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Zinc-alpha2-glycoprotein, a lipid mobilizing factor, is expressed and secreted by human (SGBS) adipocytes.
- Source :
-
FEBS letters [FEBS Lett] 2005 Jan 03; Vol. 579 (1), pp. 41-7. - Publication Year :
- 2005
-
Abstract
- Zinc-alpha2-glycoprotein (ZAG), a lipid mobilizing factor, is expressed in mouse adipose tissue and is markedly upregulated in mice with cancer cachexia. We have explored whether ZAG is expressed and secreted by human adipocytes, using SGBS cells, and examined the regulation of ZAG expression. ZAG mRNA was detected by RT-PCR in mature human adipocytes and in SGBS cells post-, but not pre-, differentiation to adipocytes. Relative ZAG mRNA levels increased rapidly after differentiation of SGBS cells, peaking at day 8 post-induction. ZAG protein was evident in differentiated adipocytes (by day 3) and also detected in the culture medium (by day 6) post-induction. The PPARgamma agonist rosiglitazone induced a 3-fold increase in ZAG mRNA level, while TNF-alpha led to a 4-fold decrease. Human adipocytes express and secrete ZAG, with ZAG expression being regulated particularly through TNF-alpha and the PPARgamma nuclear receptor. ZAG is a novel adipokine, which may be involved in the local regulation of adipose tissue function.
- Subjects :
- Adipocytes chemistry
Adiponectin
Adipose Tissue metabolism
Cell Culture Techniques
Cell Differentiation genetics
Dexamethasone pharmacology
Gene Expression drug effects
Gene Expression genetics
Gene Expression Regulation
Humans
Insulin pharmacology
Intercellular Signaling Peptides and Proteins genetics
Intercellular Signaling Peptides and Proteins metabolism
Interleukin-6 genetics
Interleukin-6 pharmacology
Lipopolysaccharides pharmacology
Norepinephrine pharmacology
PPAR gamma agonists
PPAR gamma physiology
Peptides genetics
RNA, Messenger analysis
RNA, Messenger metabolism
Rosiglitazone
Seminal Plasma Proteins genetics
Thiazolidinediones pharmacology
Tumor Necrosis Factor-alpha pharmacology
Tumor Necrosis Factor-alpha physiology
Zn-Alpha-2-Glycoprotein
Adipocytes metabolism
Peptides metabolism
Seminal Plasma Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0014-5793
- Volume :
- 579
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- FEBS letters
- Publication Type :
- Academic Journal
- Accession number :
- 15620688
- Full Text :
- https://doi.org/10.1016/j.febslet.2004.11.042