Shraga-Levine Z, Galron R, Sokolovsky M
Laboratory of Neurobiochemistry, George S. Wise Faculty of Life Sciences, Tel Aviv University, Israel.
Biochemistry. 1994 Dec 13;33(49):14656-9. doi: 10.1021/bi00253a002.
Involvement of a cyclic GMP pathway in signal transduction stimulated by endothelins (ETs) and sarafotoxins (SRTXs) was explored using rat cerebellar slices. These peptides activated the same receptor binding sites (ET-1 and SRTX-b at the picomolar sites; ET-3 and SRTX-c at the nanomolar sites) to produce cyclic GMP, but their signaling pathways differed. The endothelins (ET-1 and ET-3) were found to signal via nitric oxide formation and to involve pertussis toxin-sensitive G-protein(s). The SRTXs (b and c), while also stimulating cyclic GMP production, did so via a pathway which is not L-arginine-dependent, i.e., carbon monoxide formation, and did not involve pertussis-toxin-sensitive G-protein(s). This is the first demonstration that the signaling pathways of endothelins and sarafotoxins may differ, even though they share the same binding sites.
利用大鼠小脑切片研究了环鸟苷酸途径在内皮素(ETs)和沙罗毒素(SRTXs)刺激的信号转导中的作用。这些肽激活相同的受体结合位点(皮摩尔位点的ET-1和SRTX-b;纳摩尔位点的ET-3和SRTX-c)以产生环鸟苷酸,但它们的信号通路不同。发现内皮素(ET-1和ET-3)通过一氧化氮形成进行信号传导,并涉及百日咳毒素敏感的G蛋白。沙罗毒素(b和c)虽然也刺激环鸟苷酸的产生,但其通过不依赖L-精氨酸的途径,即一氧化碳形成来实现,且不涉及百日咳毒素敏感的G蛋白。这是首次证明内皮素和沙罗毒素的信号通路可能不同,尽管它们共享相同的结合位点。