Inui T, James A F, Fujitani Y, Takimoto M, Okada T, Yamamura T, Urade Y
International Research Laboratories, Ciba-Geigy Japan, Takarazuka.
Am J Physiol. 1994 Feb;266(2 Pt 1):L113-24. doi: 10.1152/ajplung.1994.266.2.L113.
We investigated the distribution of endothelin A (ETA) and ETB receptors in single smooth muscle cells and their contribution to ET-induced contractions of guinea pig trachea. ETA and ETB receptors were detected in smooth muscle membranes (maximum binding capacities of 810 and 360 fmol/mg protein and dissociation constants of 38 and 5.1 pM for 125I-labeled ET-1 and 125I-ET-3, respectively) and visualized autoradiographically in primary cultured cells. ET-1 and ET-3 evoked concentration-dependent increases in intracellular Ca2+ concentration and smooth muscle tension. The half-maximally effective concentrations of ET-1 and ET-3 at inducing contractions were 1.9 and 2.7 nM, respectively. The Ca2+ responses showed tachyphylaxis to both ETs after stimulation with ET-1, but only to ET-3 after stimulation with ET-3. Consecutive applications of ET-3 and ET-1 (10 nM each) classified the cells into ETA dominant (approximately 30%) responding to only ET-1, ETB dominant (approximately 20%) responding to only ET-3, and ETA- and ETB-possessing (approximately 50%) cells responding to both. The ETA antagonist, 10 microM BQ-123, attenuated ET-1-induced contractions but did not affect the ET-3-induced contractions. The results indicate that both receptors coexist in a major population of smooth muscle cells and cooperate in mediating ET-1-induced contractions.
我们研究了内皮素A(ETA)和ETB受体在单个平滑肌细胞中的分布及其对豚鼠气管内皮素(ET)诱导收缩的作用。在平滑肌细胞膜中检测到ETA和ETB受体(125I标记的ET-1和125I-ET-3的最大结合容量分别为810和360 fmol/mg蛋白,解离常数分别为38和5.1 pM),并在原代培养细胞中通过放射自显影进行可视化。ET-1和ET-3引起细胞内Ca2+浓度和平滑肌张力的浓度依赖性增加。ET-1和ET-3诱导收缩的半数有效浓度分别为1.9和2.7 nM。在用ET-1刺激后,Ca2+反应对两种ET均表现出快速耐受,但在用ET-3刺激后仅对ET-3表现出快速耐受。连续应用ET-3和ET-1(各10 nM)将细胞分为仅对ET-1有反应的ETA主导型(约30%)、仅对ET-3有反应的ETB主导型(约20%)以及对两者均有反应的同时拥有ETA和ETB的细胞(约50%)。ETA拮抗剂10 microM BQ-123减弱了ET-1诱导的收缩,但不影响ET-3诱导的收缩。结果表明,两种受体共存于大多数平滑肌细胞中,并共同介导ET-1诱导的收缩。