Cross D, Cifuentes F, Huidobro-Toro J P, Vío C P, Inestrosa N C
Department of Cell Biology, Catholic University of Chile, Santiago.
Brain Res. 1987 Sep;388(3):268-70. doi: 10.1016/0169-328x(87)90034-9.
Xenopus laevis oocytes were injected with poly(A)+ mRNA isolated from rat brain and superfused in a medium containing either serotonin, angiotensin II or bradykinin. Applications of serotonin or angiotensin II to injected oocytes elicited, in a dose-dependent manner, changes in membrane potential. The angiotensin II receptor was desensitized fairly rapidly in the continued presence of the agonist. No response was obtained with bradykinin. The selectivity of the angiotensin II-induced response was demonstrated by the finding that the angiotensin II antagonist [( Sar1,Ala8]angiotensin II, saralasin) blocked the angiotensin II-induced response. It is concluded that an appropriate fraction of brain mRNA is capable of directing the synthesis and correct insertion of functional angiotensin II receptors in the Xenopus oocyte membrane.
将从大鼠脑中分离得到的多聚腺苷酸(poly(A)+)mRNA注射到非洲爪蟾卵母细胞中,并在含有5-羟色胺、血管紧张素II或缓激肽的培养基中进行灌流。向注射了mRNA的卵母细胞施加5-羟色胺或血管紧张素II会以剂量依赖的方式引起膜电位变化。在激动剂持续存在的情况下,血管紧张素II受体相当迅速地发生脱敏。缓激肽未引起反应。血管紧张素II拮抗剂[(Sar1,Ala8)血管紧张素II,沙拉新]可阻断血管紧张素II诱导的反应,这一发现证明了血管紧张素II诱导反应的选择性。结论是,脑mRNA的适当部分能够指导功能性血管紧张素II受体在非洲爪蟾卵母细胞膜中的合成和正确插入。