EBM Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Watson, C. S.
Right arrow Articles by Gametchu, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Watson, C. S.
Right arrow Articles by Gametchu, B.
Experimental Biology and Medicine 228:1272-1281 (2003)
© 2003 Society for Experimental Biology and Medicine


MINIREVIEW

Proteins of Multiple Classes May Participate in Nongenomic Steroid Actions

Cheryl S. Watson*,1 and Bahiru Gametchu{dagger}

* Department of Human Biological Chemistry and Genetics, University of Texas, Medical Branch, Galveston, Texas 77555 and
{dagger} Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin 53226

Responses to steroids initiated from non-nuclear receptors impinge on a wide variety of cellular responses and utilize nearly all known signal transduction webs. While the mechanisms by which steroid receptors localize in the membrane are still unclear, it is apparent that this alternative localization allows steroid receptors to participate in a wide range of complex functions influencing cell proliferation, death, and differentiation. The central debate still remains the identity of the protein class or classes that mediate membrane-initiated (nongenomic) responses. The data thus far have supported several possibilities, including: nuclear steroid receptor-like forms in non-nuclear locations; other known (nonsteroid) membrane receptors or channels with additional steroid-binding sites; enzymes; transporters; receptors for serum steroid-binding proteins; unique and previously undescribed proteins; or chimeras of typical steroid receptor domains with other unique or known protein domains. Categorizing membrane steroid receptor proteins based exclusively on the actions of antagonists and agonists, without considering cell context and protein partnering issues, may mislead us into predicting more receptor subtypes than really exist. However, the plethora of signaling and functional outcomes may indicate the participation of more than one kind of steroid-binding protein. Resolving such unanswered questions will require future investigative focus on this alternative arm of steroid action, which is likely to yield as many therapeutic opportunities as have nuclear steroid mechanisms.

Key Words: protein partners • receptors • steroid-binding proteins • protein kinases • signaling • subcellular localization




This article has been cited by other articles:


Home page
FASEB J.Home page
C. S. Watson, Y.-J. Jeng, and M. Y. Kochukov
Nongenomic actions of estradiol compared with estrone and estriol in pituitary tumor cell signaling and proliferation
FASEB J, September 1, 2008; 22(9): 3328 - 3336.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
I. Nishimura, K. Ui-Tei, K. Saigo, H. Ishii, Y. Sakuma, and M. Kato
17{beta}-Estradiol at Physiological Concentrations Augments Ca2+-Activated K+ Currents via Estrogen Receptor {beta} in the Gonadotropin-Releasing Hormone Neuronal Cell Line GT1-7
Endocrinology, February 1, 2008; 149(2): 774 - 782.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
A. N. Bukiya, J. Liu, L. Toro, and A. M. Dopico
beta1 (KCNMB1) Subunits Mediate Lithocholate Activation of Large-Conductance Ca2+-Activated K+ Channels and Dilation in Small, Resistance-Size Arteries
Mol. Pharmacol., August 1, 2007; 72(2): 359 - 369.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
J. G. Greger, N. Fursov, N. Cooch, S. McLarney, L. P. Freedman, D. P. Edwards, and B. J. Cheskis
Phosphorylation of MNAR Promotes Estrogen Activation of Phosphatidylinositol 3-Kinase
Mol. Cell. Biol., March 1, 2007; 27(5): 1904 - 1913.
[Abstract] [Full Text] [PDF]


Home page
Eur Respir JHome page
G. Horvath and A. Wanner
Inhaled corticosteroids: effects on the airway vasculature in bronchial asthma
Eur. Respir. J., January 1, 2006; 27(1): 172 - 187.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
E.V. Younglai, Y.J. Wu, T.K. Kwan, and C.-Y. Kwan
Non-genomic action of estradiol and progesterone on cytosolic calcium concentrations in primary cultures of human granulosa-lutein cells
Hum. Reprod., September 1, 2005; 20(9): 2383 - 2390.
[Abstract] [Full Text] [PDF]


Home page
Mol. Endocrinol.Home page
C. Grossmann, A. Benesic, A. W. Krug, R. Freudinger, S. Mildenberger, B. Gassner, and M. Gekle
Human Mineralocorticoid Receptor Expression Renders Cells Responsive for Nongenotropic Aldosterone Actions
Mol. Endocrinol., July 1, 2005; 19(7): 1697 - 1710.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2003 by the Society for Experimental Biology and Medicine.