Regulation of triglyceride metabolism by glucocorticoid receptor

被引:0
|
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
关键词
Glucocorticoid; Glucocorticoid receptor; Triglyceride; Lipogenesis; Lipolysis; Glucocorticoid response Element; Transcription;
D O I
暂无
中图分类号
学科分类号
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.
引用
收藏
相关论文
共 50 条
  • [21] Regulation of Glucocorticoid Production by Nuclear Lipid Metabolism
    Sewer, Marion B.
    FASEB JOURNAL, 2013, 27
  • [22] Glucocorticoid Receptor Mediates Cortisol Regulation of Glycogen Metabolism in Gills of the Euryhaline Tilapia (Oreochromis mossambicus)
    Wu, Chien-Yu
    Lee, Tsung-Han
    Tseng, Deng-Yu
    FISHES, 2023, 8 (05)
  • [23] Role of caspase-1 in regulation of triglyceride metabolism
    Kotas, Maya E.
    Jurczak, Michael J.
    Annicelli, Charles
    Gillum, Matthew P.
    Cline, Gary W.
    Shulman, Gerald I.
    Medzhitov, Ruslan
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (12) : 4810 - 4815
  • [24] REGULATION OF HEPATIC TRIGLYCERIDE METABOLISM BY FREE FATTY ACIDS
    KOHOUT, M
    KOHOUTOVA, B
    HEIMBERG, M
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1971, 246 (16) : 5067 - +
  • [25] Defective regulation of triglyceride metabolism by insulin in the liver in NIDDM
    R. Malmström
    C. J. Packard
    M. Caslake
    D. Bedford
    P. Stewart
    H. Yki-Järvinen
    J. Shepherd
    M.-R. Taskinen
    Diabetologia, 1997, 40 : 454 - 462
  • [26] Defective regulation of triglyceride metabolism by insulin in the liver in NIDDM
    Malmstrom, R
    Packard, CJ
    Caslake, M
    Bedford, D
    Stewart, P
    YkiJarvinen, H
    Shepherd, J
    Taskinen, MR
    DIABETOLOGIA, 1997, 40 (04) : 454 - 462
  • [27] Regulation of triglyceride metabolism by Angiopoietin-like proteins
    Mattijssen, Frits
    Kersten, Sander
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2012, 1821 (05): : 782 - 789
  • [28] Expression of glucocorticoid receptor beta and its regulation in glucocorticoid responsiveness in glaucoma
    Yorio, T
    Clark, AF
    Zhang, X
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2004, 45 : U435 - U435
  • [29] Glucocorticoid down-regulation of rat glucocorticoid receptor does not involve differential promoter regulation
    Freeman, AI
    Munn, HL
    Lyons, V
    Dammermann, A
    Seckl, JR
    Chapman, KE
    JOURNAL OF ENDOCRINOLOGY, 2004, 183 (02) : 365 - 374
  • [30] GLUCOCORTICOID RECEPTOR REGULATION - BIOPOTENCY OF CORTICOSTERONE IN DOWN-REGULATION
    SVEC, F
    CLINICAL RESEARCH, 1983, 31 (05): : A870 - A870