Ansorge S, Schön E
Forschungsabteilung Experimentelle Immunologie, Klinik für Innere Medizin, Medizinische Akademie Magdeburg, DDR.
Acta Histochem. 1987;82(1):41-6. doi: 10.1016/s0065-1281(87)80049-1.
Dipeptidyl peptidase IV (DP IV; E.C. 3.4.14.5), a plasma membrane structure of human T lymphocytes has been shown to be an important enzyme in the process of activation and proliferation of lymphocytes. In presence of specific inhibitors and antibodies against DP IV different functions of lymphocytes in vitro were found to be impaired. This holds true for mitogen and alloantigen induced DNA synthesis, immunoglobulin production and secretion, and interleukin-2 as well as interferon-gamma production. Studies of mitogen-induced expression of different activation markers (HLA class II antigen, 4F2, Tac) suggested that one of the functions of DP IV lies in overriding the cell cycle restriction point at G1. These data, together with other features of the DP IV, support the notion that this enzyme plays a key role in the modulation of lymphokine action by X-Pro- or X-Ala-directed limited proteolysis. Moreover the high frequency of DP IV susceptible bonds in different growth factors (e.g. IL-1, IL-2) and other biologically active peptides leads to the speculation that this peptidase is of more general significance to the regulation of cell growth.
二肽基肽酶IV(DP IV;E.C. 3.4.14.5),一种人T淋巴细胞的质膜结构,已被证明是淋巴细胞激活和增殖过程中的一种重要酶。在存在针对DP IV的特异性抑制剂和抗体的情况下,发现淋巴细胞在体外的不同功能受损。这适用于丝裂原和同种异体抗原诱导的DNA合成、免疫球蛋白的产生和分泌,以及白细胞介素-2和干扰素-γ的产生。对丝裂原诱导的不同激活标志物(HLA II类抗原、4F2、Tac)表达的研究表明,DP IV的功能之一在于跨越G1期的细胞周期限制点。这些数据,连同DP IV的其他特征,支持了这种酶通过X-脯氨酸或X-丙氨酸导向的有限蛋白水解在调节淋巴因子作用中起关键作用的观点。此外,不同生长因子(如IL-1、IL-2)和其他生物活性肽中DP IV敏感键的高频率出现,引发了这样的推测,即这种肽酶对细胞生长的调节具有更普遍的意义。