INDUCIBLE EXPRESSION OF ALPHA(1B)-ADRENOCEPTORS IN DDT1 MF-2 CELLS - COMPARISON OF RECEPTOR DENSITY AND RESPONSE

被引:19
作者
ESBENSHADE, TA
WANG, XF
WILLIAMS, NG
MINNEMAN, KP
机构
[1] Department of Pharmacology, Emory University School of Medicine, Atlanta
来源
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION | 1995年 / 289卷 / 02期
关键词
ADRENOCEPTOR; NOREPINEPHRINE; INOSITOL PHOSPHATE; RECEPTOR RESERVE; SPARE RECEPTOR;
D O I
10.1016/0922-4106(95)90108-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hamster DDT1 MF-2 smooth muscle cells natively express alpha(1B)-adrenoceptors which are linked to phosphatidylinositol hydrolysis. We studied the relationship between alpha(1B)-adrenoceptor density and response in this cell line by stable transfection with an isopropyl-beta-D-thiogalactoside (IPTG)-inducible vector (pOP alpha(1B)) containing the hamster alpha(1B)-adrenoceptor cDNA. Transfected cells showed a 2-fold increase in receptor density compared to untransfected cells due to constitutive activity of the uninduced vector. Induction of vector expression caused a time-dependent increase in receptor density, reaching a maximum 8-fold increase after 48 h. Exposure to different concentrations of inducing agent for 16 h caused a graded increase in both receptor density and norepinephrine-stimulated [H-3]inositol phosphate (InsP) formation. A linear correlation between receptor density and maximum InsP response was observed. Induction of receptor expression did not alter the potency of norepinephrine in stimulating [H-3]InsP formation, suggesting that there was no receptor reserve, even at very high expression levels. This inducible expression system should be useful for relating receptor density and responsiveness, and comparing the coupling efficiency of closely related subtypes in activating different signal transduction mechanisms.
引用
收藏
页码:305 / 310
页数:6
相关论文
共 20 条
[1]  
CORNETT LE, 1982, J BIOL CHEM, V257, P694
[2]   MOLECULAR-CLONING AND EXPRESSION OF THE CDNA FOR THE HAMSTER ALPHA-1-ADRENERGIC RECEPTOR [J].
COTECCHIA, S ;
SCHWINN, DA ;
RANDALL, RR ;
LEFKOWITZ, RJ ;
CARON, MG ;
KOBILKA, BK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (19) :7159-7163
[3]  
DUCOEUR LC, 1992, STRATEGIES, V5, P70
[4]   [BE-2254-I-125, A NEW HIGH-AFFINITY RADIOLIGAND FOR ALPHA-1-ADRENOCEPTORS [J].
ENGEL, G ;
HOYER, D .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1981, 73 (2-3) :221-224
[5]  
ESBENSHADE TA, 1993, MOL PHARMACOL, V44, P76
[6]  
ESBENSHADE TA, 1994, ANN REV PHARM TOXICO, V34, P117
[7]  
ESBENSHADETA, 1994, MOL PHARMACOL, V45, P591
[8]  
FURCHGOTT RF, 1968, ANN NY ACAD SCI, V144, P882
[9]   ALPHA-1-ADRENOCEPTOR SUBTYPES LINKED TO DIFFERENT MECHANISMS FOR INCREASING INTRACELLULAR CA-2+ IN SMOOTH-MUSCLE [J].
HAN, C ;
ABEL, PW ;
MINNEMAN, KP .
NATURE, 1987, 329 (6137) :333-335
[10]   SUBTYPES OF ALPHA-1-ADRENOCEPTORS IN DDT1 MF-2 AND BC3H-1 CLONAL CELL-LINES [J].
HAN, C ;
ESBENSHADE, TA ;
MINNEMAN, KP .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1992, 226 (02) :141-148