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补体C3的一种替代形式的结构,其对B淋巴细胞表现出共刺激生长因子活性。

The structure of an alternate form of complement C3 that displays costimulatory growth factor activity for B lymphocytes.

作者信息

Cahen-Kramer Y, Mårtensson I L, Melchers F

机构信息

Basel Institute for Immunology, Switzerland.

出版信息

J Exp Med. 1994 Dec 1;180(6):2079-88. doi: 10.1084/jem.180.6.2079.

Abstract

In this study, the structure of a novel 1.9-kb transcript coding for complement component 3 (C3) is described. This alternate C3 is identical to the 3' end of the C3 message beginning at position 3300 of the C3 cDNA. Its transcription appears to be driven by an alternate promoter located within intron 8 of the C3 gene. This alternate C3 message contains an open reading frame that may encode a 536-amino acid-long protein identical to the 3' part of the C3 alpha chain. The resulting protein contains the complement receptor CR2 binding site. The suggested 5' end of coding region of the alternate C3 includes information for a potential hydrophobic leader peptide that would allow secretion of the protein. In vitro assays with macrophage-depleted mouse splenic B cells indicate that an activity is secreted from cell lines transfected with the alternate C3 cDNA. Together with Sepharose-bound immunoglobulin M-specific monoclonal antibodies and interleukin 2, it costimulates the proliferation of B cells. Implications for possible in vivo functions are discussed.

摘要

在本研究中,描述了一种编码补体成分3(C3)的新型1.9 kb转录本的结构。这种替代性C3与C3 cDNA第3300位开始的C3信使RNA的3'末端相同。其转录似乎由位于C3基因第8内含子内的一个替代性启动子驱动。这种替代性C3信使RNA包含一个开放阅读框,可能编码一种与C3α链3'部分相同的536个氨基酸长的蛋白质。所产生的蛋白质包含补体受体CR2结合位点。替代性C3编码区的建议5'末端包含一个潜在疏水前导肽的信息,该前导肽可使蛋白质分泌。对巨噬细胞耗竭的小鼠脾B细胞进行的体外试验表明,用替代性C3 cDNA转染的细胞系可分泌一种活性物质。与琼脂糖凝胶结合的免疫球蛋白M特异性单克隆抗体和白细胞介素2一起,它可共刺激B细胞的增殖。文中讨论了其可能的体内功能。

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