Baum P R, Gayle R B, Ramsdell F, Srinivasan S, Sorensen R A, Watson M L, Seldin M F, Baker E, Sutherland G R, Clifford K N
Department of Gene Expression, Immunex R&D Corporation, Seattle, WA 98101.
EMBO J. 1994 Sep 1;13(17):3992-4001. doi: 10.1002/j.1460-2075.1994.tb06715.x.
A ligand was cloned for murine OX40, a member of the TNF receptor family, using a T cell lymphoma cDNA library. The ligand (muOX40L) is a type II membrane protein with significant identity to human gp34 (gp34), a protein whose expression on HTLV-1-infected human leukemic T cells is regulated by the tax gene. The predicted structures of muOX40L and gp34 are similar to, but more compact than, those of other ligands of the TNF family. Mapping of the muOX40L gene revealed tight linkage to gld, the FasL gene, on chromosome 1. gp34 maps to a homologous region in the human genome, 1q25. cDNAs for human OX40 receptor were cloned by cross-hybridization with muOX40, and gp34 was found to bind the expressed human receptor. Lymphoid expression of muOX40L was detected on activated T cells, with higher levels found on CD4+ rather than CD8+ cells. The cell-bound recombinant ligands are biologically active, co-stimulating T cell proliferation and cytokine production. Strong induction of IL-4 secretion by muOX40L suggests that this ligand may play a role in regulating immune responses. In addition, the HTLV-1 regulation of gp34 suggests a possible connection between virally induced pathogenesis and the OX40 system.
利用T细胞淋巴瘤cDNA文库克隆了小鼠OX40(肿瘤坏死因子受体家族成员)的配体。该配体(muOX40L)是一种II型膜蛋白,与人类gp34有显著同源性,gp34是一种在HTLV - 1感染的人类白血病T细胞上的表达受tax基因调控的蛋白。muOX40L和gp34的预测结构与肿瘤坏死因子家族的其他配体相似,但更紧凑。muOX40L基因的定位显示其与位于1号染色体上的FasL基因gld紧密连锁。gp34定位于人类基因组中的同源区域1q25。通过与muOX40交叉杂交克隆了人类OX40受体的cDNA,并发现gp34能与表达的人类受体结合。在活化的T细胞上检测到muOX40L的淋巴样表达,在CD4 +细胞上的水平高于CD8 +细胞。细胞结合的重组配体具有生物活性,可共同刺激T细胞增殖和细胞因子产生。muOX40L对IL - 4分泌的强烈诱导表明该配体可能在调节免疫反应中起作用。此外,gp34受HTLV - 1调控提示病毒诱导的发病机制与OX40系统之间可能存在联系。