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牛白细胞介素4的表达及生物学活性:重组牛白细胞介素4对体外T细胞增殖及B细胞分化和增殖的影响

Expression and biological activities of bovine interleukin 4: effects of recombinant bovine interleukin 4 on T cell proliferation and B cell differentiation and proliferation in vitro.

作者信息

Estes D M, Hirano A, Heussler V T, Dobbelaere D A, Brown W C

机构信息

Department of Veterinary Microbiology, College of Veterinary Medicine, University of Missouri, Columbia 65211, USA.

出版信息

Cell Immunol. 1995 Jul;163(2):268-79. doi: 10.1006/cimm.1995.1126.

Abstract

Interleukin 4 (IL-4) is a pleotropic cytokine affecting a wide range of cell types in both the mouse and the human. These activities include regulation of the growth and differentiation of both T and B lymphocytes. The activities of IL-4 in nonprimate, nonmurine systems are not well established. Herein, we demonstrate in the bovine system that IL-4 upregulates production of IgM, IgG1, and IgE in the presence of a variety of costimulators including anti-IgM, Staphylococcus aureus cowan strain I, and pokeweed mitogen. IgE responses are potentiated by the addition of IL-2 to IL-4. Culture of bovine B lymphocytes with IL-4 in the absence of additional costimulators resulted in the increased surface expression of CD23 (low-affinity Fc epsilon RII), IgM, IL-2R, and MHC class II in a dose-dependent manner. IL-4 alone increased basal levels of proliferation of bulk peripheral blood mononuclear cells but in the presence of Con A inhibited proliferation. In contrast to the activities of IL-4 in the murine system, proliferation of TH1- and TH2-like clones was inhibited in a dose-dependent manner as assessed by antigen-or IL-2-driven in vitro proliferative responses. These observations are consistent with the role of IL-4 as a key player in regulation of both T and B cell responses.

摘要

白细胞介素4(IL-4)是一种多效性细胞因子,可影响小鼠和人类的多种细胞类型。这些活性包括调节T淋巴细胞和B淋巴细胞的生长与分化。IL-4在非灵长类、非鼠类系统中的活性尚未完全明确。在此,我们在牛系统中证明,在包括抗IgM、金黄色葡萄球菌考恩I株和商陆有丝分裂原在内的多种共刺激因子存在的情况下,IL-4可上调IgM、IgG1和IgE的产生。通过向IL-4中添加IL-2可增强IgE反应。在没有额外共刺激因子的情况下,用IL-4培养牛B淋巴细胞会导致CD23(低亲和力FcεRII)、IgM、IL-2R和MHC II类分子的表面表达呈剂量依赖性增加。单独的IL-4可增加外周血单个核细胞总体增殖的基础水平,但在有Con A存在的情况下会抑制增殖。与IL-4在鼠类系统中的活性相反,通过抗原或IL-2驱动的体外增殖反应评估,TH1样和TH2样克隆的增殖呈剂量依赖性受到抑制。这些观察结果与IL-4作为T细胞和B细胞反应调节中的关键参与者的作用一致。

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