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PMID: 12421829 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Ubiquitination and proteasomal degradation of endogenous and exogenous inositol 1,4,5-trisphosphate receptors in alpha T3-1 anterior pituitary cells.

The Journal of biological chemistry ·Vol. 278 ·No. 2 ·2003-01-10 ·Pages 940-7

Wojcikiewicz RJ, Xu Q, Webster JM, Alzayady K, Gao C

Abstract

In alphaT3-1 mouse anterior pituitary gonadotropes, chronic activation of gonadotropin-releasing hormone (GnRH) receptors causes inositol 1,4,5-trisphosphate (InsP(3)) receptor down-regulation (Willars, G. B., Royall, J. E., Nahorski, S. R., El-Gehani, F., Everest, H. and McArdle, C. A. (2001) J. Biol. Chem. 276, 3123-3129). In the current study, we sought to define the mechanism behind this adaptive response. We show that GnRH induces a rapid and dramatic increase in InsP(3) receptor polyubiquitination and that proteasome inhibitors block InsP(3) receptor down-regulation and cause the accumulation of polyubiquitinated receptors. Thus, the ubiquitin/proteasome pathway is active in alphaT3-1 cells, and GnRH regulates the levels of InsP(3) receptors via this mechanism. Given these findings and further characterization of this system, we also examined the possibility that alphaT3-1 cells could be used to examine the ubiquitination of exogenous InsP(3) receptors introduced by cDNA transfection. This was found to be the case, since exogenous wild-type InsP(3) receptors, but not binding-defective mutant receptors, were polyubiquitinated in a GnRH-dependent manner, and agents that inhibited the polyubiquitination of endogenous receptors also inhibited the polyubiquitination of exogenous receptors. Further, we used this system to determine whether phosphorylation was involved in triggering InsP(3) receptor polyubiquitination. This was not the case, since mutation of serine residues 1588 and 1755 (the predominant phosphorylation sites in the type I receptor) did not inhibit polyubiquitination. In total, these data show that the ubiquitin/proteasome pathway is active in anterior pituitary cells, that this pathway targets both endogenous and exogenous InsP(3) receptors in GnRH-stimulated alphaT3-1 cells, and that, in contrast to the situation for many other substrates, phosphorylation does not trigger InsP(3) receptor polyubiquitination.

MeSH Terms
Animals Calcium Channels/metabolism Cysteine Endopeptidases/physiology Ethylenediamines/pharmacology Glycerol/pharmacology Gonadotropin-Releasing Hormone/pharmacology Inositol 1,4,5-Trisphosphate Receptors Mice Multienzyme Complexes/physiology Phosphorylation Pituitary Gland, Anterior/metabolism Proteasome Endopeptidase Complex Receptors, Cytoplasmic and Nuclear/metabolism Thapsigargin/pharmacology Transfection Ubiquitin/metabolism
Chemicals
Calcium Channels Ethylenediamines Inositol 1,4,5-Trisphosphate Receptors Multienzyme Complexes Receptors, Cytoplasmic and Nuclear Ubiquitin Gonadotropin-Releasing Hormone Thapsigargin Cysteine Endopeptidases Proteasome Endopeptidase Complex Glycerol N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Wojcikiewicz Richard J H
Department of Pharmacology, State University of New York Upstate Medical University, Syracuse 13210-2339, USA. [email protected]
Xu Qun
Webster Jack M
Alzayady Kamil
Gao Chen
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2003-01-10
Epub
2002-00-05
Pages
940-7
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIDDK NIH HHS · 5R01DK49194 · United States
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