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Hyporesponsiveness to glucocorticoids in mice genetically deficient for the corticosteroid binding globulin

Item Type:Article
Title:Hyporesponsiveness to glucocorticoids in mice genetically deficient for the corticosteroid binding globulin
Creators Name:Petersen, H.H. and Andreassen, T.K. and Breiderhoff, T. and Braesen, J.H. and Schulz, H. and Gross, V. and Groene, H.J. and Nykjaer, A. and Willnow, T.E.
Abstract:Corticosteroid binding globulin (CBG) is the carrier for glucocorticoids in plasma. The protein is believed to keep the steroids inactive and to regulate the amount of free hormone acting on target tissues (free hormone hypothesis). Here, we generated a mouse model genetically deficient for CBG to test the contribution of the carrier to glucocorticoid action and adrenocortical stress response. The absence of CBG resulted in a lack of corticosterone binding activity in serum and in an approximately 10-fold increase in free corticosterone levels in CBG-null mice, consistent with its role in regulation of circulating free hormone levels. Surprisingly, cbg(-)(/)(-) animals did not exhibit features seen in organisms with enhanced glucocorticoid signaling. Rather, the mice exhibited increased activity of the pituitary axis of hormonal control, normal levels of gluconeogenetic enzymes, and fatigue, as well as an aggravated response to septic shock, indicating an inability to appropriately respond to the excess free corticosterone in the absence of CBG. Thus, our data suggest an active role for CBG in bioavailability, local delivery, and/or cellular signal transduction of glucocorticoids that extends beyond a function as a mere cargo transporter.
Keywords:Adrenocorticotropic Hormone, Body Weight, Corticosterone, Exons, Food Deprivation, Gene Expression, Gene Targeting, Glucocorticoids, Inflammation, Intraperitoneal Injections, Kidney, Lipopolysaccharides, Liver, Survival Rate, Transcortin, Animals, Mice
Source:Molecular and Cellular Biology
ISSN:0270-7306
Publisher:American Society for Microbiology
Volume:26
Number:19
Page Range:7236-7245
Date:October 2006
Official Publication:https://doi.org/10.1128/MCB.00400-06
PubMed:View item in PubMed

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