Martin E R, Brenner B M, Ballermann B J
Renal Division, Brigham and Women's Hospital, Boston, Massachusetts 02115.
J Biol Chem. 1990 Aug 15;265(23):14044-9.
Two distinct cell surface endothelin receptors were identified, namely a 73-kDa protein referred to as ET-R1 and a 60-kDa protein named ET-R2. ET-R1 was expressed as the sole endothelin receptor on rat A10 vascular smooth muscle cells and C6 glial cells. Binding of 125I-ET-1 to these cells was inhibited by 50-200 pM endothelin-1 and -2, whereas endothelin-3 did not compete for this receptor subtype. Binding of 125I-ET-1 to intact A10 and C6 cells was reversible, indicating that ET-R1 is located on the cell surface. Affinity labelling of a single 73-kDa band on sodium dodecyl sulfate-polyacrylamide gels by 125I-ET-1 in A10 and C6 cells was inhibited by endothelin-1 but not by endothelin-3. In A10 cells, endothelin-1 but not endothelin-3 elicited a concentration-dependent increase in intracellular inositol trisphosphate levels. ET-R1 was also expressed in cultured rat glomerular mesangial cells based on findings of a subset of receptors with an apparent molecular mass of 73 kDa that bound 125I-ET-1 displacable by endothelin-1 and endothelin-2 but not by endothelin-3. These cells also expressed the ET-R2 receptor subtype, based on findings of a 60-kDa binding site that could be labeled by both 125I-ET-1 and 125I-ET-3. Labeling of ET-R2 by the radioactive endothelins-1 and -3 was inhibited competitively by endothelins-1, -2, and -3. Furthermore, ET-R2 was shown to be a functional receptor, as endothelin-3 caused inositol trisphosphate levels to rise in mesangial cells. An endothelin binding site with high affinity for endothelin-3 was also identified on rat PC12 pheochromocytoma cells, although the apparent molecular mass of this receptor could not be verified by cross-linking studies. Since endothelin-1 or -3 failed to augment inositol trisphosphate levels in these cells, this binding site could represent a third endothelin receptor subtype. Thus, two distinct functional receptors for endothelins were identified on rat cells, namely the 73-kDa ET-R1 which has an exceedingly low affinity for endothelin-3 and the 60-kDa ET-R2 which binds endothelin-3 with high affinity. Whether an additional endothelin receptor subtype exists in PC12 cells remains to be shown with certainty.
已鉴定出两种不同的细胞表面内皮素受体,即一种73 kDa的蛋白,称为ET-R1,以及一种60 kDa的蛋白,名为ET-R2。ET-R1作为大鼠A10血管平滑肌细胞和C6神经胶质细胞上唯一的内皮素受体而表达。125I-ET-1与这些细胞的结合可被50 - 200 pM的内皮素-1和-2抑制,而内皮素-3不与该受体亚型竞争。125I-ET-1与完整的A10和C6细胞的结合是可逆的,表明ET-R1位于细胞表面。在A10和C6细胞中,125I-ET-1对十二烷基硫酸钠 - 聚丙烯酰胺凝胶上单一73 kDa条带的亲和标记可被内皮素-1抑制,但不能被内皮素-3抑制。在A10细胞中,内皮素-1而非内皮素-3可引起细胞内三磷酸肌醇水平呈浓度依赖性升高。基于一组表观分子量为73 kDa的受体可结合125I-ET-1且可被内皮素-1和内皮素-2但不能被内皮素-3置换的研究结果,ET-R1也在培养的大鼠肾小球系膜细胞中表达。基于一个可被125I-ET-1和125I-ET-3标记的60 kDa结合位点的研究结果,这些细胞也表达ET-R2受体亚型。放射性内皮素-1和-3对ET-R2的标记可被内皮素-1、-2和-3竞争性抑制。此外,ET-R2被证明是一种功能性受体,因为内皮素-3可使系膜细胞中的三磷酸肌醇水平升高。在大鼠PC12嗜铬细胞瘤细胞上也鉴定出了一个对内皮素-3具有高亲和力的内皮素结合位点,尽管通过交联研究无法验证该受体的表观分子量。由于内皮素-1或-3未能提高这些细胞中的三磷酸肌醇水平,该结合位点可能代表第三种内皮素受体亚型。因此,在大鼠细胞上鉴定出了两种不同的内皮素功能性受体,即对内皮素-3亲和力极低的73 kDa的ET-R1和对内皮素-3具有高亲和力的60 kDa的ET-R2。PC12细胞中是否存在额外的内皮素受体亚型仍有待确切证实。