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源自补体成分C5的C5a片段的肿瘤细胞趋化因子。

Chemotactic factor for tumor cells derived from the C5a fragment of complement component C5.

作者信息

Orr W, Phan S H, Varani J, Ward P A, Kreutzer D L, Webster R O, Henson P M

出版信息

Proc Natl Acad Sci U S A. 1979 Apr;76(4):1986-9. doi: 10.1073/pnas.76.4.1986.

Abstract

Previously, we have stablished that the fifth component of complement (C5) serves as an important source of mediators that have locomotory (chemotactic) activity for leukocytes and tumor cells. C5a, a fragment (Mr 11,200) derived from the NH2-terminal portion of the alpha chain of C5, is the major chemotactic peptide for leukocytes. The present studies demonstrate that cleavage of C5a with trypsin generates a derivative peptide that is chemotactic for tumor cells (Walker carcinosarcoma). This fragment has an estimated Mr of 6000 as assessed by gel filtration and does not require the COOH-terminal arginine of C5a, because equivalent amounts of chemotactic activity for tumor cells can be generated from des-Arg-C5a by digestion with trypsin. The C5a-derived chemotactic peptide for tumor cells demonstrates peak activity at approximately 1 pM. These studies emphasize the key role of the C5a region of the C5 molecule in the generation of peptides that affect locomotory responses of cells.

摘要

此前,我们已经确定补体第五成分(C5)是具有趋化活性的介质的重要来源,这些介质对白细胞和肿瘤细胞具有趋化作用。C5a是一种源自C5α链氨基末端部分的片段(分子量11,200),是白细胞的主要趋化肽。目前的研究表明,用胰蛋白酶切割C5a可产生一种对肿瘤细胞(沃克癌肉瘤)具有趋化作用的衍生肽。通过凝胶过滤评估,该片段的估计分子量为6000,并且不需要C5a的羧基末端精氨酸,因为用胰蛋白酶消化des-Arg-C5a可产生等量的对肿瘤细胞的趋化活性。源自C5a的对肿瘤细胞具有趋化作用的肽在大约1 pM时表现出峰值活性。这些研究强调了C5分子的C5a区域在产生影响细胞趋化反应的肽中的关键作用。

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