T memory stem cells (TSCMs), which possess the properties of self-renewal and multipotency, have been observed to play a role in the pathogenesis of various severe diseases such as graft-versus-host disease, malignant melanoma, Chagas disease, as well as human immunodeficiency virus type 1 and simian immunodeficiency virus infections.1–13 Mouse CD8+ TSCMs are a well-identified subset of postmitotic CD44low CD62Lhigh T cells that express surface proteins, including stem cell antigen-1 (Sca-1), common interleukin (IL)-2, IL-15, receptor β-chain (CD122), as well as B-cell lymphoma protein-2 (Bcl-2) at high levels. It has been reported that TSCMs could be generated in vitro from naive T cells by activation of the Wnt, IL-7, or IL-15 signaling pathways.1,2,14 Blood-derived TSCMs have also been tracked in vivo in patients after gene therapy for human severe combined immunodeficiency disease.15 Similar to conventional memory T cells, CD8+ TSCMs can be detected in umbilical cord blood in humans.3 Although this phenomenon indicates a tropism for lymphoid tissues, the anatomic characterization of TSCM-cell niches has not been performed to date.
The bone marrow (BM) functions as the major reservoir and site of recruitment for hematopoietic stem cells (HSCs) as well as memory B and T cells by providing appropriate cellular niches.16–29 The common niche that supports HSCs or leukocytes in the BM is constituted by CXCL12+ stromal cells.30 Under certain conditions, the BM supports the homeostasis of naive T cells and pro-B cells.31–33 In addition, BM microvessels constitutively express prerequisite traffic molecules that support the recruitment of HSCs and conventional memory T cells, and potentially support the homing of other T-cell subsets.34 More importantly, the function of BM-resident CD8+ T cells is distinct from that of those residing in other organs. For instance, BM-resident CD8+ T cells from cancer patients elicit more efficient tumor-specific cytotoxicity than CD8+ T cells in peripheral blood (PB). Thus, T cells from the BM are regarded as potential resources for antitumor cellular therapy.35 Nevertheless, it is not known whether TSCMs, which constitute a distinct T-cell subset with the highest antitumor activity reported to date, accumulate in the BM.
In the present study, we demonstrate that the BM acts as a hub to which most tumor-specific CD8+ TSCMs relocate. Importantly, BM-resident TSCMs showed higher inhibitory activity against tumor growth than spleen (SP)-resident TSCMs in a B16 murine model, implying potential applications for immunotherapy against melanoma.
CD8+ T Memory Stem Cells Preferentially Reside in the BM
Although TSCMs are categorized as memory cells, they display a naive-like phenotype; these cells include CD62L+ CCR7+ CD45RO− CD45RA+ in humans and CD44low CD62Lhigh in mice.1–3,36 To determine whether TSCMs reside naturally in the BM, the expression levels of Sca-1 and CD122, which are typical markers used to distinguish TSCMs from naive T cells in mice, were first analyzed in CD44low CD62Lhigh CD8+ T cells (Fig. S1, Supplemental Digital Content 1, http://links.lww.com/JIT/A529). Significant elevation of the CD122high Sca-1high subset was observed in the BM-derived naive T-cell compartment (Fig. 1A, Fig. S2, Supplemental Digital Content 1, http://links.lww.com/JIT/A529) compared with those from other tissues, including SP, PB, and mesenteric lymph nodes (LN) (Fig. 1B). Thus, we hypothesized that CD122high Sca-1high TSCMs preferentially reside in the BM.
Well-defined TSCMs express not only high levels of CD122 and Sca-1 but also high levels of Bcl-2 and CXCR3.1,2 To validate whether these natural CD122high Sca-1high TSCMs in the BM are consistent with the previously well-defined TSCMs, the expression levels of Bcl-2 and CXCR3 were analyzed in CD122high Sca-1high TSCMs and CD122low Sca-1low naive T cells. As expected, the expression levels of both Bcl-2 and CXCR3 were higher in CD122high Sca-1high TSCMs than in naive CD8+ T cells (Figs. 1C, D, Fig. S3, Supplemental Digital Content 1, http://links.lww.com/JIT/A529).1,2 Similar to BM naive T cells reported previously, BM CD8+ TSCMs were also positive for CD127 expression (Fig. 1E).28 Despite the slightly lower expression of CD127 in BM CD8+ TSCMs, the difference was not statistically significant (Fig. S3, Supplemental Digital Content 1, http://links.lww.com/JIT/A529). It is interesting to note that, the expression of CD69 in BM-resident TSCMs was slightly higher than that of naive T cells (Fig. 1E, Fig. S3, Supplemental Digital Content 1, http://links.lww.com/JIT/A529). Of note, the canonical TSCMs reported previously in peripheral immune organs were αβ T cells.3 Therefore, to eliminate the potential interference of γδ T cells, which also reside in the BM and contain a fraction of cells expressing CD122 and Sca-1 molecules,37–39 the expression of T-cell receptor (TCR) chains was evaluated by flow cytometry. We found that CD122high Sca-1high TSCMs expressed TCRβ chains other than TCRγδ chains (Fig. 1F, Fig. S3, Supplemental Digital Content 1, http://links.lww.com/JIT/A529). In addition, to distinguish between TCMs, naive T cells and TSCMs in a postmitotic phenotype at the transcriptional level, we tested the expression of Ccr2, Ccr5, CD44, and Sca-1 (Ly6A/E) by quantitative real-time polymerase chain reaction (qRT-PCR) in accordance with previous reports1; results showed that the messenger RNA (mRNA) expression of Ccr2 in TCMs was much higher than in naive T cells and TSCMs, whereas the mRNA expression of Ccr5 in naive T cells was much lower than in TSCMs and TCMs (Fig. 1G). It is notable that the mRNA expression of CD44 was lower in TSCMs than that in TCMs but the mRNA level of Sca-1 (Ly6A/E) was significantly higher than that in naive T cells, which was consistent with the previous report (Fig. 1G).1 According to previous reports, cells with stem cell properties, including HSCs and TCMs, are most likely in the resting stage.20,26,27 In order to verify the stem cell properties of TSCMs, we examined the cell cycle of naive T cells, TSCMs, and TCMs (Fig. 1H, Fig. S4, Supplemental Digital Content 1, http://links.lww.com/JIT/A529). Measurement of DNA content showed that BM CD8+ TSCMs were stalled in the G0/G1 cell interphase and resting state; these findings were almost consistent with those for BM memory T cells, as indicated by previous reports (Fig. 1H).25,40 In addition, we examined other factors (Klf-7, Tcf-1, Lef-1, β-catenin) involved in the regulation of stemness of cells by qRT-PCR (Fig. 1G). The qRT-PCR data indicated that the mRNA expression of Tcf-1, Lef-1, and β-catenin in BM-resident TSCMs was notably higher than that in naive T cells (Fig. 1G). Collectively, these observations further support that BM-enriched CD122high Sca-1high naive-like CD8+ T lymphocytes can be identified as TSCMs that naturally inhabit the BM.
BM-resident CD8+ TSCMs Vigorously Respond to a Blood-borne Antigen
CD8+ TSCMs have been shown to elicit rapid immune responses upon antigen rechallenge.3,41 To investigate the immune responses of CD8+ TSCMs in situ, the purified naive T cells (CD8+ CD44low CD62Lhigh CD122low Sca-1low), TCMs (CD8+ CD44high CD62Lhigh), and TSCMs (CD8+ CD44low CD62Lhigh CD122high Sca-1high) from the BM of OT-Imice (CD45.2+) were adoptively transferred into congenic mice (CD45.1+), respectively, followed by antigen stimulation by ovalbumin (OVA) immunization (Fig. 2A, Fig. S5, Supplemental Digital Content 1, http://links.lww.com/JIT/A529). Flow cytometric analysis showed that the BM TSCMs displayed significantly higher levels of cell proliferation and interferon-γ (IFN-γ) production than BM TCMs and BM naive T cells (Figs. 2B, C). In addition, to test the downstream differentiation potential of TSCMs upon antigen exposure, we compared the frequencies of BM CD44+ T cells in naive T-cell-transferred or TSCMs-transferred recipient mice. As expected, we detected larger numbers of CD45.2+ CD44+ CD8+ T cells in TSCMs-transferred recipient mice (Fig. 2D), which indicated that the transferred CD8+ TSCMs were capable of differentiation into conventional memory or effector T cells more rapidly. These results indicate that BM-enriched CD122high Sca-1high TSCMs response to a blood-borne antigen efficiently.
Preferential Migration of CD8+ TSCMs to the BM
Owing to the limitation of low cell number of natural CD8+ TSCMs from wild-type (WT) mice, it was not practical to obtain the required cell numbers from WT mice on a large scale for investigation of the preferential migration of TSCMs to the BM. Although β-catenin signaling was not found to regulate the generation of memory T cells and inhibit T-cell proliferation, TSCMs could be generated efficiently from naive T cells in vitro with the glycogen synthase kinase-3β inhibitor TWS119 (a compound that induces TSCM cells by a mechanism of action that is currently debated) as previously reported.42,43 The naive T cells and in vitro-generated TSCMs cells with TWS119 were isolated by flow cytometry (Fig. S6, Supplemental Digital Content 1, http://links.lww.com/JIT/A529). Subsequently, we labeled naive T cells and TSCMs with CMTPX and then mixed with equivalent carboxyfluorescein succinimidyl ester (CFSE)-labeling SP cells, which served as a reference. The mixed cells were injected into recipient mice. After 6 hours, we detected the ratios of CMTPX-positive and CFSE-positive cells, and calculated the homing index (HI). The results showed that the HI of TWS119-induced TSCMs in the BM was ∼3-fold higher than that of those induced in the SP (Fig. 3A). To accurately compare the homing of each subset and avoid the off-target effects of small-molecule inhibitors, TSCMs were generated by stimulation of Wnt3A protein in vitro, and the frequency of each subset in the BM was determined. Flow cytometric analysis showed that the proportion of the CD122high Sca-1high subpopulation in the BM increased by ∼5-fold compared with that in the SP (Fig. 3B). Consistently, the number of TSCMs grew significantly when compared with that in the SP (Fig. 3C). As previously reported, CD8+ TSCMs could be generated by activating CD8+ T cells in vivo, when coupled with pharmacological activation of Wnt signaling.2 To mimic physiological conditions, a relatively low dose of TWS119 was injected intraperitoneally into mice whose T cells were activated by OVA injection to facilitate the minimum generation of TSCMs in vivo (Fig. S7, Supplemental Digital Content 1, http://links.lww.com/JIT/A529).2 The ratios and numbers of CD122highSca-1high TSCMs significantly increased in both BM and SP upon TWS119 treatment (Fig. 3D). In particular, the number and ratio of TSCMs in the BM was 4- to 5-fold higher than that in the SP (Figs. 3D, E, Fig. S2, Supplemental Digital Content 1, http://links.lww.com/JIT/A529). In addition, the expression of Bcl-2 was upregulated in BM-resident TSCMs compared with that in their SP-derived counterparts or freshly isolated SP-derived naive T cells (Fig. 3F). Taken together, these results demonstrate that the CD122high Sca-1high TSCMs preferentially homed to the BM.
P-Selectin or E-Selectin/P-Selectin Glycoprotein 1 (PSGL-1) and Vascular Cell Adhesion Protein 1 (VCAM-1) Mediate the Homing of TSCMs to the BM
The translocation of CD8+ TCMs and HSCs to BM microvessels is dependent on the interactions between adhesion molecules such as VLA-4/VCAM-1 (CD106), P-selectin and E-selectin/PSGL-1, or CXCL-12/CXCR4.18,25,44,45 Given the similar homing properties of TSCMs, TCMs, and HSCs, studies of the homing of TCMs and HSCs may help to elucidate the mechanism underlying the homing of TSCMs. To verify this hypothesis, the expression of candidate adhesion molecules in BM and SP was determined by flow cytometry. The results showed that adhesion molecules, including LFA-1, CXCR4, integrin α4β7, and PSGL-1, were involved in T-cell homing and did not exhibit significant differences in expression (Fig. 4A, Fig. S8, Supplemental Digital Content 1, http://links.lww.com/JIT/A529).18,46,47 Of note, integrin-α2, a key mediator of the homing of CD4+ memory T cells to the BM, was detected at a low level on the surface of TSCMs (Fig. 4A, Fig. S8, Supplemental Digital Content 1, http://links.lww.com/JIT/A529).20 P-selectin and E-selectin as well as VCAM-1 molecules are detected in the normal BM sinusoid. It is interesting to note that, the expression of VCAM-1 was moderately higher in BM-resident TSCMs than in naive T cells (Fig. 4A, Fig. S8, Supplemental Digital Content 1, http://links.lww.com/JIT/A529). To determine whether these adhesion molecules mediate the homing of TSCMs to the BM, we generated TSCMs cells with TWS119 in vitro and isolated TSCMs by flow cytometry. CD8+ TSCMs were labeled with CMTPX and then mixed with CFSE-labeling SP cells at ratio of 1:1. The mixed cells were injected into recipient mice, followed by the injection of corresponding antibodies intravenously 6 hours later. After 1 day, we examined the ratios of CMTPX-positive and CFSE-positive cells and calculated the HI. Compared with treatment with immunoglobulin G, flow cytometric analysis showed that the treatment with anti-VCAM-1, anti-P-selectin, anti-E-selectin, or anti-PSGL-1 antibodies significantly downregulated the homing of TSCMs into the BM (Figs. 4B, C). In addition, treatment with anti-CXCL-12 did not result in significant differences in the homing of TSCMs into all the organs (Figs. 4B, C). Together, these data indicate that P-selectin, E-selectin, PSGL-1, and VCAM-1 are the key mediators of the homing of TSCMs.
BM-resident TSCMs Have Enhanced Antitumor Activity Relative to SP-resident TSCMs in Response to Tumor-Antigen Challenge
Tumor-specific cytotoxic T cells or chimeric antigen receptor T cells are currently applied clinically for targeted cancer therapy. The B16 murine melanoma model is useful for the study of malignant melanoma in humans.31 In order to perform OVA-specific OT-Imice for studying TSCM specificity against tumor antigens, we constructed the B16-OVA cell line as previously described. We hypothesized that the microenvironment of the BM enables the generation of TSCMs with higher antitumor activity; accordingly, we generated OVA-specific CD8+ TSCMs in vivo via injection of TWS119 and tested the antitumor activities. As expected, the BM-derived TSCMs possessed higher antitumor reactivity than the SP-derived TSCMs in the adoptive transfer experiment (Fig. 5A). Furthermore, the transfer of BM-derived TSCMs significantly extended the survival of mice compared with that achieved following the transfer of SP-derived TSCMs (Fig. 5B). Thus, the results suggest that the adoptively transferred BM-derived TSCMs exhibited enhanced antitumor activity and higher therapeutic efficacy than conventional SP-derived TSCMs in mice.
In this study, CD8+ TSCMs that highly expressed CD122, Sca-1, Bcl-2, and CXCR3 were identified within the BM-resident naive-like T-cell compartments. Although a small number of natural TSCMs were detected in the peripheral lymphoid organs, including in the SP, PB, or LN, the ratios of natural TSCMs in these organs were much lower than those in the BM. Notably, similar to SP-derived TSCMs, the BM-resident TSCMs were capable of acquiring effector functions more rapidly upon blood-borne antigen exposure than naive T cells. These data also suggest that TSCMs significantly accumulated in the BM, rather than being simply confined to peripheral inflammatory sites. Nevertheless, the differences in species (mouse and nonhuman primates) resulted in differences in the distribution of CD8+ T-cell subsets in lymphoid organs, which was manifested in the distribution of CD8+ TCMs (larger numbers of mouse CD8+ TCMs in BM, in contrast with larger numbers of rhesus CD8+ TCMs in the LNs).9 Further, the distribution of CD8+ TSCMs in mice was different from that in nonhuman primates. Therefore, the natural distribution of CD8+ TSCMs in the human body requires further in-depth study. In addition, our data provided novel insights into the cytotoxic activity of TSCMs in the BM, whose function has thus far been ambiguous, and suggested a possible mechanism for the enhanced antitumor activity of BM T cells.
Despite the concomitant expression of numerous markers of naive T cells on the surface of TSCMs, both bioinformatics analysis of microarray data and antigenic stimulation experiments have suggested that TSCMs are most closely related to TCMs.3 However, it remains unknown whether the other characteristics of TSCMs, especially the trafficking properties, are similar to those of TCMs. The BM plays an important role in controlling immune responses by influencing the generation of lymphocytes and the maintenance of immunologic memory.16 Through investigations of the homing and retention of TSCMs in the BM, we found that both in vivo-generated and in vitro-generated TSCMs preferentially relocated to the BM (Fig. 3). Unfortunately, the results of the homing assay with CD8+ TSCMs generated by Wnt3A protein in vitro were not absolutely consistent with the results of in vivo studies. We speculated that introduction in vitro may be more efficient. Therefore, the homing efficacy of in vivo-generated TSCMs was higher than that of in vitro-generated TSCMs. Although TSCMs could be induced from naive T cells in vivo and were detected in the BM, the anatomic sites of transition from the naive state have not yet been determined.
The process of the accumulation of leukocytes in tissue depends on a series of adhesive interactions with vessels that involve tethering, rolling, or sticking. Although each adhesion procedure is mediated by several specific receptor-ligand pairs, each leukocyte possesses its own indispensable, subset-specific set of traffic molecules. We have demonstrated that the homing of TSCMs to the BM is dependent on adhesive interactions between TSCMs and BM vessels. Furthermore, the blocking experiment with certain antibodies resulted in a dramatic decline of BM-resident TSCMs in vivo, whereas the CD8+ TSCMs were arrested in the SP. CD8+ TSCMs, as a long-term subset, would be relocated to the immune organs in favor of their own self-renewal. SP, as the largest peripheral lymphoid organ, is one of the main locations at which the CD8+ TSCMs are arrested. Therefore, the migration of CD8+ TSCMs to the SP is indispensable when their migration to the BM is blocked. This phenomenon suggests that all 4 adhesion molecules analyzed in our study, namely P-selectin, E-selectin, PSGL-1, and VCAM-1, act as mediators for the homing of TSCMs into the BM. A significant decline of TSCMs in the SP was observed after injection of anti-PSGL-1. Of note, P-selectin and E-selectin as well as VCAM-1 are enriched in BM microvessels, whereas PSGL-1, the ligand of P-selectin and E-selectin, is expressed on most immune cells and facilitates the homing of resting T cells into lymphoid organs.48 Therefore, the mechanism underlying the presence of TSCMs in the BM involves adhesive interactions between PSGL-1 and P-selectin or E-selectin, whereas TSCMs appear to home to the SP in a PSGL-1-independent manner. In particular, VCAM-1, the adhesion protein expressed in TSCMs and microvessels, was found to be crucial for the homing of TSCMs into the BM rather than into the SP; however, we have not yet identified the specific tissue-resident molecules that predominate in this process. The administration of various neutralizing antibodies altered the BM microenvironment surrounding the BM-resident CD8+ TSCMs and blocked the homing of CD8+ TSCMs into the BM. Under such conditions, the adoptively transferred CD8+ TSCMs were retained in the PB. Our data elucidate the specific migratory routes of TSCMs to the BM. Nevertheless, there may be additional unidentified factors involved in this process. The induction of adhesion-related molecules appears to be a critical step in the development of a stable TSCM compartment in the BM; however, the underlying mechanism merits further investigation. In contrast to previous reports describing the relocation of CD8+ TCMs in BM, the homing of CD8+ TSCMs did not seem to be dependent on CXCL-12.18 In a previous study, the dependence of memory T-cell homing to the BM on CXCL12 was strongly implicated, with reduced integrin activation after anti-CXCL12 treatment.18 We attempted to confirm the changes of integrin activation in CD8+ TSCMs; however, no differences were observed, at least in integrin-α4β7, integrin-α2, and integrin-β1 protein. It was speculated that the CD8+ TSCM subset is different from CD8+ TCM subset at this point, as they are 2 different subsets.
An appropriate microenvironment for BM-resident TSCMs requires conditions that facilitate the homeostasis of TSCMs in specific areas. In particular, the microenvironment in the BM provides not only a homeostatic proliferation signal but also a survival signal by upregulating the expression of Bcl-2 for the maintenance of TSCMs. The cellular DNA content, which was determined by detection using propidium iodide (PI), indicated that BM-resident TSCMs were in a resting status and represented a certain degree of stem cell characteristics; however, the expression of CD69 in BM-resident TSCMs was slightly higher than that in naive T cells. Simultaneously, BM-resident TSCMs could be reactivated rapidly upon exogenous antigen invasion, which suggests that active TSCMs are more likely to reside in areas close to APCs. We speculate that antigen-specific responses may be accompanied by the confluence of TSCMs into large aggregates with several APCs, leading to the activation of TSCMs in the BM. Given that a minority of TSCMs was found in the peripheral immune organs and a large number of TSCMs accumulated in inflammatory sites rapidly, we proposed that these cells utilized the niches in the BM as a refuge, and could be temporarily hidden from antigenic exposure before executing immunologic surveillance.
Our data indicate that the BM-resident TSCMs exert much stronger antitumor activity, which may be instructive for development of tumor immunotherapy. In melanoma patients, high frequencies of tumor-specific T cells were detected. However, most of these cells were anergic or nonresponsive.49,50 Compared with other subsets, TSCMs show higher antitumor activity. Although the expression of IFN-γ and cell proliferation of natural SP-derived TSCMs was almost equal to those of natural BM-derived TSCMs, we exploited the fact that the microenvironment in the BM could generate more functional and tumor-specific TSCMs in vivo. In addition, we demonstrated that the in vivo-generated TSCMs derived from the BM could significantly extend the survival of mice compared with SP-derived TSCMs. Therefore, the present work showed that the BM microenvironment was more conductive to the induction of functional CD8+ TSCMs; however, the underlying mechanisms remain unknown and need further study. Of note, in the present work, approximately half of the mice with BM TSCMs died, although the tumors were still small. We speculate that tumor metastasis occurs in the B16 model, despite subcutaneous injection as previously described.51 Therefore, tumor migration may lead to the death of mice in the B16 model, even when the tumor size is not very large.2 Our data suggest that the selection of an appropriate microenvironment for tumor-specific TSCMs represents a novel strategy to improve the efficacy of anti-tumor immunotherapies.
Overall, our study has demonstrated that TSCMs, a distinct memory cell subset, exist naturally in WT mice and principally accumulate in the BM. In addition, the present findings show that PSGL-1 interacted with P-selectin and E-selectin to mediate the homing of TSCMs to the BM. In addition, VCAM-1 appears to be involved in this process. Moreover, these findings should contribute to the development of effective antitumor immunotherapy strategies by potentially enabling the production of tumor-antigen–specific TSCMs for patients with cancer.
MATERIALS AND METHODS
OT-I, C57BL/6J, and CD45.1 (B6.SJL-PtprcaPep3b/BoyJ) mice were purchased from Jackson Laboratories and bred under specific pathogen-free conditions at Sun Yat-Sen University. All experiments performed on mice were approved by the Institutional Animal Care and Use Committee of Sun Yat-Sen University.
Flow Cytometry and Sorting
Single-cell suspensions were prepared from SP, mesenteric LN, blood, or BM of individual mice. For cell staining, cells were preincubated in 0.1% bovine serum albumin/phosphate-buffered saline solution of 10 μg/mL anti-FcgRII/III (2.4G2) (BD Pharmingen, San Jose, CA) for 10 minutes at 4°C. The cells were then stained for 20 minutes at 4°C with primary antibodies. For cell sorting, BD FACS AriaII cell sorter (BD Biosciences, San Jose, CA) was used. For intracellular cytokine staining, cells were stimulated with phorbol 12-myristate 13-acetate (100 ng/mL; Sigma-Aldrich, St. Louis, MO) and ionomycin (1 μg/mL; Sigma-Aldrich) in the presence of 5 μg/mL brefeldin A (Sigma-Aldrich) for 4 hours. Cells were washed twice in phosphate-buffered saline, and then fixed and permeabilized with BD Cytofix/Cytoperm Fixation/Permeabilization Kit. Stained samples were analyzed in BD LSR II Fortessa (BD Biosciences). Flow cytometric data were analyzed with FlowJo (Tree Star) software.
Primary antibodies used in the study include anti-CD62L (MEL-14) (eBiosciences, San Diego, CA), anti-CD45.2 (104) (eBiosciences), anti-CD44 (IM7) (eBiosciences), anti-CD3 (145-2C11) (eBiosciences), anti-Sca-1 (D7) (BD Pharmingen), anti-CD8 (53-6.7) (eBiosciences), anti-TCRβ (H57-597) (eBiosciences), anti-LFA-1 (H155-78) (eBiosciences), anti-IFN-γ (XMG1.2) (eBiosciences), anti-CD4 (RM4-5) (eBiosciences), anti-5-bromo-2'-deoxyuridine (BrdU) (3D4) (eBiosciences), anti-CD69 (H1.2F3) (eBiosciences), anti-CD127 (A7R34) (eBiosciences), anti-CXCR4 (2B11) (eBiosciences), anti-VCAM-1 (429) (eBiosciences), anti-CD62P (RB40.34) (BD Pharmingen), anti-CD29 (eBioHMb1-1) (BD Pharmingen), anti-CD183 (CXCR3-173) (BD Pharmingen), anti-Bcl-2 (3F11) (BD Pharmingen), anti-integrin-α4β7 (DATK32), anti-CD162 (2PH1) (eBiosciences), and anti-CD62E (P2H3) (eBiosciences).
Total RNA was isolated with TRIzol reagent (Life Technologies) and then subjected to complementary DNA (cDNA) synthesis with PrimeScript reverse transcription (RT) reagent kit (TaKaRa, Shiga, Japan). All primers were annealed at 37°C and RT was performed at 42°C. Quantitative PCR was performed with SYBR premix Ex Taq II kit (TaKaRa) following the manufacturer’s instructions. Sequences of primers are listed in Supplemental Table I (Supplemental Digital Content 1, http://links.lww.com/JIT/A529).
Generation of TSCM Cells In Vivo and In Vitro
The CD44lowCD62Lhigh cells were stimulated with 2 μg/mL anti-CD3 (BD Pharmingen), 1 μg/mL anti-CD28 (BD Pharmingen), and 10 ng/mL IL-2 (Peprotech, Rocky Hill, NJ) in the presence of TWS119 (7 μM) (Selleckchem, Houston, TX) or Wnt3A protein (1 μg/mL) (Peprotech) in vitro. For generation of TSCMs in vivo, 2×106 OT-I naive CD8+ T cells were adoptively transferred into congenic CD45.1 mice and then injected intraperitoneally (500 μg) per mouse OVA (Sigma-Aldrich) with complete Freund’s adjuvant (CFA) (Sigma). Mice received 4 doses per day of TWS119 at 40 mg/kg from day 0 to day 3. Six days after injection, mice with or without the treatment of TWS119 were sacrificed for further analysis. The CD8+ TSCMs were isolated by flow cytometry on the basis of the expression of surface markers (CD3+ CD4− CD8+ CD62L+ CD44− CD122+ Sca-1+ T cells for in vitro-generated TSCMs or CD45.1+ CD8+ CD62L+ CD44−CD122+ Sca-1+ T cells for in vivo-generated TSCMs).
In Vivo Activation of CD8+ T Cells
Cells of 3 T-cell subsets [5×105; naive T cells: CD3+ CD8+ CD62L+ CD44− Sca-1− CD122−; central memory T cells (TCMs): CD3+ CD8+ CD62L+ CD44+; TSCMs: CD3+ CD8+ CD62L+ CD44− Sca-1+ CD122+] from SP or BM of OT-Imice were adoptively transferred to CD45.1 mice. Recipients were immunized with 500 μg of OVA in CFA and sacrificed after 3 days for further analysis.
Cell proliferation in vitro was determined by BrdU staining. CD44low CD62Lhigh T cells (at a concentration of 2×106/mL from SP or BM were cultured in RPMI 1640 medium (Gibco, Carlsbad, CA) containing 9% fetal bovine serum (Gibco, Carlsbad, CA), penicillin (100 U/mL) (Hyclone; GE Healthcare Life Sciences, Chicago, IL), and streptomycin (100 μg/mL) (Hyclone; GE Healthcare Life Sciences). For the activation of C57BL/6J mice-derived T cells, cells were stimulated with anti-CD3 (2 μg/mL) and anti-CD28 (1 μg/mL) (BD Pharmingen) in the presence of IL-2 (10 ng/mL) (Peprotech). For the activation of OT-Imice-derived T cells, experiments were performed in accordance with previously described protocols.52 Briefly, 1×106/mL T cells were cocultured with 2×107/mL irradiated T-depleted SP or BM-derived antigen-presenting cells in the presence of OVA257–264 peptides (SIINFEKL) (2 μM) (Anaspec, San Jose, CA) and IL-2 (10 ng/mL) (Peprotech).
For in vitro labeling with BrdU, cells were stimulated and then incubated with BrdU at a final concentration of 10 µM in cell culture medium before being harvested at 16 hours. For the in vivo proliferation assay, BrdU was diluted at a concentration of 10 mg/mL as a stock solution; then, 200 µL of the stock solution was injected into each mouse.
Homing experiments of CMTPX-labeled TWS119-induced or vehicle-treated control cells and CFSE-labeled reference cells were performed as described previously, with some modifications.53 Briefly, 2×106 CMTPX-labeled (10 μM) TWS119-induced CD8+ TSCMs or vehicle-treated control cells (or SP naive T cells) were mixed with the same number of newly isolated and CFSE-labeled (10 μM) SP cells and then injected intravenously into the CD45.1 recipients. The recipients were sacrificed after 24 hours, and cells from SP and BM were obtained as described to measure CMTPX+/CFSE+ ratios by flow cytometry. The input ratio (IR=[CMTPX]input/[CFSE]input) was assessed using an aliquot. HI was calculated as the ratio of [CMTPX]tissue/[CFSE]tissue to [CMTPX]input/[CFSE]input. For instance, a HI of 1 indicates that the frequency of CMTPX-staining cells was equivalent to that of naive cells labeled with CFSE.
B16 Murine Model
B16 cells were kindly provided by Professor Jie Zhou and B16-OVA cells were established as described.31,54 Briefly, we extracted OVA mRNA from hen oviduct and obtained cDNA by RT. OVA-expressing plasmid was constructed by inserting the OVA cDNA into retroviral vector plasmid pMSCV-puro (Clontech Laboratories Inc.) to generate plasmid pMSCV-OVA. pMSCV-OVA was cotransfected with the pIK packaging plasmid into 293T cells using the calcium phosphate transfection method. Forty-eight hours after transfection, supernatants were collected and incubated with B16 cells. The transfected cells were incubated for 24 hours in the presence of polybrene (2.5 μg/mL; Sigma-Aldrich). Puromycin (4 μg/mL; Sigma-Aldrich) was then used to select the stably transfected cells over a 12-day period. Next, C57BL/6J mice were injected intradermally with 1.5×106 B16-OVA cells. After 10 days, 5×104 OVA-specific TSCMs, which were isolated from SP or BM of CD45.1 recipient mice after injection of OVA (0.5 mg per mouse) with CFA and TWS119 (40 mg/kg), were adoptively transferred into the tumor-bearing WT mice. The tumor burden was measured by testing tumor size and survival rates.
CONFLICTS OF INTEREST/FINANCIAL DISCLOSURES
Supported by the National Special Research Program of China for Important Infectious Diseases (2018ZX10302103, 2017ZX10202102-003, and 2018ZX10101004003001), the Important Key Program of Natural Science Foundation of China (81730060), the International Collaboration Program of Natural Science Foundation of China and US NIH (81561128007), the Joint-innovation Program in Healthcare for Special Scientific Research Projects of Guangzhou (201803040002), the National Science and Technology Major Project (2018ZX10101004003001), and the National Natural Science Foundation of China (81601759).
All authors have declared that there are no financial conflicts of interest with regard to this work.
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