Suppr超能文献

鉴定ron基因产物作为人巨噬细胞刺激蛋白的受体。

Identification of the ron gene product as the receptor for the human macrophage stimulating protein.

作者信息

Wang M H, Ronsin C, Gesnel M C, Coupey L, Skeel A, Leonard E J, Breathnach R

机构信息

Immunopathology Section, National Cancer Institute, Frederick Cancer Research and Development Center, MD 21702.

出版信息

Science. 1994 Oct 7;266(5182):117-9. doi: 10.1126/science.7939629.

Abstract

Macrophage-stimulating protein (MSP) is a member of the hepatocyte growth factor-scatter factor (HGF-SF) family. Labeled MSP bound to Madin-Darby canine kidney (MDCK) cells transfected with complementary DNA encoding Ron, a cell membrane protein tyrosine kinase. Cross-linking of 125I-labeled MSP to transfected cells (MDCK-RE7 cells) and immunoprecipitation by antibodies to Ron revealed a 220-kilodalton complex, a size consistent with that of MSP (80 kilodaltons) cross-linked to the beta chain of Ron (150 kilodaltons). The binding of 125I-labeled MSP to MDCK-RE7 cells was inhibited by unlabeled MSP, but not by HGF-SF. MSP caused phosphorylation of the beta chain of Ron and induced migration of MDCK-RE7 cells. These results establish the ron gene product as a specific cell-surface receptor for MSP.

摘要

巨噬细胞刺激蛋白(MSP)是肝细胞生长因子-离散因子(HGF-SF)家族的成员。标记的MSP与用编码Ron(一种细胞膜蛋白酪氨酸激酶)的互补DNA转染的Madin-Darby犬肾(MDCK)细胞结合。将125I标记的MSP与转染细胞(MDCK-RE7细胞)交联,并通过抗Ron抗体进行免疫沉淀,发现了一个220千道尔顿的复合物,其大小与与Ron的β链(150千道尔顿)交联的MSP(80千道尔顿)一致。未标记的MSP可抑制125I标记的MSP与MDCK-RE7细胞的结合,但HGF-SF则不能。MSP导致Ron的β链磷酸化,并诱导MDCK-RE7细胞迁移。这些结果表明ron基因产物是MSP的特异性细胞表面受体。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验