lck activation (Fig. 4c). Similarly, the inhibitory effects of Lnc-Tim3 on Lck activation was also confirmed in Tim-3+CD8 T cells from TILs of HCC patients (Fig. 4d). Notably, Bat3 could not pull down the catalytically active form of Lck (pTyr394) only in Lnc-Tim3 transfected Jurkat T cells (Fig. 4e). These data indicate that the inhibition effects of Lnc-Tim3 on Tim-3–Bat3 signaling is dependent on the predicted region (251 to 302). The cytoplasmic tail of Tim-3 is critical inducing NFAT1 and AP-1 signaling activation15. Interestingly, we observed that wild type Lnc-Tim3 reduced the NFAT1 and AP-1 activation compared to control in Jurkat T cells with anti-TCR/CD28 stimulation. However, the Lnc-Tim3Δ251–302 led to a much more dramatic restoration of NFAT1 and AP-1 activation (Fig. 4f).
Lnc-Tim3 leads to nuclear localization of Bat3 and enhances p300-dependent p53 and RelA transcriptional activation
Bat3 interacts with histone acetyltransferases p300 in the cytoplasm and is responsible for p300 nuclear translocation via the nuclear localization signal at its C terminus20. To determine whether the released Bat3 could form a complex with p300 and increase its nuclear translocation, we prepared nuclear and cytosolic fractions from Jurkat T cells that had been transfected with either Lnc-Tim3WT or Lnc-Tim3Δ251–302 and Tim-3-HA. Lnc-Tim3WT, but not Lnc-Tim3Δ251–302, leads to the Bat3 and p300 proteins nuclear translocation (Fig. 5a). To confirm these biochemical findings at the cellular level, we investigated the subcellular localization of Bat3 and p300 in Jurkat T cells. In Lnc-Tim3WT transfected cells, Bat3 and p300 could colocalized in the nucleus (Fig. 5b). However, in Lnc-Tim3Δ251–302 transfected cells, Bat3 and p300 was stained only very weakly in the nucleus (Fig. 5b). Bat3 enhances the recruitment of p53 to p300 and facilitates subsequent p53 acetylation21. The interaction of the RelA subunit of NF-kB with CBP/p300 is vital for RelA-dependent gene transcription22. The subcellular localization of p300 and p53 was assessed by immunofluorescence and we found that p53 was detected in nuclei and colocalized with p300 after transfection with Lnc-Tim3WT. In contrast, Δ251–302 of Lnc-Tim3 did result in colocalization of p53 and p300 (Fig. 5c). Similarly, Lnc-Tim3WT, but not Lnc-Tim3Δ251–302, promoted the colocalization of RelA and p300 in the nuclei (Fig. 5d). Furthermore, we found that Lnc-Tim3 increased p53 acetylation and the expression of p21, MDM2, and Bcl-2. However, deletions predicted region (251–302) of Lnc-Tim3 abrogated the transcriptional activation of these genes (Fig. 5e). These results suggested that upregulated Lnc-Tim3 could promote expression of anti-apoptosis proteins, thereby contributing to the survival of Tim-3+ exhausted CD8 T cells.
Immunotherapy is an attractive choice to decrease the risk of relapse through eliminating micrometastatic residual disease after surgical or percutaneous ablation in HCC3,23. Immune checkpoint inhibitors, such as ipilimumab (anti-CTLA-4), nivolumab (anti-PD-1) and pembrolizumab (anti-PD-1), which have already received regulatory approval24,25. Furthermore, several properties of Tim-3 make it a perfect target for the next generation of immunotherapy. For example, its selective expression on intratumoral T cells may allow for more precise therapy via the targeting of tumor-infiltrating T cells, potentially reducing non-specific toxicity26. However, the underlying mechanisms are not well understood and seemingly even contradictory to well-established T cell-stimulating function of Tim-327.
LncRNAs exhibit dynamic expression in cell-type, developmental-stage and context-specific manners to coordinate several aspects of immune function in the immune system28. Therefore, it is critical for us to know more about lncRNAs biological functions and elucidate the mechanism by which lncRNAs exert their immunoregulatory effects. LncRNA-CD244 recruits the EZH2 complex to IFN-γ and TNF genes promoter, thus suppressing the expression of IFN-γ and TNF-α in CD8 T cells29. Linc-CCR2-59AS significantly promotes the migration of effector Th2 cells into the lung of C57BL/6 mice30. In our previous study, we have extracted T cells from both blood and the tissues of three patients with HCC and the blood of three healthy volunteers. The lncRNAs and mRNAs expression profiles of CD3 T cells has been established. Among them, Lnc-EGFR promotes HCC immune evasion via stimulating T-regulatory cells differentiation17. In this study, we focus on the dysregulated lncRNAs and related lncRNA-mRNA co-expression networks in tumor-infiltrating CD8 T cells. We found that Lnc-Tim3 (ENST00000443947.1) was upregulated and negatively correlated with the percentage of IFN-γ+ CD8 T cells in the tumor-infiltrating CD8 T cells of HCC patients.
T cell exhaustion is identified as a natural mechanism for restricting immune pathology, although it may be desirable to circumvent this mechanism to help eliminate tumors31. Up to date, transmembrane proteins PD-1, LAG3, and Tim-3 are considered as the markers of exhausted T cells32. However, Tim-3 also has been found to actually increase signaling downstream of TCR/CD3, at least under acute conditions33. Interestingly, we found that upregulated Lnc-Tim3 was correlated with the exhaustion of CD8 T lymphocytes. It has been verified that Bat3 binds to the IC domain in the C-terminal tail of Tim-3, thus recruiting the catalytically active form of Lck (pLck Tyr505), promoting T cell signaling activation, and repressing CD8 T cell exhaustion19. In our study, the results show that Lnc-Tim3 specifically binds to the IC domain of Tim-3. Tim-3 leads to release of Bat3 from the Tim-3 tail, thereby promoting Tim-3-mediated T cell inhibition by accumulating catalytically inactive form of Lck (pLck Tyr505). Bat3-overexpressing Th1 cells produced greater amounts of IFN-γ and IL-2 and significantly more IFN-γ19. Similarly, our study demonstrates that Lnc-Tim3WT, but not Lnc-Tim3Δ251–302, strikingly reduced the amounts of IFN-γ and IL-2, the percentage of IFN-γ secreting CD8 T cells, and IFN-γ secretion. Src family tyrosine kinase Lck has two different forms, inactivated form (pLck Tyr505) and activated form (pLck Tyr394)34. The engagement of the TCR and coreceptor is critical for T-cell immune response initiation. Activation of Lck (pLck Tyr394) is central to the initiation of TCR signaling pathways35. Activated Lck phosphorylates ZAP-70 that, in turn, activates the transcription factors NFAT and AP-1, thereby driving T-cell immune response to antigen36. Interestingly, we observed that wild type Lnc-Tim3 reduced the activation of transfactor NFAT1 and AP-1. However, deletions predicted region (251–302) of Lnc-Tim3 led to a much more dramatic restoration of NFAT1 and AP-1 activation. These results suggest that Lnc-Tim3 induces an exhausted-like phenotype via suppressing Tim-3–Bat3 signaling and downstream signaling pathway NFAT1 and AP-1 in CD8 T cells.
It has been studies that Tim-3 causes a replicative senescent of CD8 lymphocytes from HCC TILs. Bat3 interacts with histone acetyltransferases p300 in the cytoplasm and is responsible for p300 nuclear translocation via the nuclear localization signal at its C terminus20,21. According to the results, we discover that the interactions between Lnc-Tim3 and Tim-3 leads to release of Bat3 from the Tim-3 IC tail and the released Bat3 is then free to form a complex with p300, thereby increasing its nuclear translocation. Nuclear Bat3 enhances the recruitment of p53 to p300 and facilitates subsequent acetylation of p53 and transcription of p21. The acetylation of p53 modulates p21-dependent cell-cycle arrest37,38. It was revealed that interaction between p53 and p21 could inhibit interaction of cyclin-A/CDK2 complex with blocking the cell cycle through G1/S39,40. These results suggest that Lnc-Tim3 may induce the replicative senescent of CD8 T cells in HCC TILs via promoting the formation of p300/p53/p21 complex.
In HCC, IFN-γ derived from TILs induced Gal-9 expression by Kupffer cells and Tim-3+ T cells co-localized with Gal-9+ Kupffer cells within the tumor41. However, Tim-3+ exhausted CD8 T cells persist in HCC TILs6. Interestingly, upregulated Lnc-Tim3 could promote expression of anti-apoptosis proteins, thereby contributing to the survival of Tim-3+ exhausted CD8 T cells in HCC. In our study, Bat3 enhances the recruitment of RelA to p300 and facilitates subsequent transcription of MDM2 and Bcl-2. RelA has an important role in inflammatory response and T cell survival through regulating the activation of related-genes42. Furthermore, CBP/p300 can recruit RelA to its target promoter sites22. Additionally, RelA binds to the κB2 site in the MDM2 P1 promoter and induces MDM2 transcriptional activation. MDM2 blocks Bim-dependent apoptosis via binding and inhibition of p73, thus contributing to the survival of activated T cells43. Furthermore, RelA promotes the survival of T cells also by upregulating the anti-apoptotic protein Bcl-244,45.
In summary, we have revealed that Lnc-Tim3 links CD8 T cells exhaustion and HCC. Lnc-Tim3 specifically binds to the IC tail of Tim-3, thereby leading to release of Bat3 from the Tim-3 tail, accumulating catalytically inactive form of Lck (pLck Tyr505), suppressing downstream signaling pathway NFAT1 and AP-1 in CD8 T cells. Additionally, the released Bat3 forms a complex with p300 and increases its nuclear translocation, leading to recruitment of p53 and RelA to p300, promoting cell cycle arrest, and protecting from death in CD8 T cells (Fig. 6). These data imply an important role of Lnc-Tim3 in inducing CD8 T cells exhaustion, a phenotype which is correlated with compromised anti-tumor immunity. Since Tim-3 is considered to be an ideal target for the next generation of immunotherapy, these findings might suggest that Lnc-Tim3 and its associated signaling pathways may influence the outcome of cancer therapies aimed at modulating the acquired immune system.
Materials and Methods
Blood or tissue samples from 40 healthy volunteers and 55 HCC patients who received treatment between May 2014 and May 2016 at The First Affiliated Hospital of Nanjing Medical University (Nanjing, Jiangsu, China) were used for isolation of peripheral or tissue-infiltration lymphocytes. None of the patients had received anticancer therapy before surgery, and individuals with concurrent autoimmune disease, HIV, or syphilis were excluded. Clinical characteristics were classified according to the guidelines of Union for International Cancer Control (UICC TNM). All experiments were performed in compliance with government policies and the Helsinki Declaration. The individuals were informed about the study and gave consent prior to the specimen collection. And the research has been approved by an ethics committee of the First Affiliated Hospital of Nanjing Medical University.
Data are presented as mean ± S.E.M. The Student’s t-test and analysis of variances were used to evaluate statistical differences in clinical characteristics. All the expression experiments we conducted in vitro were repeated at least three times with samples in triplicates. Pearson correlation analysis was used to analyze the relationship of associated factors. Statistical analysis was performed using STATA 9.2 and presented with the GraphPad prism software (CA, USA). In all cases, P < 0.05 was considered significant.
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This work was supported by grants from the State Key Program of National Natural Science of China (81430062 to B.S.); National Basic Research Program of China (2012CB910800 to B.S.); Jiangsu Provincial Natural Science Foundation-Youth Foundation (BK20170699); National Natural Science Foundation of China (81702323). This work also supported in part by the program for Development of Innovative Research Team in the First Affiliated Hospital of NJMU, and the Priority Academic Program of Jiangsu Higher Education Institutions. B.S. is Yangtze River Scholars Distinguished Professor.
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Journal of Hematology & Oncology (2018)