Suppr超能文献

CD26/二肽基肽酶IV在某一大鼠品系的T细胞活化中真的是一个重要分子吗?

Is CD26/dipeptidyl peptidase IV a really important molecule in T cell activation of a certain rat strain?

作者信息

Iwaki-Egawa S, Watanabe Y, Fujimoto Y

机构信息

Department of Clinical Biochemistry, Hokkaido Institute of Pharmaceutical Sciences, Otaru, Japan.

出版信息

Immunobiology. 1995 Nov;194(4-5):429-42. doi: 10.1016/S0171-2985(11)80109-9.

Abstract

A new monoclonal antibody (MS-7 mAb) was raised to investigate the real role of the membrane-associated molecule CD26/dipeptidyl peptidase IV (DPP IV; EC 3.4.14.5), which transduces activation signals in T cells. A strain of rats which is deficient in DPP IV was used. MS-7 mAb recognized DPP IV (110 kDa) and its 60 kDa fragment, starting at the 281st residue corresponding to the extracellular one comprising the active-site sequence Gly-X-Ser631-X-Gly of DPP IV. MS-7 mAb recognized CD26 on T cells of DPP IV+ rats both before and after mitogen activation. CD26 expression and DPP IV enzyme activity are increased on T cells following their activation; nevertheless, no CD26 was expressed on T cells of DPP IV- rats, and no DPP IV enzyme activity was detected either before or after mitogen activation. In addition, MS-7 mAb inhibited the mitogen-stimulated proliferation of DPP IV+ rats, but did not affect that of DPP IV- rats. These results suggest that CD26/DPP IV is not a necessary molecule in T cell activation, and that there is some other bypass in T cell activation of DPP IV- rats.

摘要

为了研究膜相关分子CD26/二肽基肽酶IV(DPP IV;EC 3.4.14.5)在T细胞中传导激活信号的实际作用,制备了一种新的单克隆抗体(MS-7单克隆抗体)。使用了一种DPP IV缺陷的大鼠品系。MS-7单克隆抗体识别DPP IV(110 kDa)及其60 kDa片段,该片段从对应于包含DPP IV活性位点序列Gly-X-Ser631-X-Gly的细胞外部分的第281个残基开始。MS-7单克隆抗体识别有丝分裂原激活前后DPP IV+大鼠T细胞上的CD26。T细胞激活后,其CD26表达和DPP IV酶活性增加;然而,DPP IV-大鼠的T细胞上不表达CD26,有丝分裂原激活前后也未检测到DPP IV酶活性。此外,MS-7单克隆抗体抑制DPP IV+大鼠有丝分裂原刺激的增殖,但不影响DPP IV-大鼠的增殖。这些结果表明,CD26/DPP IV不是T细胞激活中的必需分子,并且在DPP IV-大鼠的T细胞激活中存在一些其他旁路。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验