Functional differences between splice variants of the murine 5-MT3A receptor: possible role for phosphorylation

Citation
Pc. Hubbard et al., Functional differences between splice variants of the murine 5-MT3A receptor: possible role for phosphorylation, MOL BRAIN R, 81(1-2), 2000, pp. 101-108
Citations number
25
Categorie Soggetti
Neurosciences & Behavoir
Journal title
MOLECULAR BRAIN RESEARCH
ISSN journal
0169328X → ACNP
Volume
81
Issue
1-2
Year of publication
2000
Pages
101 - 108
Database
ISI
SICI code
0169-328X(20000930)81:1-2<101:FDBSVO>2.0.ZU;2-K
Abstract
The murine 5-HT3A receptor subunit is expressed as either of two splice var iants which are differentially regulated in vivo. The difference resides in a six-amino acid sequence within the cytoplasmic loop between transmembran e regions 3 and 4, which is present in the long form but not the short form . No physiological roles have yet been ascribed to the two splice variants. Whole cell patch clamp recording from transfected HEK 293 cells stably exp ressing either long or short form receptors showed very similar responses u nder control conditions. However, inclusion of 1 mM cAMP (activator of prot ein kinase A) in the patch pipette caused an initial increase in the desens itization rate of the long form, but a decrease in the short form. With the addition of 100 nM phorbol 12-myristate 13-acetate (PMA; activator of prot ein kinase C) to the pipette solution, responses elicited with 1 mu M 5-HT revealed an increase in the current amplitude in the long but not the short form of the receptor. Over a longer time period, inclusion of PMA in the p atch-pipette caused a faster run down of peak current amplitude in response to 30 mu M 5-HT in the long form but did not affect the short form; there was no observed long-term effects of cAMP. We conclude that the long and sh ort forms of the 5-HT, receptor are differentially modulated by agents that activate PKA and PKC. These different patterns of modulation could have ma rkedly divergent consequences on receptor function. (C) 2000 Elsevier Scien ce B.V. All rights reserved.