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小鼠血小板生成素cDNA的克隆、表达及体内血小板生成的刺激

Cloning and expression of murine thrombopoietin cDNA and stimulation of platelet production in vivo.

作者信息

Lok S, Kaushansky K, Holly R D, Kuijper J L, Lofton-Day C E, Oort P J, Grant F J, Heipel M D, Burkhead S K, Kramer J M

机构信息

ZymoGenetics Corporation, Seattle, Washington 98105.

出版信息

Nature. 1994 Jun 16;369(6481):565-8. doi: 10.1038/369565a0.

Abstract

The major regulator of circulating platelet levels is believed to be a cytokine termed thrombopoietin. It is thought to be a lineage-specific cytokine affecting the proliferation and maturation of committed cells resulting in the production of megakaryocytes and platelets. Despite considerable efforts by a number of laboratories, the unequivocal identification of thrombopoietin has proven elusive. Here we report the functional cloning of a murine complementary DNA encoding a ligand for the receptor encoded by the c-mpl proto-oncogene (c-Mpl). The encoded polypeptide has a predicted molecular mass of 35,000 (M(r) 35K). The protein has a novel two-domain structure with an amino-terminal domain homologous with erythropoietin and a carboxy-terminal domain rich in serine, threonine and proline residues and containing seven potential N-linked glycosylation sites. Intraperitoneal injections of mice with recombinant protein increase circulating platelet levels by greater than fourfold after 7 days. These results along with those presented in the accompanying report strongly suggest that the ligand for c-Mpl is thrombopoietin.

摘要

循环血小板水平的主要调节因子被认为是一种名为血小板生成素的细胞因子。它被认为是一种谱系特异性细胞因子,影响定向细胞的增殖和成熟,从而导致巨核细胞和血小板的产生。尽管许多实验室付出了巨大努力,但血小板生成素的确切鉴定仍然难以捉摸。在此,我们报告了一种小鼠互补DNA的功能克隆,该DNA编码由c-mpl原癌基因(c-Mpl)编码的受体的配体。所编码的多肽预测分子量为35,000(M(r) 35K)。该蛋白具有一种新颖的双结构域结构,其氨基末端结构域与促红细胞生成素同源,羧基末端结构域富含丝氨酸、苏氨酸和脯氨酸残基,并含有七个潜在的N-连接糖基化位点。给小鼠腹腔注射重组蛋白7天后,循环血小板水平增加超过四倍。这些结果以及随附报告中呈现的结果强烈表明,c-Mpl的配体是血小板生成素。

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