Kanner S B, Odum N, Grosmaire L, Masewicz S, Svejgaard A, Ledbetter J A
Bristol-Myers Squibb Pharmaceutical Research Institute, Seattle, WA 98121.
J Immunol. 1992 Dec 1;149(11):3482-8.
Bacterial enterotoxin superantigens bind directly to HLA class II molecules (HLA-DR) expressed on both APC and activated human T cells, and simultaneously bind to certain V beta chains of the TCR. In this report, we compared early T cell signaling events in human alloantigen-stimulated T cells when activated by HLA-DR ligation through antibody cross-linking or by direct enterotoxin superantigen binding. Both types of stimuli induced tyrosine phosphorylation of phosphatidylinositol-specific phospholipase C gamma 1 (PLC gamma 1) and an increase in intracellular calcium concentration; however, superantigen-induced signaling was stronger than class II ligation alone. Antibody-mediated ligation of HLA-DR with CD3 resulted in augmented PLC gamma 1 activation and increased calcium mobilization, consistent with a mechanism of superantigen activity through a combination of class II and CD3/Ti signals. In addition, down-modulation of CD3 receptors with antibody demonstrated that superantigen-induced signaling events were CD3-dependent. Superantigen signaling was also class II-dependent, in that resting T cells were not responsive to direct enterotoxin stimulation. To address how early signal transducing activity correlated with T cell responsiveness, alloantigen-primed T cells were activated with immobilized class II-specific mAb or soluble superantigen. Both HLA-DR mAb-stimulated T cells and enterotoxin-treated T cells proliferated strongly in response to co-stimulation by a combination of CD28 receptor engagement and PMA addition. In addition, superantigen-induced growth was induced by CD28 receptor ligation with antibody or the B7 counter-receptor expressed on Chinese hamster ovary cells. Taken together, these results indicate that class II molecules expressed on activated T cells are directly coupled to the PLC gamma 1 signal transduction pathway, and that coligation of HLA-DR with CD3 augments T cell signaling comparable to that induced by enterotoxin superantigen. Thus, we suggest that superantigen-induced early signaling responses in activated T cells may be due in part to class II transmembrane signals induced when HLA-DR and V beta are ligated in cis.
细菌肠毒素超抗原直接结合在抗原呈递细胞(APC)和活化的人T细胞上表达的II类组织相容性抗原(HLA - DR)分子,同时结合T细胞受体(TCR)的某些Vβ链。在本报告中,我们比较了人同种异体抗原刺激的T细胞在通过抗体交联进行HLA - DR连接激活或通过直接肠毒素超抗原结合激活时的早期T细胞信号传导事件。两种刺激均诱导磷脂酰肌醇特异性磷脂酶Cγ1(PLCγ1)的酪氨酸磷酸化并导致细胞内钙浓度升高;然而,超抗原诱导的信号传导比单独的II类连接更强。抗体介导的HLA - DR与CD3连接导致PLCγ1活化增强和钙动员增加,这与通过II类和CD3/Ti信号组合的超抗原活性机制一致。此外,用抗体下调CD3受体表明超抗原诱导的信号传导事件是CD3依赖性的。超抗原信号传导也是II类依赖性的,因为静止的T细胞对直接肠毒素刺激无反应。为了研究早期信号转导活性与T细胞反应性之间的关系,用固定化的II类特异性单克隆抗体或可溶性超抗原激活同种异体抗原致敏的T细胞。HLA - DR单克隆抗体刺激的T细胞和肠毒素处理的T细胞在通过CD28受体结合和添加佛波酯(PMA)的联合共刺激下均强烈增殖。此外,超抗原诱导的生长是由抗体与CD28受体连接或中国仓鼠卵巢细胞上表达的B7反受体诱导的。综上所述,这些结果表明活化T细胞上表达的II类分子直接与PLCγ1信号转导途径偶联,并且HLA - DR与CD3的共连接增强了与肠毒素超抗原诱导的T细胞信号传导相当的信号传导。因此,我们认为活化T细胞中超抗原诱导的早期信号反应可能部分归因于当HLA - DR和Vβ顺式连接时诱导的II类跨膜信号。