Negative selection is the process by which the developing lymphocyte receptor repertoire rids itself of autoreactive specificities. One mechanism of negative selection in developing T cells is the induction of apoptosis in immature CD4+CD8+ (DP) thymocytes, referred to as clonal deletion. Clonal deletion is necessarily T cell receptor (TCR) specific, but TCR signals alone are not lethal to purified DP thymocytes. Here, we identify two distinct mechanisms by which TCR-specific death of DP thymocytes can be induced. One mechanism requires simultaneous TCR and costimulatory signals initiated by CD28. The other mechanism is initiated by TCR signals in the absence of simultaneous costimulatory signals and is mediated by subsequent interaction with antigen-presenting cells. We propose that these mechanisms represent two distinct clonal deletion strategies that are differentially implemented during development depending on whether immature thymocytes encounter antigen in the thymic cortex or thymic medulla.
Acentral feature of the immune system is its ability to respond to foreign antigens while tolerating self-antigens. Burnet's model of self-nonself discrimination proposed that receptor engagements that were stimulatory for mature immune cells would induce immature immune cells to die, resulting in the removal of autoreactive receptor specificities from the developing repertoire (1–2). The removal of autoreactivities from the functional lymphocyte repertoire is known as negative selection. For T cells, negative selection can occur at different developmental stages in the thymus by a variety of mechanisms, including (a) clonal deletion, (b) developmental or clonal arrest, or (c) clonal inactivation or anergy (3–4). CD4+CD8+ double positive (DP)1 thymocytes in particular are susceptible to clonal deletion induced in response to TCR signals (5–7). Curiously, while clonal deletion of DP thymocytes must involve TCR engagement, TCR engagement by itself is insufficient to stimulate DP thymocyte apoptosis in vitro (8–12). Rather, DP thymocyte death has been found to require signals in addition to TCR, such as those provided by CD28 (9–11). This requirement for second signals parallels the requirement for second signals in TCR-mediated activation and proliferation of mature single positive (SP) T cells (13). Because CD28 is not a unique costimulatory molecule for mature T cells (14–22), it is likely that CD28 is not the only molecule capable of transducing second signals for TCR dependent DP thymocyte apoptosis (6, 14, 23–24). Indeed, other molecules have been implicated in clonal deletion of DP thymocytes, such as CD30 (21) and fas (25). The role of fas in negative selection is particularly controversial (26–29).
TCR-dependent apoptosis of mature T lymphocytes was not foreseen in Burnet's model of self-nonself discrimination but is now a recognized consequence of mature T cell activation (reviewed by 30–31). In mature T cells, TCR signals do not directly induce an apoptotic program, but rather act indirectly by upregulating surface expression of members of the TNF family, specifically fas ligand (fasL) and TNF (32–34). These proteins bind to fas or TNF receptor (TNFR) which mediate apoptosis through death domains expressed in their cytosolic regions (35). This mechanism of apoptosis necessarily results in death of both TCR-stimulated T cells and neighboring (or bystander) cells expressing fas or TNFR. In contrast, clonal deletion in the thymus is presumed not to involve bystander death since it should be limited to cells directly stimulated by TCR interactions.
In this study we have focused on identifying mechanisms of TCR-dependent clonal deletion of rigorously purified DP thymocytes to avoid confounding signals that can result from contact with other thymic elements. We identify two distinct mechanisms for generating second signals leading to TCR-induced DP thymocyte apoptosis: (a) a CD28-dependent mechanism that requires simultaneous engagement of TCR and CD28 surface molecules, and (b) a CD28-independent mechanism initiated by TCR signals but mediated subsequently by APC signals. While we found that fas signals can induce DP thymocyte death, they were not involved in either TCR-specific apoptotic mechanism. We propose that the two mechanisms of DP apoptosis revealed in this report represent two distinct TCR-specific clonal deletion strategies in the thymus: (a) a CD28-dependent mechanism specific for antigens on B7+ cells, i.e., APC and medullary epithelium, and (b) a CD28-independent mechanism specific for antigens on B7− cells in the thymic cortex.
Materials And Methods
Young adult female C57BL/6 (B6) mice, gld/gld mice (B6-SMN C3H fasL), and lpr/lpr mice (B6 mrl lpr/lpr) were obtained from The Jackson Laboratory (Bar Harbor, ME) and young adult female B6 Ly5.2 mice were obtained from the Frederick Cancer Research Center (Frederick, MD). CD28-deficient mice (CD28 KO) (14) were bred to the C57BL/6 background and maintained at the Bethesda Naval Medical Research Institute. Mice transgenic for the human bcl-2 gene (driven by the lck proximal promoter  were generously provided by Dr. Stanley Korsmeyer and bred in our facility at the NIH. Mice deficient in either the p55 TNFR (p55) (37) or both p55 and p75 TNFR (38 and 38a) were obtained from Immunex (Seattle, WA).
CD4+CD8+ thymocytes were purified from 4–6-wk-old female mice either by panning on anti-CD8 (83-12-5) coated plates (39) or by Percoll density fractionation (40). Similar experimental results were obtained with cells isolated by either procedure. In each case >95% of isolated cells were CD4+CD8+. APC were prepared by treating splenocytes with anti-CD4 (RL-172), anti-CD8 (3-155), anti-Thy-1 (30H12), and rabbit complement as previously described (3). Viable cells were isolated by centrifugation over Lymphocyte-M (Cedarlane Laboratory, Ltd., Ontario, CA). These cell preparations were free of T cells as determined by CD3 staining and FACS® analysis. Lymph node T cells were prepared from B6 and gld/gld mice by treating single-cell suspensions of cells isolated from a pool of popliteal, inguinal, axillary, brachial, and submandibular lymph nodes with a combination of anti-class II (M5114), anti-NK1.1 (PK136), anti-HSA (J11d) culture supernatants, and rabbit complement.
Anti-CD28 (37.51 ) and anti–TCR-β (H57-597 ) were affinity purified in our laboratory from hybridoma culture supernatant on columns of protein G– and protein A–Sepharose (Pharmacia LKB Nuclear, Gaithersburg, MD), respectively. Anti-CD2 (RM2-5), anti-CD43 (S7), anti-CD27 (LG.3A10), anti-41BB (1AH2), neutralizing anti–TNF-α (G281-2626), anti-CD80 (1G10), anti-FcR (2.4G2), anti-fas (Jo2), and FITC-conjugated anti-HSA, FITC anti-Ly5.2 (CD45.1) and FITC anti-Ly5.1 (CD45.2) were purchased from Pharmingen laboratories. FITC-conjugated anti-CD5 (Ly-1) was purchased from Beckton Dickinson (San Jose, CA). Anti-CD81 was the product of hybridoma 2F7 (43). Anti-CD9 (9D3 ), anti-CD24 (20C9 ), anti-CD30 (mCD30.1 ), anti-CD30L (M15 ), and anti-B7-2 (GL1 ), were generously provided by Drs. Hiromi Fujiwara (Osaka University, Osaka, Japan), Charles Janeway (VCI, NIH, Bethesda, MD), Eckhardt Podack (University of Miami School of Medicine, FL), Phil Morrissey (Immunex, Seattle, WA), and Richard Hodes (NIH, Bethesda, MD), respectively.
Murine recombinant TNF-α (R&D Labs., Minneapolis, MN) was used at a final concentration of 100 ng/ml. CD30-Ig was generously provided by Dr. Eckhardt Podack. Cyclosporine A was purchased from Calbiochem-Novabiochem (La Jolla, CA) and cycloheximide, wortmannin, and GF109203X were purchased from Sigma Chem. Co. (St. Louis, MO). The caspase inhibitor Cbz-Val-Ala-Asp-(Ome)-fluoromethyl ketone (ZVAD-FMK) was purchased from Enzyme Systems Products (Dublin, CA).
Culture and Stimulation Conditions.
Purified cell populations were cultured for 16–20 h in a 7% CO2 humidified incubator in RPMI 1640 supplemented with 5 × 10−5 M 2-ME and 10% FCS at 37°C. Single-cell suspensions of DP thymocytes were plated in 24-well tissue culture plates (Corning Glass, Corning, NY) at a cell density of 2 × 106/ml in a total of 500 μl per well. When mixed culture experiments were performed, DP cells from CD28-deficient mice were incubated with DP cells from Ly5.2 mice at a 1:1 ratio and with LN T from Ly5.2 mice at a 1:2 or 1:3 ratio. APC were mixed with DP thymocytes at a 2:1 or 3:1 ratio and 3 × 106 total cells were plated per well. For stimulation, wells in a 24-well plate were coated with antibody combinations by incubating them overnight at 4°C with 350 μl of a 10 μg/ml (most antibodies) or 50 μg/ml (anti-CD28) of each affinity-purified antibody specified in PBS.
Staining and Flow Cytometry.
Cell death was assayed as previously described (9, 48). In brief, 5 × 105 cultured cells were incubated with saturating concentrations of the FITC conjugated antibodies specified in staining medium (HBSS, 0.5% BSA, 0.5% NaN3) for 30 min at 4°C, washed, and then incubated with a 1 μg/ml ethidium bromide (EtBr; Sigma) for another 30 minutes at 4°C. Cells were washed again and analyzed using CellQuest software on a FACScan®. In mixed cell culture experiments, DP thymocytes were identified by expression of Ly5.1, Ly5.2, HSA, and Thy-1, as indicated.
Measures of Cell Death.
Specific cell death (% cell death) was determined by EtBr staining and was calculated as a normalized value as follows: (%EtBr+ (stimulated) − %EtBr+ (unstimulated control))/(100 − %EtBr+ control). Background EtBr staining of cultured DP thymocytes ranged between 18 and 30%. To compare thymocyte apoptosis in response to TCR-CD28 signals among experimental groups with different internal controls (i.e., different mouse strains, different solvents, etc.), individual responses were normalized and expressed as a killing index. The killing index was calculated as follows: (% DP cell death induced by TCR-CD28 under experimental conditions)/(% DP cell death induced by TCR-CD28 under control conditions). Killing index = 1.0 means that the indicated condition did not affect TCR-CD28– induced apoptosis; killing index >1 means that the indicated condition inhibited TCR-CD28–mediated death. All experiments displayed were performed three or more times with similar results.
Surface Molecules Expressed by CD4+CD8+ Thymocytes That Kill Cells by Either TCR-dependent or TCR-independent Mechanisms.
To identify the molecular requirements for TCR-dependent DP thymocyte apoptosis, we stimulated purified DP thymocytes in vitro and assessed them for EtBr uptake, which identifies cells undergoing apoptosis (9, 48). We initially examined surface molecules for their ability to induce apoptosis of DP thymocytes in the absence of TCR engagement (Fig. 1,a). In fact, we identified two stimuli that induced DP thymocyte apoptosis in a TCR-independent manner, namely (a) fas engagement by immobilized platebound antibody and (b) TNFα engagement of TNFR. Antibody engagement of surface fas molecules induced apoptosis of most DP thymocytes, consistent with others' observations and the high expression of fas on DP thymocytes (49); and soluble TNF-α engagement of surface receptors induced apoptosis of 20% of DP thymocytes, which may represent a distinct TNF-α responsive subpopulation (50) (Fig. 1 a). Our present finding that immobilized anti-fas antibody efficiently induces DP thymocyte death differs from that of Ogasawara et al. (51) who found that metabolic inhibitors were necessary to enhance DP thymocyte death induced by soluble anti-fas antibodies. We think that our different observations may be due to differences in the efficiency by which fas is crosslinked by soluble versus immobilized antibody.
Even though fas and TNFR are members of the TNFR family of proteins (52), many of which induce cell death, platebound antibody engagement of three other members of the family (CD27, CD30, and 41BB) did not affect DP thymocyte viability (Fig. 1,a, right). In fact, no other molecules examined, including platebound antibodies specific for CD4, CD5, CD8, CD69, and LFA-1 (9 and data not shown), were capable of mediating TCR-independent DP thymocyte apoptosis (Fig. 1 a).
We next assessed molecules that could induce DP thymocyte apoptosis in the presence of TCR engagement (Fig. 1,b). As expected (9), TCR engagement alone failed to induce significant DP thymocyte apoptosis (Fig. 1,b). We examined three specific sets of surface proteins for their ability to cooperate with the TCR to kill DP thymocytes (Fig. 1,b and data not shown), namely (a) molecules thought to be costimulatory (CD9 ), CD28 [reviewed in 53], CD43 , and CD81 , (b) coactivating molecules that enhance TCR signaling (CD2, CD4, CD5, CD8, CD24, CD69, and LFA-1), and (c) selected TNFR family members (CD27, CD30, 41BB), which may also exhibit costimulatory activity (15, 17–18, 21–22, 52). Importantly, antibody engagement of each of these molecules cooperated with TCR signaling to upregulate CD5 expression on DP thymocytes (data not shown). However, only CD28 cooperated with TCR to induce DP thymocyte apoptosis (Fig. 1 b).
Thus, there exist both TCR-independent and TCR-dependent mechanisms of DP thymocyte apoptosis: TCR-independent mechanisms can be mediated by either fas or TNFR engagement, whereas the TCR-dependent mechanisms can be mediated by coengagement of TCR and CD28.
TCR/CD28–induced Apoptosis Is Independent of fas and TNFR Interactions, and Is Strictly Confined to DP Thymocytes That Have Received both TCR and CD28 Signals.
The ability of fas and TNF-α to mediate DP thymocyte apoptosis raised the possibility that both mechanisms of DP thymocyte apoptosis (TCR-independent and TCR-dependent) may ultimately result from engagement of fas or TNFR. To address this possibility, we examined the ability of TCR-CD28 coengagement to kill purified DP thymocytes from mice deficient in (a) fas (lpr, reviewed in reference 55), (b) fas ligand (gld), (c) the p55 murine TNFR, or (d) both the p55 and p75 murine TNFRs (38, 38a) (Fig. 2). None of the mutations significantly affected the ability of TCR-CD28 coengagement to induce apoptosis of DP thymocytes, indicating that neither fas nor the TNF receptors p55 or p75 were required (Fig. 2). In addition, neutralizing anti–TNF-α antibodies had no effect on TCR-CD28– induced apoptosis of wild-type DP thymocytes (data not shown). We also found that TCR-CD28–induced death was not blocked by CD30 Ig, a fusion protein that blocks CD30-CD30L interactions (data not shown). We conclude that TCR-CD28 coengagement induces DP thymocyte apoptosis by a mechanism that is independent of fas/fasL, TNF-TNFR, and CD30-CD30L interactions.
While fas and TNFR are not involved in TCR-CD28– induced apoptosis, additional members of the TNFR family expressing the “death domain” associated with apoptotic signaling continue to be identified (56–58). To determine if TCR-CD28 coengagement induced apoptosis in trans of bystander thymocytes via ligands (known and unknown), we used thymocytes from CD28 KO mice as bystander cells for they do not die in response to TCR-CD28 stimulation (Fig. 3,a). In this mixed culture experiment, we stimulated cocultures of DP thymocytes from wild-type (B6-Ly5.2) and CD28 KO mice with both anti-TCR and anti-CD28 platebound antibodies (Fig. 3,b). We found that the majority of wild-type DP thymocytes died in cocultures in response to TCR-CD28 coengagement. In contrast, bystander CD28 KO DP thymocytes did not die even though they were present in the same cocultures and even though they were stimulated by the immobilized anti-TCR antibodies (Fig. 3,c). These results demonstrate that TCR-CD28 coengagement only induces death of DP thymocytes that had been stimulated by both TCR and CD28 signals, and suggests one of two scenarios as illustrated in Fig. 3 d. Either TCR-CD28 transduces intracellular signals that directly activate an intrinsic death program in DP thymocytes, or TCR-CD28 coengagement stimulates surface expression of an unknown death domain bearing molecule that signals cell death upon interaction with its ligand which must also be expressed on DP thymocytes. In the latter case, the death receptor-ligand interaction could conceivably operate either on an individual DP thymocyte (i.e., cis) or between interacting DP thymocytes (trans).
Identification of Apoptotic Signals Generated by TCR/CD28 Stimulation.
To characterize the molecular basis for TCR-CD28–induced apoptosis of DP thymocytes, we assessed specific inhibitors for their ability to abrograte DP thymocyte death (Fig. 4). We found that neither cyclosporine A (reviewed in reference 59) nor wortmannin (60, 61) inhibited TCR-CD28–mediated death (Fig. 4), indicating that calcineurin and PI 3-kinase activity are not required. In contrast, DP thymocyte apoptosis induced by TCR-CD28 coengagement was inhibited by (a) GF109203X, a specific inhibitor of protein kinase Cγ (PKCγ (61, 62), (b) the protein synthesis inhibitor, cycloheximide, and (c) the caspase (ICE-family protease) inhibitor, ZVAD-FMK (63, 64) (Fig. 4). Consistent with the participation of caspases, TCR-CD28 coengagement failed to induce significant apoptosis in DP thymocytes from bcl-2 transgenic mice which constitutively overexpress the anti-apoptotic bcl-2 protein (Fig. 4).
These data further suggest that the death mechanism initiated by TCR-CD28 coengagement is distinct from that initiated by fas engagement, for unlike TCR-CD28–mediated death, fas mediated death of thymocytes is not inhibitible by cycloheximide (65, 66) and may not be inhibitable by bcl-2 (67). To demonstrate this directly, we compared the effect of bcl-2 on DP thymocyte apoptosis induced by fas and TCR-CD28 engagement (Fig. 5). In this experiment, we cultured DP thymocytes from wild-type and bcl-2 transgenic mice with three different stimulators of apoptosis: dexamethasone, platebound antibodies against fas, and platebound antibodies against TCR-CD28. As expected, dexamethasone killed wild-type DP thymocytes but not DP thymocytes from bcl-2 transgenic mice (Fig. 5). More importantly, DP thymocytes that expressed bcl-2 were susceptible to fas mediated death but resistant TCR/CD28-induced death (Fig. 5). Thus, the death program initiated by TCR-CD28 coengagement is distinct from that initiated by fas engagement.
We conclude that apoptotic signals generated by TCR-CD28 coengagement are mediated by PKCγ, require protein synthesis, and result in the activation of intracellular caspases that are regulated by bcl-2.
Identification of a TCR-dependent but CD28-independent Mechanism of DP Thymocyte Apoptosis.
Our studies using an array of antibodies to known molecules on the surface of DP thymocytes did not identify any proteins other than CD28 that could cooperate with TCR to induce DP thymocyte apoptosis. To determine if any such molecule existed, we asked whether APC expressed ligands, known or unknown, for surface molecules that would cooperate with TCR to induce DP thymocyte apoptosis. In this coculture experiment, we stimulated DP thymocytes from wild-type and CD28 KO mice with platebound anti-TCR in the presence of APC. We confined our assessment of EtBr staining to DP thymocytes by excluding APCs from the analysis using an allelic marker, Ly5. DP thymocytes from wild-type mice died in response to TCR stimulation in the presence of APC. More importantly, DP thymocytes from CD28 KO mice also died in response to TCR stimulation in the presence of APC, indicating that APC possess ligands that engage molecules other than CD28 that can induce death of TCR-stimulated thymocytes. It is important to note that this CD28-independent mechanism of DP thymocyte death strictly requires engagement of TCR on DP thymocytes, as APCs did not kill unstimulated CD28 KO DP thymocytes (Fig. 6). From these data we can conclude that APC express or secrete ligands for surface molecules on DP thymocytes that are capable of cooperating with the TCR to induce TCR-dependent but CD28-independent apoptosis.
CD28-dependent and CD28-independent Mechanisms of TCR Induced DP Thymocyte Apoptosis Are Distinct.
The present results clearly indicate that CD28 is not the only surface molecule that the TCR can use to kill DP thymocytes. However, it is possible that even though CD28-dependent and CD28-independent mechanisms of TCR-induced DP thymocyte apoptosis are mediated by different surface receptor molecules on DP thymocytes, the second signals induced by these different proteins might be identical. That this is not the case was revealed by experiments in which TCR and second signals were induced sequentially rather than simultaneously. In this experiment, we prestimulated DP thymocytes with immobilized anti-TCR for 6 h and subsequently transferred them to cultures with platebound anti-CD28. We found that death of prestimulated DP thymocytes was not affected by subsequent stimulation through CD28 (Fig. 7,a). In fact, only subsequent coengagement of both TCR and CD28 together increased apoptosis of prestimulated DP thymocytes above background (Fig. 7,a). In contrast, we found in the same experiment that DP thymocytes from CD28 KO mice similarly prestimulated with immobilized anti-TCR and subsequently transferred to APCs were killed efficiently (Fig. 7,b). Thus, to stimulate DP thymocyte apoptosis, TCR and second signals induced by CD28 must be generated simultaneously, whereas TCR and second signals induced by APC can be generated sequentially, as illustrated in Fig. 7 c. Consequently, CD28-dependent and CD28-independent pathways of cell death represent two distinct mechanisms by which TCR can induce DP thymocyte apoptosis.
Characterization of TCR-dependent but CD28-independent Mechanisms of DP Thymocyte Apoptosis.
To determine if fas/ fasL interactions were involved in APC-induced cell death, we prestimulated CD28 KO DP thymocytes with platebound anti-TCR and then transferred them to cultures containing APCs isolated from fasL-deficient (gld) mice (Fig. 8). FasL-deficient APCs from gld mice mediated the death of TCR-stimulated DP thymocytes as efficiently, if not more efficiently, than wild-type APCs (Fig. 8). Thus, the CD28-independent mechanism of TCR-mediated DP cell death is also independent of fas/fasL interactions.
It was conceivable that the CD28-independent mechanism of cell death involved a CD28-like molecule such as CTLA-4 that could be engaged by B7 ligands on APC (68). In fact, this is not the case, as blocking antibodies to B7-1 and B7-2 failed to inhibit the ability of APCs to kill TCR-prestimulated DP thymocytes from CD28 KO mice (Fig. 8). Similar results were obtained with soluble CTLA-4 Ig (data not shown). Furthermore, the apoptosis observed was not a consequence of the transfer of small amounts of anti-TCR which could bind to Fc receptors (FcR) on APC, for the anti-FcR antibody 2.4G2 did not inhibit the apoptotic effects of sequential TCR and APC engagement (Fig. 8).
Finally, these data suggest that TCR prestimulation (in the absence of CD28 coengagement) “prepares” DP thymocytes to undergo apoptosis upon subsequent interaction with APC, possibly by inducing expression of surface molecules containing death domains that bind APC-derived ligands. Consistent with such a possibility, cycloheximide reduced by over 70% the number of TCR prestimulated DP thymocytes that died upon subsequent exposure to APC (data not shown), indicating that new protein synthesis is required to make TCR prestimulated DP thymocytes vulnerable to death. TNFR family members are attractive candidate molecules whose synthesis could be induced on DP thymocytes by TCR prestimulation. Indeed, CD30 has been reported to play a role in thymocyte negative selection (21). Nevertheless, CD30 does not appear to be involved as neither soluble CD30-Ig fusion protein (45) (Fig. 8) nor antibodies specific for the CD30 ligand (data not shown) blocked the ability of APCs to mediate CD28-independent apoptosis of prestimulated DP thymocytes.
The present report identifies two distinct mechanisms by which DP thymocytes can be induced to undergo apoptosis in response to TCR signals. In the CD28-dependent mechanism, TCR signals are delivered simultaneously with CD28 costimulatory signals, resulting in DP thymocyte death. In the CD28-independent mechanism, TCR signals are not accompanied by costimulatory signals and death signals are generated upon subsequent interaction with APCs. In addition the present study demonstrates that purified DP thymocytes can also be induced to undergo apoptosis in the absence of TCR signals by fas-fasL and TNF-TNFR interactions, but such TCR-independent mechanisms of apoptosis cannot be the basis for TCR-specific clonal deletion of DP thymocytes in vivo.
The CD28-dependent mechanism of apoptosis is a consequence of simultaneous TCR and CD28 coengagement on DP thymocytes and results exclusively in death of DP thymocytes that have simulataneously received both TCR and CD28 signals. Such apoptotic signals do not require the activity of PI 3-kinase, a signaling molecule associated with CD28 (69), but are resistant to the effects of cyclosporine A, a hallmark of CD28 involvement in mature T cells (70). Apoptosis induced by TCR-CD28 coengagement requires PKCγ and employs a common effector pathway involving caspases that is inhibitible by bcl-2. The present results are consistent with either of two possibilities: simultaneous TCR-CD28 signals induce DP thymocyte death either by directly initiating a novel intracellular apoptotic program or by inducing surface expression of an uncharacterized death receptor (e.g., a TNFR family member) that is engaged by surface ligands. In either case, the CD28-dependent mechanism of death requires that both TCR and CD28 signals be delivered simultaneously and requires that the death ligand, if it exists, be expressed on DP thymocytes for these were the only cells present in our cultures. We favor the possibility that TCR-CD28 directly signals an apoptotic program because we have found that TCR-CD28–induced apoptosis of DP thymocytes occurs efficiently at very low cell densities at which cell-cell interactions are unlikely to occur (data not shown). However, we cannot exclude the possibility that TCR/CD28 stimulation results in lethal death receptor/ligand interactions occurring in cis on the surface of individual DP thymocytes (Fig. 3 d).
The mechanism responsible for CD28-independent DP apoptosis is distinct from that of TCR-CD28–induced apoptosis. CD28-independent DP thymocyte apoptosis does not require costimulatory signals. Rather, TCR engagement alone on DP thymocytes appears sufficient to induce surface expression of a molecule which triggers death upon subsequent engagement by ligands expressed by APCs. This proposed surface molecule has features of death domain containing receptors, such as some members of the TNFR family. Thus, TCR signals may stimulate expression of a TNFR family member which is neither fas, nor CD30, nor 41BB, but which generates apoptotic signals when engaged by an appropriate ligand expressed or secreted by APC.
It is conceivable that all programmed cell death is initiated by signals transduced by death domains on specialized surface receptors. From this perspective, surface death receptors would be responsible for death of DP thymocytes stimulated either by TCR-CD28 costimulatory signals or by CD28-independent TCR signals alone. However, it is important to appreciate that the identity and specificity of the death receptors induced by TCR-CD28 signals must be different than those induced by TCR signals alone. This conclusion is based on our data showing that TCR-CD28– stimulated DP thymocytes kill themselves or each other, but do not kill TCR-stimulated DP bystander cells (Fig. 3,c). Rather, TCR-stimulated DP thymocytes are induced to die upon subsequent interaction with APCs (Fig. 7 b). Therefore, from the perspective that all cell death is mediated by death domain containing receptors, the ligand for TCR-CD28–induced death receptors must be expressed on DP thymocytes themselves, whereas the ligand for TCR induced death receptors is not expressed on DP thymocytes but is expressed on APCs.
The importance of APCs in inducing clonal deletion in the thymus has long been appreciated (8, 71–73). However, the mechanism by which APCs induce DP thymocyte apoptosis has not been fully understood. Here we show for the first time that APCs can induce death of TCR stimulated DP thymocytes in two distinct ways via two distinct sets of ligands. Our observation that TCR signals can induce DP thymocyte apoptosis by two different mechanisms is relevant to an understanding of clonal deletion of DP thymocytes during normal in vivo development. In Fig. 9 we illustrate a model of in vivo clonal deletion that is based on our present data. We propose that the two mechanisms of TCR-mediated DP apoptosis identified in this report represent two distinct strategies to rid the developing DP thymocyte repertoire of autoreactive specificities during thymocyte development (Fig. 9). Only DP thymocytes whose TCRs bind MHC–peptide complexes on cells expressing the CD28 ligands B7-1 or B7-2 will be killed as a consequence of TCR and CD28 coengagement. Because B7-1 and B7-2 are not expressed in the thymic cortex but are only expressed on APCs and medullary epithelial cells, this form of clonal deletion would be confined to DP thymocytes autoreactive to self-antigens encountered either at the corticomedullary junction, where most APCs are located, or on medullary epithelium. In contrast, high-affinity interactions of TCR on DP thymocytes with self-antigens in the cortex would induce expression of a surface molecule that “tags” DP thymocytes for future disposal (i.e., a “death tag”). Such DP thymocytes would not die in response to TCR engagement per se, but would travel through the cortex and enter the corticomedullary junction where they would encounter a “screen” of APCs constitutively expressing or secreting a ligand that bind the putative death tag and induce apoptosis.
This model provides thre main insights. First, apoptosis of DP thymocytes targeted for deletion occurs either at the corticomedullary junction (CMJ) or in the thymic medulla, regardless of whether DP cells encountered antigen in the cortex. As a result, DP thymocyte deletion requires that DP cells migrate out of the thymic cortex to the CMJ or medulla which is considered to be a consequence of positive selection. Thus, our model predicts that DP thymocytes can only be clonally deleted in vivo if they are first positively selected. Observations that TCR-mediated apoptosis is confined to the thymic medulla are consistent with this perspective (74–75). Indeed, only DP thymocytes dying of neglect appear to undergo apoptosis in the cortex (75).
Second, the model proposes that CD28-dependent and CD28-independent mechanisms of TCR-mediated DP apoptosis eliminate clones bearing TCR specific for distinct sets of antigens: the CD28-dependent mechanism disposes of TCR reactivities to APC and medullary antigens, whereas the indirect, CD28-independent mechanism of TCR-mediated DP apoptosis disposes of TCR reactivities to cortical antigens. Recently, experimental mice were generated in which expression of MHC class II was confined to cortical epithelium (76). Our model predicts that these experimental mice would lack the CD28-dependent mechanism of death because medullary cells expressing B7 (thymic APC or medullary epithelium) would lack MHC class II expression and fail to engage TCR on DP thymocytes. Indeed, T cells in these animals were not tolerant to self-antigens on Class II+ APCs. Importantly, while CD28-dependent clonal deletion is absent in these mice, our model predicts that the CD28-independent mechanism of clonal deletion should be intact, so that their CD4+ T cells would be tolerant to self-antigens expressed on class II+ cortical epithelium.
Third, the model predicts that there can be a delay between the receipt of a negative selecting TCR signal and the death of the cell by the CD28-independent mechanism. Thus, the presence of autoreactive TCR specificities among DP thymocytes is not necessarily indicative of a failure of negative selection.
Our efforts to define the molecular basis for CD28-dependent mechanisms of TCR-mediated DP apoptosis revealed that CD28 is surprisingly unique in its capacity to cooperate with TCR to directly produce apoptotic signals. Even molecules that have been described as augmenting proliferation of mature T cells, such as CD9, CD43, CD81, CD27, 41BB, and CD30, were not able to stimulate TCR-mediated death of DP thymocytes, so DP thymocyte apoptosis is not the result of simultaneous engagement of TCR with any costimulatory molecule. Rather, CD28 appears to generate unique second signals whose identities have not yet been elucidated. Interestingly, TCR-CD28–induced thymocyte apoptosis does not require the activity of PI 3-kinase, one molecule known to associate with CD28.
The identity of the APC-derived signals responsible for CD28-independent thymocyte apoptosis is not known. While such signals may well involve molecules containing death domains, this study has ruled out two attractive candidates, CD30 and 41BB (Fig. 1 b). However, proteins expressing death domains continue to be identified. In fact, three newly identified molecules containing death domains (DR-3, DR-4, and TRAMP) are expressed in lymphopoietic tissues (56–58).
Finally, it is important to draw a distinction between TCR-mediated apoptosis of DP thymocytes and the phenomenon of negative selection. Negative selection refers to any process that rids a developing T cell repertoire of an autospecificity. Although TCR-mediated clonal deletion of DP thymocytes is thought to be a major component of negative selection, it is clearly not the only mechanism responsible for negative selection. Indeed, we have previously shown that thymocytes can be developmentally arrested before the DP stage in response to TCR signals (3) and others have shown that negative selection can occur after the DP stage of development (77–79). In all likelihood the molecular mechanisms that operate at these other developmental stages (both pre- and post-DP) are distinct from those responsible for TCR-dependent apoptosis of DP thymocytes. In support of this possibility, it is interesting to note that (a) transgenic bcl-2 expression does not always affect negative selection (36) even though it abrogates clonal deletion of DP thymocytes and (b) fas appears to play a role in the TCR-mediated death of semimature T cells in the thymus (79) but clearly does not play a role in the TCR-mediated death of rigorously purified DP thymocytes.
In conclusion, this study identified both TCR-independent and TCR-dependent mechanisms of DP thymocyte apoptosis and reveals that TCR-dependent mechanisms of DP thymocyte death occur by two mechanisms: (a) a CD28-dependent mechanism in which TCR and CD28 costimulatory signals must be received simultaneously to generate apoptotic signals and (b) a CD28-independent mechanism in which TCR signals are indirectly responsible for apoptosis by upregulating molecules which, when subsequently engaged by APCs, will induce cell death. We propose that these two mechanisms represent two distinct strategies used by the thymus to dispose of autoreactive DP thymocytes and that the strategy used depends on where the antigen is encountered. Hence, DP thymocytes autoreactive to cortical antigens will be removed from the T cell repertoire by the indirect CD28-independent mechanism, whereas DP thymocytes autoreactive to APC or medullary cell antigens will be removed from the repertoire by CD28-dependent mechanisms (Fig. 9). Thus, the present study reveals an unexpected diversity of molecular mechanisms responsible for TCR-specific clonal deletion.
We are grateful to Drs. Eckhardt Podack, Philip J. Morrissey, Charles Janeway, and Karen Hathcock for generously providing reagents and mice; to Shabnam Shahabadi for excellent technical assistance; to Drs. Barbara Osborne, E. Wendy Shores, Susan Sharrow, and Pierre Henkart for critically reviewing the manuscript.
This report was supported in part by National Medical Research and Development Command EQ.0095.003.1412. The views expressed in the article are those of the authors and do not reflect the official policy or position of the Department of the Navy, Department of Defense, or the US Government.
Abbreviations used in this paper: CMJ, cortico medullary junction; DP, double positive; EtBr, ethidium bromide; fasL, fas ligand; FcR, Fc receptor; SP, single positive; TNFR, TNF receptor.
Address correspondence to Alfred Singer, Experimental Immunology Branch, NCI/NIH, Bldg 10, Rm 4B-17, Bethesda, MD 20892. Phone: 301-496-5461; Fax: 301-496-0887; E-mail: email@example.com Dr. Punt's current address is Haverford College, Haverford, Pennsylvania, 19041. Dr. Abe's current address is Research Institute for Biological Sciences, Science University of Tokyo, 2669 Yamazaki, Noda City, Chiba 278, Japan.