G alpha(14) links a variety of G(i)- and G(s)-coupled receptors to the stimulation of phospholipase C

Citation
Mkc. Ho et al., G alpha(14) links a variety of G(i)- and G(s)-coupled receptors to the stimulation of phospholipase C, BR J PHARM, 132(7), 2001, pp. 1431-1440
Citations number
47
Categorie Soggetti
Pharmacology & Toxicology
Journal title
BRITISH JOURNAL OF PHARMACOLOGY
ISSN journal
00071188 → ACNP
Volume
132
Issue
7
Year of publication
2001
Pages
1431 - 1440
Database
ISI
SICI code
0007-1188(200104)132:7<1431:GALAVO>2.0.ZU;2-X
Abstract
1 The bovine G alpha (14) is a member of the G(q) subfamily of G proteins t hat can regulate phospholipase C beta isoforms but the extent to which G al pha (14) recognizes different receptor classes is not known. 2 G alpha (14) was cotransfected with a variety of receptors in COS-7 cells , and agonist-induced stimulation of phospholipase C was then measured. 3 Activation of the type 2 but not type 1 somatostatin receptor in cells co expressing G alpha (14) stimulated the accumulation of inositol phosphates; functional expression of both subtypes of somatostatin receptors was deter mined by the ability of somatostatin to inhibit cyclic AMP accumulation. 4 Among the three opioid receptors (mu, delta, and kappa), only the delta r eceptor was capable of stimulating IP formation when coexpressed with G alp ha (14) in COS-7 cells. 5 A panel of G(i)- and G(s)-linked receptors was screened for their ability to stimulate IP accumulation via G alpha (14). The adenosine A(1), complem ent C5a, dopamine D-1, D-2 and D-5, formyl peptide, luteinizing hormone, se cretin, and the three subtypes of melatonin (mt1, MT2, and Xenopus) recepto rs were all incapable of activating G alpha (14), while the alpha (2)- and Pz-adrenoceptors were able to do so. 6 G alpha (14)-mediated stimulation of phospholipase C beta was agonist dos e-dependent. These data demonstrate that although G alpha (14) can interact with different classes of receptors, it is much less promiscuous than G al pha (15) or G alpha (16).