NATIVE-TYPE DHP-SENSITIVE CALCIUM-CHANNEL CURRENTS ARE PRODUCED BY CLONED RAT AORTIC SMOOTH-MUSCLE AND CARDIAC ALPHA-1 SUBUNITS EXPRESSED IN XENOPUS-LAEVIS OOCYTES AND ARE REGULATED BY ALPHA-2-SUBUNIT AND BETA-SUBUNIT

被引:36
作者
ITAGAKI, K
KOCH, WJ
BODI, I
KLOCKNER, U
SLISH, DF
SCHWARTZ, A
机构
[1] UNIV CINCINNATI,COLL MED,DEPT PHARMACOL & CELL BIOPHYS,231 BETHESDA AVE,CINCINNATI,OH 45267
[2] DUKE UNIV,MED CTR,HOWARD HUGHES MED INST,DURHAM,NC 27710
关键词
VOLTAGE-DEPENDENT CALCIUM CHANNEL; TISSUE-SPECIFIC SUBUNIT; COEXPRESSION; XENOPUS-LAEVIS OOCYTE;
D O I
10.1016/0014-5793(92)80542-O
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Native tissue-like L-type voltage-dependent calcium channels (L-VDCC's) were expressed by in vitro transcribed cRNA injection of rat aorta or rabbit cardiac alpha(1) subunit into Xenopus laevis oocytes. Co-injection of VSM-alpha(1) with the cloned skeletal muscle beta-subunit (SK-beta) of the L-type VDCC significantly increased the expressed peak current amplitude without significant changes in kinetics. Similar results were obtained by co-injection of cardiac alpha(1) (DSHT-alpha(1)) the cloned skeletal alpha(2)-subunit (SK-alpha(2)) or with SK-beta. The oocytes co-expressing cRNA's retained L-type VDCC pharmacology.
引用
收藏
页码:221 / 225
页数:5
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