Wang M H, Ronsin C, Gesnel M C, Coupey L, Skeel A, Leonard E J, Breathnach R
Immunopathology Section, National Cancer Institute, Frederick Cancer Research and Development Center, MD 21702.
Science. 1994 Oct 7;266(5182):117-9. doi: 10.1126/science.7939629.
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.
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。