Affiliation:
1. Department of Cellular and Molecular Pharmacology, University of Illinois at Chicago, College of Medicine, 835 South Wolcott Avenue (MC 868), Chicago, Illinois 60612-7343
Abstract
ABSTRACT
The present study investigated G protein expression, localization, and functional coupling to thromboxane A
2
receptors (TPRs) during oligodendrocyte (OLG) development. It was found that as OLGs mature, the expression levels of G
q
increase while those of G
13
decrease. In contrast, the expression levels of G
s
, G
o
, and G
i
do not change significantly. Localization studies revealed that G
q
, G
13
, and G
i
are present only in the extranuclear compartment, whereas G
s
and G
o
are found in both the extranuclear and the nuclear compartments. Purification of TPR-G protein complexes demonstrated that TPRs couple to both G
q
and G
13
in the extranuclear compartment but only to G
s
in the nuclear compartment. Furthermore, functional analysis revealed that stimulation of nuclear TPR in OLGs stimulates CREB phosphorylation and myelin basic protein transcription and increases survival. Collectively, these results demonstrate that (i) OLGs selectively modulate the expression of certain G proteins during development, (ii) G proteins are differentially localized in OLGs leading to subcellular compartmentalization, (iii) TPRs couple to G
q
and G
13
in the extranuclear compartment and to G
s
only in the nucleus, (iv) mature OLGs have a functional nuclear TPR-G
s
signaling pathway, and (v) nuclear TPR signaling can stimulate CREB phosphorylation and myelin gene transcription and increase cell survival. These findings represent a novel paradigm for selective modulation of G protein-coupled receptor-G protein signaling during cell development.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
17 articles.
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