Membrane-bound peptidases of lymphocytes: functional implications.

Biomedica biochimica acta Pub Date : 1991-01-01
S Ansorge, E Schön, D Kunz
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引用次数: 0

Abstract

The paper is aimed towards the role of the membrane ecto-enzymes aminopeptidase N (CD13, AP-N) and dipeptidyl peptidase IV (CD26, DP IV) in the immune system. Both peptidases have been identified on T lymphocytes, AP-N also on monocytes and non-T cells. Using enzyme inhibitors and antibodies it has been shown by different groups that DP IV plays a key role in T cell activation and growth. Inhibition studies of our laboratory, using bestatin, actinonin and probestin, also demonstrated an essential role of AP-N in regulation of T cell growth. Moreover, the action of cytokines/lymphokines having DP IV susceptible bonds, as IL-1, IL-2 and IL-6, on lymphocyte proliferation, was found to be suppressed by specific inhibitors of DP IV as well as AP-N. These results are in favour of our hypothesis that DP IV and AP-N, possibly both in a concerted action, are involved in cytokine/lymphokine mediated signalling between immune cells.

淋巴细胞的膜结合肽酶:功能意义。
本文旨在探讨膜外酶氨基肽酶N (CD13, AP-N)和二肽基肽酶IV (CD26, DP IV)在免疫系统中的作用。这两种肽酶都在T淋巴细胞上发现,AP-N也在单核细胞和非T细胞上发现。利用酶抑制剂和抗体,不同的研究小组已经证明,DP IV在T细胞的激活和生长中起着关键作用。我们实验室使用bestatin, actionin和probestin进行的抑制研究也证明了AP-N在调节T细胞生长中的重要作用。此外,具有DP IV敏感键的细胞因子/淋巴因子,如IL-1、IL-2和IL-6,对淋巴细胞增殖的作用被DP IV和AP-N的特异性抑制剂所抑制。这些结果支持我们的假设,即DP IV和AP-N可能共同参与免疫细胞间细胞因子/淋巴因子介导的信号传导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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