Medical Hypotheses
Volume 73, Issue 5 , Pages 657-658, November 2009

Epigenetic programming of diverse glucocorticoid response and inflammatory/immune-mediated disease

  • Peisong Chen
  • ,
  • Tang Jiang

      Affiliations

    • Corresponding Author InformationCorresponding author. Address: Department of Laboratory Medicine, The First Affiliated Hospital of Sun Yat-Sen University, 58 Zhongshan Road II, Guangzhou, Guangdong, China. Tel.: +86 20 87330227; fax: +86 20 87750632.
  • ,
  • Juan Ouyang
  • ,
  • Yingpeng Cui
  • ,
  • Yili Chen

Department of Laboratory Medicine, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, China

Received 4 August 2009; accepted 9 August 2009. published online 02 September 2009.

Summary 

Glucocorticoid plays a fundamental role in maintaining immune homeostasis. Resistance to glucocorticoids is a potential etiology of inflammatory/immune-mediated disease. Most of the glucocorticoid effects are mediated by glucocorticoid receptor (GR), which has a complicated promoter region with multiple promoters. Studies have found that the methylation pattern of GR promoter is highly individual, which may contribute to the diverse glucocorticoid responds. Early life is a critical time for epigenetic programming of the body in which methylation imprints are established. Here we propose a hypothesis that connects the adverse early life events and the development of inflammatory/immune-mediated disease through an epigenetic mechanism, the methylation of GR gene.

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PII: S0306-9877(09)00563-5

doi:10.1016/j.mehy.2009.08.013

Medical Hypotheses
Volume 73, Issue 5 , Pages 657-658, November 2009