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Regulation of Human Adipocyte Gene Expression by Thyroid Hormone
Author(s) -
Nathalie Viguerie,
L. Millet,
Sebastien Avizou,
Hubert Vidal,
Dominique Larrouy,
Dominique Langin
Publication year - 2002
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jcem.87.2.8200
Subject(s) - medicine , endocrinology , adipose tissue , biology , adipocyte , gene expression , lipolysis , regulation of gene expression , receptor , thyroid hormone receptor alpha , hormone , gene , transcription factor , nuclear receptor , biochemistry
Thyroid hormones are key regulators of metabolism. In adipose tissue, changes in thyroid status result in alterations of lipolytic capacity. The effects of these hormones are mediated by thyroid hormone receptors that modulate gene transcription. Very few target genes have been identified in adipose tissue. To investigate the effect of T(3) on gene expression in human adipocytes, primary cultures of human sc adipose tissue explants were treated with T(3). (32)P-labeled cDNA probes prepared from isolated adipocyte total RNA were hybridized to cDNA arrays representing 1,176 genes. Among the statistically significant variations in mRNA levels with more than 1.3-fold difference, 13 and 6 genes were positively and negatively regulated, respectively (n = 3). The genes encoded proteins that were involved in signal transduction, lipid metabolism, apoptosis, and inflammatory response. Using RT-competitive PCR, we showed a down-regulation of phosphodiesterase 3B, alpha(2A)-adrenergic receptor, and G protein alpha(i2) subunit mRNAs, and an up-regulation of beta(2)-adrenergic receptor mRNA. These regulations may explain the T(3)-mediated increase in catecholamine-induced lipolysis. The down-regulation of sterol regulatory element binding protein-1c, a transcription factor controlling lipogenic gene expression, may constitute a link between thyrotoxicosis and insulin resistance. Thus, these data suggest that T(3) modulates expression of genes with a wide range of function in human adipose tissue.

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