Transcriptional Control of Monocyte Gene Expression in Post-Traumatic Stress Disorder

Abstract

Post-traumatic stress disorder (PTSD) confers an increased risk for disorders with an inflammatory etiology. PTSD-related dysregulation of the sympathetic nervous system (SNS) and hypothalamic-pituitary adrenal (HPA) axis and associated alterations in inflammatory activity may contribute to this increased risk. However, little is known about convergent SNS, HPA and inflammatory signaling at the level of the immune cell transcriptome in PTSD. To explore such signaling, we examined the prevalence of specific transcription factor binding motifs in the promoter regions of differentially expressed genes in monocytes from individuals with PTSD and matched controls. Participants included 49 men (24 PTSD+ and 25 trauma-exposed controls) and 18 women (10 PTSD+ and 8 controls). Men with PTSD showed up-regulation of target genes for the NF-κB/Rel family of transcription factors, which convey inflammatory signals, up-regulation of target genes for CREB/ATF transcription factors, which convey adrenergic signals from the SNS, and down-regulation of target genes for the glucocorticoid receptor, which conveys glucocorticoid signals from the HPA axis. Women with PTSD also showed significant up-regulation of target genes for NF-κB and non-significant down-regulation of target genes for GR, but significant down-regulation of target genes for CREB/ATF. Altered transcriptional control of monocyte gene expression could contribute to exaggerated inflammatory activity in PTSD.

Document Details

Document Type
Pub Defense Publication
Publication Date
Jan 01, 2011
Source ID
10.1155/2011/560572

Entities

People

  • Aoife O'donovan
  • Bing Sun
  • Hans Rempel
  • Lynn Pulliam
  • Maryann Lenoci
  • Stephen Cole
  • Thomas Neylan

Organizations

  • Northern California Institute for Research and Education
  • United States Department of Defense
  • University of California
  • University of California, Los Angeles
  • University of California, San Francisco
  • Veterans Health Administration

Tags

Readers

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