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

机译:补体C3替代形式的结构对B淋巴细胞显示共刺激生长因子活性

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摘要

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.
机译:在这项研究中,描述了编码补体成分3(C3)的新型1.9-kb转录本的结构。此备用C3与C3消息的3'末端相同,起始于C3 cDNA的位置3300。它的转录似乎由位于C3基因内含子8内的另一个启动子驱动。此备用C3消息包含一个开放阅读框,该框可能编码与C3α链3'部分相同的536个氨基酸长的蛋白质。所得蛋白质包含补体受体CR2结合位点。建议的备用C3编码区的5'端包括潜在的疏水前导肽的信息,该肽可允许蛋白质分泌。用巨噬细胞耗竭的小鼠脾脏B细胞进行的体外测定表明,活性是从用其他C3 cDNA转染的细胞系中分泌的。与琼脂糖结合的免疫球蛋白M特异性单克隆抗体和白介素2一起,共同刺激了B细胞的增殖。讨论了可能的体内功能。

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