|Home | About | Journals | Submit | Contact Us | Français|
Peripheral T cell lymphomas (PTCLs) are highly aggressive malignancies with poor prognosis. Their molecular pathogenesis is not well understood and small animal models for the disease are lacking. Recently, the chromosomal translocation t(5;9)(q33;q22) generating the interleukin-2 (IL-2)–inducible T cell kinase (ITK)–spleen tyrosine kinase (SYK) fusion tyrosine kinase was identified as a recurrent event in PTCL. We show that ITK-SYK associates constitutively with lipid rafts in T cells and triggers antigen-independent phosphorylation of T cell receptor (TCR)–proximal proteins. These events lead to activation of downstream pathways and acute cellular outcomes that correspond to regular TCR ligation, including up-regulation of CD69 or production of IL-2 in vitro or deletion of thymocytes and activation of peripheral T cells in vivo. Ultimately, conditional expression of patient-derived ITK-SYK in mice induces highly malignant PTCLs with 100% penetrance that resemble the human disease. Our work demonstrates that constitutively enforced antigen receptor signaling can, in principle, act as a powerful oncogenic driver. Moreover, we establish a robust clinically relevant and genetically tractable model of human PTCL.
Peripheral T cell lymphomas (PTCLs) belong to the category of the most aggressive non-Hodgkin’s lymphomas with a high mortality rate, minimal effectiveness of conventional chemotherapy, and only 10–30% long-term survivors (Savage, 2007). PTCLU (PTCL unspecified) represents the largest PTCL subtype, and most patients present with advanced disease and frequent involvement of extranodal sites including spleen, bone marrow, liver, or blood. Pathologically, there is usually a diffuse infiltrate of atypical large T cells that exhibit an activated phenotype and a gene expression signature that resembles that of activated T cells (Piccaluga et al., 2007). Although PTCLs have a worse prognosis than aggressive B cell lymphomas, they are still largely treated the same way because rational treatment strategies for PTCL are currently missing (Escalón et al., 2005). The development of such strategies requires a better understanding of the molecular PTCL pathogenesis and, in addition, preclinical animal models for the human disease.
The chromosomal translocation t(5;9)(q33;q22) was recently identified as a recurrent and specific genomic alteration in PTCLU (Streubel et al., 2006). This translocation fuses the IL-2–inducible T cell kinase (ITK) and the spleen tyrosine kinase (SYK) genes. ITK and SYK are both required for normal antigen-induced lymphocyte activation. ITK is the predominant TEC kinase family member expressed in T cells (Berg et al., 2005). It possesses an aminoterminal pleckstrin homology (PH) domain for plasma membrane recruitment, a TEC homology (TH) domain, Src homology (SH) 3 and SH2 domains for association with T cell adapter proteins, and a kinase domain for TCR downstream signaling (Fig. 1 A). SYK is highly expressed in B lymphocytes and myeloid cells, where it plays essential roles for immune cell activation (Sada et al., 2001). It is also expressed in developing thymocytes (Palacios and Weiss, 2007). SYK contains tandem SH2 domains for ligand-induced association with the BCR or other ITAM (immunoreceptor tyrosine-based activation motif)–containing immunoreceptors and a kinase domain for the phosphorylation of receptor-proximal molecules and subsequent signal transduction (Fig. 1 A).
The translocation t(5;9)(q33;q22) fuses the PH and TH regions from ITK to the SYK kinase domain (Fig. 1 A; Streubel et al., 2006). However, the molecular and cellular consequences of ITK-SYK expression in lymphocytes are unknown. In this paper, we show that ITK-SYK is a catalytically active tyrosine kinase that constitutively engages the antigen receptor signaling machinery in T cells. Conditional expression of ITK-SYK in vivo induces highly aggressive T cell lymphomas with 100% penetrance and clinical and pathological features of the human PTCL. This work demonstrates that constitutively enforced antigen receptor signaling can act as a strong oncogenic driver in lymphoma pathogenesis and establishes a clinically relevant mouse model of human PTCL.
To study the role of ITK-SYK in lymphomagenesis, we isolated an ITK-SYK fusion transcript from a human tumor specimen harboring the t(5;9)(q33;q22) translocation (Streubel et al., 2006) and generated retroviral expression vectors that coexpress different ITK-SYK versions together with a GFP. In vitro kinase assays revealed that patient-derived ITK-SYK is an active tyrosine kinase (unpublished data). Exchange of lysine to arginine in the ATP binding pocket of the kinase domain (K262R; equivalent to K402R in wild-type SYK) resulted in a catalytically inactive ITK-SYKKD (kinase defective) version (unpublished data). To investigate functional roles of the ITK-SYK PH domain, we also introduced a point mutation into its lipid binding pocket by exchanging arginine 29 to cysteine (R29C; ITK-SYKPHmut). This mutation corresponds to the previously characterized R29C mutation in the PH domain of wild-type ITK that interferes with ITK membrane recruitment (Bunnell et al., 2000).
First, we transduced ITK-SYK and its variants into Jurkat cells to study effects on T cell signal transduction (Abraham and Weiss, 2004; Fig. 1 B). As a control, we used Jurkat cells that had been infected with a retrovirus expressing only GPF. Western blotting with an ITK-specific antibody demonstrated strong and constitutive expression of ITK-SYK and ITK-SYKKD in lipid rafts (Fig. 1 B). These are the subcellular fractions containing the membrane microdomains where TCR signaling is initiated (Dykstra et al., 2003). In contrast, the ITK-SYKPHmut version does as expected not associate with lipid rafts, although it is expressed in the nonraft fractions at a similar level to that of ITK-SYK or ITK-SYKKD.
In ITK-SYK–expressing cells, we detected tyrosine phosphorylation of several lipid raft–associated proteins including tyrosine phosphorylation of the TCR signal transducer PLCγ1 (Samelson, 2002). The pattern of tyrosine phosphorylation was similar to that of control Jurkat cells after stimulation with agonistic anti-CD3 and anti-CD28 antibodies to trigger antigen receptor signaling. Moreover, we observed a recruitment of endogenous ITK into the lipid rafts of ITK-SYK–expressing T cells as well as into rafts of cells that were stimulated via their TCR and CD28. In contrast, Jurkat cells that were transduced with ITK-SYKKD or ITK-SYKPHmut cells did not recruit ITK into lipid rafts and did not exhibit protein tyrosine phosphorylation above baseline. (Fig. 1 B).
Normal TCR signaling in Jurkat cells induces phosphorylation of the TCR-proximal adapters SLP-76 and LAT and subsequent activation of several downstream pathways, leading to the up-regulation of the activation marker CD69 and production of IL-2 (Samelson, 2002; Abraham and Weiss, 2004). To further study ITK-SYK signaling, we used intracellular flow cytometry with activation-specific antibodies directed against phosphorylated TCR signaling molecules (phosflow; Fig. 1 C). Constitutive ITK-SYK expression triggers tyrosine phosphorylation of SLP-76 and LAT. Again, PLC-γ1 phosphorylation was also detected. Moreover, we observed constitutive activation of the AKT, ERK, and p38 MAP kinase downstream pathways in ITK-SYK–expressing cells. The protein phosphorylation pattern correlated to that of control cells that were acutely stimulated with CD3 and CD28 antibodies (Fig. S1).
As cellular readouts for ITK-SYK function, we then monitored CD69 expression and IL-2 production (Fig. 1, D and E). Strong up-regulation of CD69 was detected in ITK-SYK–expressing cells, as well as in CD3/CD28-stimulated cells, but not in noninfected cells or cells infected with a GFP control virus (Fig. 1 D). The up-regulation of CD69 by ITK-SYK was dependent on both an intact kinase domain and an intact PH domain because ITK-SYKKD or ITK-SYKPHmut versions did not enhance CD69 expression.
ITK-SYK also triggered a profound production of IL-2, which was even higher than the IL-2 production induced by optimal CD3/CD28 costimulation with agonistic antibodies (Fig. 1 E). Similar to the up-regulation of CD69, the ITK-SYK–induced secretion of IL-2 required an intact ITK-SYK kinase and PH domain.
To investigate the importance of ITK-SYK kinase activity in an alternative way, we also tested whether ITK-SYK signaling might be sensitive to small molecule inhibition. To this end, we used the immunosuppressant wild-type SYK inhibitor R406 which is currently in clinical trails for inflammatory, autoimmune, and selected malignant diseases (Weinblatt et al., 2008; Friedberg et al., 2010). Both ITK-SYK–induced up-regulation of CD69 and IL-2 production were completely blocked by R406 treatment (Fig. 1, D and E).
Together, these first in vitro experiments indicate that ITK-SYK is a lipid raft–associated tyrosine kinase, which constitutively engages molecular components of the TCR signaling machinery and thereby mimics aspects of a TCR signal in the absence of a ligand. Because an SYK kinase inhibitor or inactivating mutations in the ITK-SYK kinase or PH domain block ITK-SYK signaling, we additionally conclude that both kinase activity and membrane recruitment are essential for productive ITK-SYK signal transduction.
Based on the association of ITK-SYK with human PTCLs, we particularly wanted to study the effects of ITK-SYK signaling in lymphocytes in vivo. To this end, we created a novel mouse model that allows ITK-SYK expression in a controlled and inducible fashion (Fig. 2). We introduced a human ITK-SYK fusion cDNA preceded by a loxP-flanked transcriptional and translational STOP cassette into the ubiquitously expressed Rosa26 locus using previously established gene targeting (Sasaki et al., 2006; Fig. 2, A and B). The resulting Rosa26loxSTOPlox-ITK-SYK mice were crossed to CD4-Cre transgenic animals (Lee et al., 2001) to induce T cell–specific excision of the STOP cassette and T cell–restricted ITK-SYK expression in the Rosa26loxSTOPlox-ITK-SYK × CD4-Cre double transgenic offspring (from now on called ITK-SYKCD4-Cre mice). As Cre-catalyzed recombination also induces enhanced GFP (eGFP) expression from an internal ribosomal entry site (IRES), we can visualize ITK-SYK–expressing cells. To induce ITK-SYK expression in the B cell lineage, we crossed the Rosa26loxSTOPlox-ITK-SYK line with CD19-Cre transgenic animals (Rickert et al., 1997; double-transgenic offspring called ITK-SYKCD19-Cre mice). FACS analysis in 5-wk-old animals revealed specific expression of the recombined ITK-SYK allele in >85% of peripheral T cells of ITK-SYKCD4-Cre mice or B cells in ITK-SYKCD19-Cre mice (Fig. 2 C). Expression of the ITK-SYK protein in the respective lymphocyte lineages was confirmed by Western blotting (Fig. 2 D).
We first focused on lymphocyte development in young (4–5-wk-old) animals. The CD4-Cre transgene mediates loxP recombination at the CD4+CD8+ double-positive (DP) stage of thymocyte development and continues in single-positive (SP) cells (Lee et al., 2001). The DP stage is the period of T cell differentiation, when thymocytes expressing autoreactive TCRs receive strong TCR signals and are subsequently deleted by negative selection to prevent autoimmunity (Sebzda et al., 1999). As expected, ITK-SYK expression was observed at the DP stage in ITK-SYKCD4-Cre mice (Fig. 3 A), leading to a profound reduction in the frequencies and absolute numbers of DP thymocytes in these animals (Fig. 3, B and C). These findings are consistent with the hypothesis that ITK-SYK imitates features of a strong TCR signal, as observed in our in vitro experiments in Fig. 1. The decrease in DP cells is followed by a diminishment of the SP populations (Fig. 3 C) and reduced numbers (Fig. 3 D) and frequencies (Fig. 3 E) of mature peripheral T cells. Still, the majority of the peripheral CD4+ and CD8+ T cells express the fusion kinase (Fig. 3 F; Fig. 2, C and D; and not depicted). These ITK-SYK–expressing CD4+ and CD8+ peripheral T cells exhibit an activated phenotype, which is characterized by a large cell size, high expression of the activation marker CD44, and low expression of CD62L (Fig. 3 G). Furthermore, these cells show down-regulated TCR-β surface expression. Histological in vivo analysis revealed that these activated T cells are highly proliferative but do not undergo apoptosis, as determined by Ki-67 immunohistochemistry and staining for active Caspase-3 (Fig. S2). Moreover, ITK-SYK–expressing T cells exhibit tyrosine phosphorylation of multiple lipid raft–associated proteins, including PLC-γ1, that is similar to wild-type T cells that are stimulated via the TCR with anti-CD3/CD28 antibodies (Fig. 3 H and not depicted). B cell development was not affected in ITK-SYKCD4-Cre mice (Fig. 3 D and not depicted).
To test whether B cell–intrinsic expression of ITK-SYK would influence B cell development or activation, we analyzed ITK-SYKCD19-Cre mice. In these animals, we observed an onset of B cell–specific ITK-SYK expression in the bone marrow and high percentages of ITK-SYK–expressing B cells in all peripheral B cell compartments including follicular, marginal zone, and B1 B cells (Fig. 4 A; Fig. 2, C and D; and not depicted). However, the overall protein tyrosine phosphorylation pattern did not differ between wild-type and ITK-SYK–expressing B lymphocytes (Fig. 4 B). Moreover, we did not detect any effects of B cell–intrinsic ITK-SYK expression on the total B cell numbers (Fig. 4 C), the frequencies of individual B cell subsets (Fig. 4 D and not depicted), B cell size, or activation status (Fig. 4 E and not depicted). Thus, although the TCR and BCR share many molecular features of downstream signaling (Myung et al., 2000), enforced B cell–specific expression of ITK-SYK has apparently no overt effects on B cell biology.
We hypothesized that the fundamentally different functions of ITK-SYK in the T and B cell lineage could, in part, be the result of a cell type–specific localization of the fusion kinase into subcellular compartments because the protein region that is responsible for membrane recruitment originates from the T cell kinase ITK. Indeed, although T cells from ITK-SYKCD4-Cre mice and B cells from ITK-SYKCD19-Cre mice express similar amounts of ITK-SYK in cytoplasmic nonraft fractions, the association of ITK-SYK with lipid rafts is only observed in T and not in B cells (Fig. 4 F). Similar to that seen in Fig. 1 B, ITK-SYK expression in T cells also induces recruitment of wild-type ITK into lipid rafts. Thus, the combined analysis of ITK-SYKCD4-Cre and ITK-SYKCD19-Cre mice demonstrates that ITK-SYK mimics a strong antigen receptor signal in primary T cells but not in B cells in vivo. The results additionally indicate that ITK-SYK depends on an appropriate cellular microenvironment for productive signaling.
To investigate potential oncogenic roles of ITK-SYK, we were especially interested in the long-term consequences of ITK-SYK expression in vivo. Therefore, we followed cohorts of ITK-SYKCD4-Cre (n = 19) and ITK-SYKCD19-Cre mice (n = 8) and regularly determined the frequencies of eGFP+ ITK-SYK–expressing T or B cells in their peripheral blood (Fig. 5 A). The percentages of ITK-SYK–expressing T cells increased continuously in ITK-SYKCD4-Cre mice and rose up to almost 100%, indicating a profound T cell lymphoproliferative disorder. Starting at ~12 wk of age, the animals became overtly ill and eventually developed wasting and runting symptoms, lethargy, hunched postures, and distended abdomens. We had to sacrifice several mice from this series for ethical reasons. However, the medium frequency of ITK-SYK–expressing B cells in ITK-SYKCD19-Cre mice stayed constant during that time (Fig. 5 A).
Next, we obtained survival curves from ITK-SYKCD4-Cre (n = 73) and control mice (n = 15; Fig. 5 B). Although all ITK-SYKCD4-Cre animals succumbed to disease or had to be euthanized within 27 wk of age, the control mice did not develop any pathological symptoms.
To characterize the disease in ITK-SYKCD4-Cre mice in detail, we sacrificed animals at 20 wk of age or upon disease signs. All spleens of ITK-SYKCD4-Cre mice were massively enlarged (Fig. 5 C) and consisted mainly of ITK-SYK–expressing TCR-β+ and eGFP+ T cells with an activated phenotype (Fig. 5 D and not depicted; n = 40 mice analyzed). Histological analysis revealed a complete disruption of the normal spleen architecture by a diffuse infiltrate of medium- to large-sized lymphoid cells that exhibited irregular nuclei, prominent nucleoli, and high mitotic rates strongly suggestive of a neoplastic growth (Fig. 6 A). Ki-67 staining further demonstrated a high proliferation (Fig. 6 A). The abnormal T cell populations were primarily CD4+ in ~61% of the animals (Type I), predominantly CD8+ in 23% (Type II), and a mix of CD4+ and CD8+ T cells in the remaining mice (Type III; Fig. 6 B). The atypical lymphoid cells always infiltrated the bone marrow (Fig. 6 C) and grew invasively into solid organs, including kidneys, livers, and lungs (Fig. 6 D). Immunohistochemical analysis with anti-CD3 antibodies confirmed the T cell nature of the infiltrate (Fig. 6 D). To characterize clonality, we analyzed their TCR-Vβ chain repertoire by flow cytometry (Fig. 6 E). The repertoire was always skewed and consistently enriched for individual TCR-Vβ clones (n = 33 mice analyzed). Although the specifically expanded TCR-Vβ chain clones differed among distinct animals, we regularly observed that the identical T cell clones infiltrated all tested tissues in one individual mouse. To further study T cell clonality, we performed a PCR-based and computer-assisted fragment length analysis (Genescan) for TCR-β and TCR-γ locus gene rearrangements (Kneba et al., 1995; van Dongen et al., 2003). Clonal TCR rearrangements were detected in all tested diseased ITK-SYKCD4-Cre (n = 3) but not in CD4-Cre control mice (n = 4; Fig. 6 F and not depicted).
Finally, we tested whether ITK-SYK–induced T cell tumors could be transplanted. To this end, we injected ITK-SYK–expressing T cells from affected animals intravenously into recipient mice. Tail blood analysis documented that the transplanted cells could massively expand in the recipients (Fig. 7 A). Morphological and flow cytometric analyses again revealed a lethal infiltration into lymphoid and nonlymphoid organs that was identical to the original disease (Fig. 7, B–D). Thus, enforced ITK-SYK expression in the T cell lineage induces a highly aggressive transplantable T cell lymphoma with a malignant growth pattern that resembles the clinical and pathological features of human PTCL (Cotta and Hsi, 2008).
Human cancers do not arise from oncogene expression throughout an entire cell lineage but are caused by somatic mutations in single tumor cell precursors. Surprisingly, we observed that all ITK-SYKCD19-Cre mice eventually also developed a lethal wasting syndrome (Fig. 8 A) with splenomegaly (Fig. 8 B) and infiltration of abnormal lymphocytes into multiple organs (Fig. 8, C and D). Although the CD19-Cre transgene induces very efficient and highly selective ITK-SYK expression in the B cell lineage (Fig. 2, C and D; and Fig. 4), the lymphomas in ITK-SYKCD19-Cre mice were, intriguingly, all of T cell origin and macroscopically and microscopically indistinguishable from the T cell lymphomas in ITK-SYKCD4-Cre mice. They consisted of enlarged, activated, and highly proliferative Ki-67+ and TCR-β+ ITK-SYK–expressing cells (Fig. 8, C–E; and not depicted), which could transmit the disease to recipients in transplantation experiments (not depicted). However, in contrast to ITK-SYKCD4-Cre mice we never observed mixed CD4+ and CD8+ infiltrates in ITK-SYKCD19-Cre mice but, instead, always homogenous tumor cell populations that express either CD4, in 75% of the cases (Type I), or CD8 (Type II; Fig. 8 F) and which were of clonal origin, as determined by surface staining for TCR-Vβ chains (Fig. 8 G; n = 12) or Genescan analysis (n = 5; not depicted). We therefore conclude that a rare and untypical expression of ITK-SYK in the T cell lineage of ITK-SYKCD19-Cre mice, presumably as a result of “leaky” Cre expression, is able to drive neoplastic transformation and malignant expansion of single T cell clones, which closely models the pathophysiological situation in human PTCL patients.
Chromosomal translocations in hematological malignancies have always provided key insights into disease pathogenesis. Although some specific translocations are rare, the signaling pathways that are deregulated by these events are regularly hit by alternative genetic mechanisms such as mutations or amplifications in translocation negative cases or other tumor subentities (Fröhling and Döhner, 2008). As these aberrant signals directly trigger tumorigenesis they constitute rational targets for therapeutic interventions.
We demonstrate that the human PTCL-associated fusion tyrosine kinase ITK-SYK triggers molecular and cellular features of strong TCR signaling in vitro and in vivo. These events include tyrosine phosphorylation of TCR-proximal proteins, activation of downstream cascades, and functional outcomes that, similar to normal antigen receptor signaling, depend on the cellular context. Examples are deletion of DP thymocytes or activation of T cells in the periphery. Therefore, our results indicate that ITK-SYK acts as an intracellular mimic of a strong antigen receptor signal. Yet ITK-SYK signaling is certainly not identical to ligand-induced TCR signaling and differs in terms of kinetics and some quantitative aspects like induction of maximal IL-2 production. Moreover, normal TCR signaling is regularly terminated at the end of an immune response, whereas ITK-SYK signaling is chronic. Ultimately, ITK-SYK induces highly malignant PTCLs with 100% penetrance. The fact that the tumors are clonal suggests that cooperating events contribute to proliferative advantage and outgrowth of individual lymphoma cell clones. Notably, sporadic ITK-SYK expression in single T cells of ITK-SYKCD19-Cre mice drives oncogenesis, indicating that ITK-SYK is a bona fide oncogene. Secondary oncogenic events might also contribute to lymphoma development in ITK-SYKCD19-Cre mice.
Although the ITK-SYK fusion kinase is only found in a subset of PTCL patients (Streubel et al., 2006), a recent study with >140 PTCL samples reported aberrant expression of activated SYK in >90% of the cases (Feldman et al., 2008). Moreover, PTCL cells regularly exhibit characteristics of activated T cells including their gene expression signatures (Piccaluga et al., 2007; Savage, 2007). Together with our experimental results, these clinical findings suggest that an aberrant activation of antigen receptor signaling pathways could be a common driver of PTCL pathogenesis.
Antigen-mediated TCR ligation induces a recruitment of the SYK family member ZAP-70 to the receptor complex for LAT and SLP-76 phosphorylation and subsequent cell activation (Samelson, 2002). ITK-SYK is constitutively associated with lipid rafts and, as such, is presumably in constant proximity to its key substrates. The localization of ITK-SYK into the proper T cell microdomains is mediated via the PH domain and also potentially via the TH domain, which both originate from the T cell kinase ITK (Berg et al., 2005). These protein modules are known to coordinate membrane localization and binding to SLP-76 and LAT in a remarkably selective manner, as ITK does not efficiently interact with related B cell molecules including SLP-65 (Hashimoto et al., 1999; Su et al., 1999; Bunnell et al., 2000). This might explain why B cell–intrinsic expression of ITK-SYK has no apparent effects in the B cell lineage. Consistent with our findings, ITK-SYK kinase activity and membrane localization are also required for ITK-SYK–mediated transformation of an immortalized fibroblast cell line in vitro (Rigby et al., 2009). Together, these results suggest that therapeutic strategies for ITK-SYK inhibition could either target the ITK-SYK kinase activity or try to interfere with ITK-SYK localization. Our experiments in Jurkat cells demonstrated that the SYK kinase inhibitor R406 can very potently block ITK-SYK signaling. Still, it is currently unclear whether constitutive ITK-SYK signaling is predominantly responsible for tumor initiation or also essential for disease maintenance. Thus, studies are necessary that investigate the responsiveness of ITK-SYK–induced lymphoma to R406 treatment in vivo.
Aberrant antigen receptor signaling is frequently observed in human lymphoid malignancies beyond PTCL. Chronic active BCR signaling was recently described in diffuse large B cell lymphomas (Davis et al., 2010). Other lymphoma entities with aberrant activities of antigen receptor signaling pathways are chronic lymphocytic leukemias, which regularly show aberrant ZAP-70 expression, mucosa-associated lymphoid tissue lymphomas, which often develop in the context of chronic antigenic stimulation, or follicular lymphoma (Küppers, 2005). Our study provides in vivo evidence that constitutively enforced antigen receptor signals are directly able to induce oncogenesis. The downstream signaling cascades that are critical for lymphoma initiation or maintenance are not well defined. The presented mouse models will serve as valuable tools to genetically dissect these pathways in vivo. Finally, in addition to the mentioned SYK inhibitor, several small molecule drugs, which interfere with antigen receptor signaling, are already available or are in preclinical or clinical development for malignant or nonmalignant immune-mediated diseases. Our clinically relevant PTCL model will help to identify compounds that could be of potential use for the treatment of PTCLs. In light of the minimal effectiveness of conventional chemotherapy in PTCL treatment such studies are urgently warranted.
Human ITK-SYK cDNA (Streubel et al., 2006) was cloned into a Rosa26 targeting vector (Sasaki et al., 2006), linearized, and electroporated into E14K embryonic stem cells as previously described (Ruland et al., 2001). Successful homologous recombination at the Rosa26 locus was confirmed by standard Southern blot analysis using a 5′ flanking probe as previously described (Ruland et al., 2001). Blastocyst injection of two independent clones and subsequent chimera breeding resulted in Rosa26loxSTOPlox-ITK-SYK mice. Rosa26loxSTOPlox-ITK-SYK mice were crossed with either CD4-Cre (Lee et al., 2001) or CD19-Cre mice (Rickert et al., 1997). Littermates were used in all subsequent experiments. Athymic Foxn1nu/nu mice purchased from Harlan were used as recipients in transplantation experiments. Studies were conducted according to federal and institutional guidelines. Animal protocols were approved by the government of Upper Bavaria.
Retroviral constructs were generated by cloning ITK-SYK, ITK-SYK (K262R) (ITK-SYKKD), or ITK-SYK (R29C) (ITK-SYKPHmut) cDNA into IRES GFP containing MSCV-based vectors using standard molecular biology techniques as previously described (Grundler et al., 2005). Retroviral particles were generated upon transfection of Phoenix-E packaging cells as previously described (Grundler et al., 2005).
Jurkat cells were cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum. Phoenix-E packaging cells were maintained in DME supplemented with 10% fetal bovine serum. The SYK inhibitor R406 (Rigel Pharmaceuticals) was used at a final concentration of 2 µM where indicated.
Cell supernatants from Jurkat cells were harvested 36 h after retroviral infection and CD3 (10 µg/ml)/CD28 (2 µg/ml) stimulation as indicated. IL-2 concentrations were determined via ELISA (OptEIA Human IL-2 ELISA Set; BD).
For protein analysis, T or B cells from spleen or lymph nodes were isolated by negative selection with magnetic beads (Dynabeads; Invitrogen) and antibodies against CD11b, B220, or Thy1.2 as previously described (Ferch et al., 2007).
107 Jurkat cells or 5 × 107 purified lymphocytes per assay point were kept unstimulated or stimulated with 5 µg/ml CD3/1 µg/ml CD28 for 5 min as indicated and subsequently lysed in Brij lysis buffer as previously described (Ferch et al., 2007). Mice older than 12 wk were used for T cell preparations to obtain sufficient numbers of ITK-SYK–expressing T lymphocytes. Postnuclear supernatants were mixed with 85% (wt/vol) sucrose, overlaid with 35% (wt/vol) and 5% (wt/vol) sucrose, and separated by ultracentrifugation. Lipid raft and cytoplasmatic fractions were analyzed for the presence of the lipid raft marker GM1 (Ferch et al., 2007).
For whole cell protein analysis, Jurkat cells or primary lymphocytes were lysed with CHAPS buffer and subsequently subjected to Western blot analysis as previously described (Ferch et al., 2007). Alternatively, lipid raft or nonraft fractions were analyzed. The following antibodies were used: anti-Emt (2F12; mouse monoclonal; Santa Cruz Biotechnology, Inc.) for ITK or ITK-SYK detection, anti–phospho-tyrosine (P-Tyr-100; mouse monoclonal; Cell Signaling Technology), anti–phospho-PLCγ1 (Tyr783; rabbit polyclonal; Cell Signaling Technology), and anti-β-actin (20–33; Sigma-Aldrich).
FACS analysis was performed using standard protocols (Ferch et al., 2007). In brief, Jurkat cells were either surface stained with anti-human CD69 antibody or intracellularly stained after permeabilization with 70% ice-cold methanol with antibodies against phosphorylated forms of SLP-76 (pY128), LAT (pY171), PLCγ1 (pY783), AKT (pS473), ERK1/2 (pT202/pY204), or p38 (pT180/pY182). Primary cell suspensions from thymus, spleen, lymph nodes, bone marrow, or peripheral blood were directly labeled. Single cell suspensions from liver, kidney, or lung were first purified by Percoll gradient centrifugation. Fluorescently labeled antibodies against the following surface proteins were used for mouse cell staining: B220 (RA3_6B2); TCR-β (H57-597); CD3 (1452C11); CD4 (Gk1.5); CD5 (53–7.3); CD8 (53–6.7); CD21/35 (7G6); CD23 (B3B4); CD44 (IM7); CD62L (MEK-14); CD86 (GL1); IgM (II/41), Vβ3-TCR (KJ25), Vβ4-TCR (CTVB4), Vβ6-TCR (RR4-7), Vβ7-TCR (TR310), Vβ8.1/8.2-TCR (MR5-2), Vβ8.3-TCR (CT-8C1), Vβ10b-TCR (CTVB10b), Vβ11-TCR (CTVB11), and Vβ12b-TCR (CTVB12b). Data were acquired on a FACSCalibur or FACSCanto II flow cytometer (BD). FlowJo Software (Tree Star, Inc.) was used for data analysis.
All organs were fixed in 4% formaldehyde and paraffin embedded. 3–5-µm-thick sections were cut and stained with H&E. Immunohistochemistry was performed on an automated immunostainer (Ventana Medical Systems, Inc.) according to the company’s protocols for open procedures with slight modifications. The antibody panel used included CD3 (SP7; Thermo Fisher Scientific), B220 (BD), Ki-67 (SP6; Thermo Fisher Scientific), and cleaved Caspase 3 (ASP 175; Cell Signaling Technology). Appropriate positive controls were used to confirm the adequacy of the staining.
Genomic DNA was extracted from total splenic cell suspensions of diseased ITK-SYKCD4-Cre, ITK-SYKCD19-Cre, or control mice (CD4-Cre or CD19-Cre, respectively). V-D-J and incomplete D-J rearrangements of the TCR-β locus were analyzed via five individual PCR reactions with the following primer combinations: Vβ(1–20)-Jβ1, Vβ(1–20)-Jβ2, Dβ1-Jβ1, Dβ2-Jβ2, and Dβ1-Jβ2. Primer sets consisted of a mixture of 20 family-specific upstream primers located within the Vβ gene segments or consensus primers immediately located 5′ of the Dβ1/Dβ2 rearrangement and 5′FAM-labeled consensus primers immediately located 3′ of the Jβ1/Jβ2 rearrangement as previously described (Gärtner et al., 1999). TCR-γ locus rearrangement was analyzed with a PCR reaction using a Vγ4 and a 5′-FAM–labeled Jγ1 consensus primer as described (Kawamoto et al., 2000). 5′-FAM–labeled PCR products were size separated by capillary POP-7-Polymer electrophoresis and visualized via automated scanning by using a 3700 Genetic Analyzer (Applied Biosystems). Reagents were all obtained from Applied Biosystems. Fragment size distribution was determined by GeneMapper software (Applied Biosystems) and analyzed as previously described (Kneba et al., 1995; van Dongen et al., 2003).
6-wk-old athymic Foxn1nu/nu mice (Harlan) were intravenously injected with 1.5 × 107 splenocytes isolated from diseased ITK-SYKCD4-Cre or ITK-SYKCD19-Cre mice. Recipients were monitored daily for signs of disease and blood samples were analyzed by FACS at the indicated time points.
Where indicated, results were analyzed for statistical significance with the unpaired two-tailed Student’s t test. Differences between groups were considered as significant at p-values <0.05.
Fig. S1 shows results from phosflow experiments investigating the phosphorylation status of TCR signaling molecules upon CD3/CD28 stimulation in retrovirally infected Jurkat cells. Fig. S2 presents the immunohistochemical expression analysis of CD3, Ki-67, and the active form of Caspase 3 (Caspase 3A) in spleen sections from of 4–5-wk-old ITK-SYKCD4-Cre or control CD4-Cre animals. Online supplemental material is available at http://www.jem.org/cgi/content/full/jem.20092042/DC1.
We thank Marc Schmidt-Supprian for plasmids and helpful discussions, Rigel Inc. for providing the SYK inhibitor R406, Stefan Wanninger, Vera Pfänder, Claudia Kloss, and Susanne Weiss for cloning and excellent technical assistance, and Gisela Keller for access to gene scan equipment.
This work was supported by Sonderforschungsbereich grants from Deutsche Forschungsgemeinschaft to L. Quintanilla-Martinez and J. Ruland and by a Max-Eder-Program grant from Deutsche Krebshilfe to J. Ruland.
The authors have no conflicting financial interests.