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降钙素基因相关肽对有丝分裂原刺激的T淋巴细胞增殖的抑制作用。

Inhibition of mitogen-stimulated T lymphocyte proliferation by calcitonin gene-related peptide.

作者信息

Umeda Y, Takamiya M, Yoshizaki H, Arisawa M

机构信息

Department of Chemotherapy and Biochemistry, Nippon Roche Research Center, Kamakura, Japan.

出版信息

Biochem Biophys Res Commun. 1988 Jul 15;154(1):227-35. doi: 10.1016/0006-291x(88)90674-2.

Abstract

The effect of calcitonin gene-related peptide (CGRP) on mouse lymphocyte proliferation stimulated by mitogens was studied. CGRP (10(-10)-10(-7) M) dose-dependently inhibited the proliferative response of mouse lymph node cells and spleen cells stimulated by T cell mitogens concanavalin A (Con A) and phytohemagglutinin (PHA), whereas a B cell mitogen lipopolysaccharide (LPS) did not inhibit this response. The maximal inhibition by this peptide was 50% to 80% at 10(-8) and 10(-7) M. The addition of 10(-8) and 10(-7) M CGRP to lymph node cell cultures 24 hr after stimulation with Con A or PHA also had a significant inhibitory effect on the proliferative response. Furthermore, in the same concentration range (10(-10)-10(-7) M) CGRP increased intracellular cyclic AMP concentration in nylon wool nonadherent cells, but not in nylon wool adherent cells. CGRP had no significant effect on intracellular cyclic GMP concentration. In addition, specific binding of CGRP was observed in mouse spleen cells. Our present study suggests that CGRP inhibits the proliferative response of T lymphocytes to the mitogens by interacting with cell receptors coupled with adenylate cyclase. CGRP may be implicated in the regulation of T cell function.

摘要

研究了降钙素基因相关肽(CGRP)对丝裂原刺激的小鼠淋巴细胞增殖的影响。CGRP(10^-10 - 10^-7 M)剂量依赖性地抑制了由T细胞丝裂原刀豆球蛋白A(Con A)和植物血凝素(PHA)刺激的小鼠淋巴结细胞和脾细胞的增殖反应,而B细胞丝裂原脂多糖(LPS)并未抑制这种反应。该肽在10^-8和10^-7 M时的最大抑制率为50%至80%。在用Con A或PHA刺激24小时后,向淋巴结细胞培养物中添加10^-8和10^-7 M的CGRP也对增殖反应有显著的抑制作用。此外,在相同浓度范围(10^-10 - 10^-7 M)内,CGRP增加了尼龙毛非黏附细胞内的环磷酸腺苷(cAMP)浓度,但在尼龙毛黏附细胞中未增加。CGRP对细胞内环磷酸鸟苷(cGMP)浓度没有显著影响。此外,在小鼠脾细胞中观察到了CGRP的特异性结合。我们目前的研究表明,CGRP通过与与腺苷酸环化酶偶联的细胞受体相互作用,抑制T淋巴细胞对丝裂原的增殖反应。CGRP可能参与T细胞功能的调节。

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