Literature DB >> 8913370

Coupling efficiencies of human alpha 1-adrenergic receptor subtypes: titration of receptor density and responsiveness with inducible and repressible expression vectors.

T L Theroux1, T A Esbenshade, R D Peavy, K P Minneman.   

Abstract

We compared the efficiencies with which human alpha 1-adrenergic receptor (AR) subtypes activate inositol phosphate (InsP) formation and increase intracellular Ca2+ in transfected cell lines. Expression of human alpha 1a-, alpha 1b-, and alpha 1d-AR cDNAs under the repressible control of anhydrotetracycline in human embryonic kidney (HEK) 293 cells, which normally express no alpha 1-ARs, was used to compare responses to norepinephrine (NE) at different receptor densities. Maximal NE-stimulated InsP formation was found to increase with increasing density of each subtype, whereas basal levels and responses to sodium fluoride did not change. A comparison of multiple subclones over equivalent ranges of receptor expression showed that activation of each subtype resulted in different maximal responses (alpha 1a > alpha 1b > alpha 1d) in HEK 293 cells. Analogous studies were carried out in human SK-N-MC cells, which normally express low levels of all three alpha 1-AR subtypes, using an isopropyl-beta-D-thiogalactoside-inducible expression system. Induction with isopropyl-beta-D-thiogalactoside increased the density of individual alpha 1-AR subtypes by 4-6-fold over the level of endogenous expression. Increased expression of each of these subtypes in SK-N-MC cells did not alter the EC50 value for NE in stimulating InsP formation or releasing [Ca2+]i but did increase maximal responses to NE. Similar to our findings in HEK 293 cells, a comparison of responses at similar expression levels in SK-N-MC cells showed different maximal responses stimulated by each subtype, for both InsP (alpha 1a > alpha 1b > or = alpha 1d) and [Ca2+]i (alpha 1a > alpha 1b > alpha 1d) responses. These studies show that agonist-occupied human alpha 1-AR subtypes have different efficiencies in activating phospholipase C in human cell lines. In both HEK 293 and SK-N-MC cells, alpha 1a-ARs couple most efficiently, whereas alpha 1d-ARs couple very poorly.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8913370

Source DB:  PubMed          Journal:  Mol Pharmacol        ISSN: 0026-895X            Impact factor:   4.436


  21 in total

1.  Roles of the α1A-adrenergic receptor carboxyl tail in protein kinase C-induced phosphorylation and desensitization.

Authors:  Alejandro Cabrera-Wrooman; María Teresa Romero-Ávila; J Adolfo García-Sáinz
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2010-10-05       Impact factor: 3.000

2.  Targeting the cis-dimerization of LINGO-1 with low MW compounds affects its downstream signalling.

Authors:  L Cobret; M L De Tauzia; J Ferent; E Traiffort; I Hénaoui; F Godin; E Kellenberger; D Rognan; J Pantel; H Bénédetti; S Morisset-Lopez
Journal:  Br J Pharmacol       Date:  2014-12-15       Impact factor: 8.739

Review 3.  Phenotype pharmacology of lower urinary tract α(1)-adrenoceptors.

Authors:  A Nishimune; H Yoshiki; J Uwada; A S M Anisuzzaman; H Umada; I Muramatsu
Journal:  Br J Pharmacol       Date:  2012-03       Impact factor: 8.739

4.  Truncated isoforms inhibit [3H]prazosin binding and cellular trafficking of native human alpha1A-adrenoceptors.

Authors:  F Cogé; S P Guenin; A Renouard-Try; H Rique; C Ouvry; N Fabry; P Beauverger; J P Nicolas; J P Galizzi; J A Boutin; E Canet
Journal:  Biochem J       Date:  1999-10-01       Impact factor: 3.857

5.  Non-specific action of methoxamine on Ito, and the cloned channels hKv 1.5 and Kv 4.2.

Authors:  C Parker; Q Li; D Fedida
Journal:  Br J Pharmacol       Date:  1999-02       Impact factor: 8.739

6.  Microphysiometric analysis of human alpha1a-adrenoceptor expressed in Chinese hamster ovary cells.

Authors:  T Taniguchi; R Inagaki; S Murata; I Akiba; I Muramatsu
Journal:  Br J Pharmacol       Date:  1999-06       Impact factor: 8.739

7.  Differential modulation of α-1 adrenoceptor subtypes by antidepressants in the rat brain.

Authors:  D Ramakrishna; M N Subhash
Journal:  J Neural Transm (Vienna)       Date:  2010-12-07       Impact factor: 3.575

8.  Alpha(1D)-adrenergic receptor insensitivity is associated with alterations in its expression and distribution in cultured vascular myocytes.

Authors:  Lin-lin Fan; Shuang Ren; Hong Zhou; Ying Wang; Ping-xiang Xu; Jun-qi He; Da-li Luo
Journal:  Acta Pharmacol Sin       Date:  2009-12       Impact factor: 6.150

9.  Oxidative stress and alpha1-adrenoceptor-mediated stimulation of the Cl-/HCO3- exchanger in immortalized SHR proximal tubular epithelial cells.

Authors:  S Simão; S Fraga; P A Jose; P Soares-da-Silva
Journal:  Br J Pharmacol       Date:  2008-02-25       Impact factor: 8.739

10.  Functional characterization of alpha 1-adrenoceptor subtypes in vascular tissues using different experimental approaches: a comparative study.

Authors:  Regina Gisbert; Yolanda Madrero; Valentina Sabino; M Antonia Noguera; M Dolores Ivorra; Pilar D'Ocon
Journal:  Br J Pharmacol       Date:  2003-01       Impact factor: 8.739

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.