Regulation of triglyceride metabolism by glucocorticoid receptor

被引:0
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作者
Jen-Chywan Wang
Nora E Gray
Taiyi Kuo
Charles A Harris
机构
[1] University of California at Berkeley,Department of Nutritional Science & Toxicology
[2] University of California,Graduate Program of Metabolic Biology
[3] University of California,Graduate Program of Endocrinology
[4] Gladstone Institute for Cardiovascular Disease,Department of Medicine
[5] University of California,undefined
来源
Cell & Bioscience | / 2卷
关键词
Glucocorticoid; Glucocorticoid receptor; Triglyceride; Lipogenesis; Lipolysis; Glucocorticoid response Element; Transcription;
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摘要
Glucocorticoids are steroid hormones that play critical and complex roles in the regulation of triglyceride (TG) homeostasis. Depending on physiological states, glucocorticoids can modulate both TG synthesis and hydrolysis. More intriguingly, glucocorticoids can concurrently affect these two processes in adipocytes. The metabolic effects of glucocorticoids are conferred by intracellular glucocorticoid receptors (GR). GR is a transcription factor that, upon binding to glucocorticoids, regulates the transcriptional rate of specific genes. These GR primary target genes further initiate the physiological and pathological responses of glucocorticoids. In this article, we overview glucocorticoid-regulated genes, especially those potential GR primary target genes, involved in glucocorticoid-regulated TG metabolism. We also discuss transcriptional regulators that could act with GR to participate in these processes. This knowledge is not only important for the fundamental understanding of steroid hormone actions, but also are essential for future therapeutic interventions against metabolic diseases associated with aberrant glucocorticoid signaling, such as insulin resistance, dyslipidemia, central obesity and hepatic steatosis.
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