Impaired CD4+ T-cell proliferation and effector function correlates with repressive histone methylation events in a mouse model of severe sepsis

Eur J Immunol. 2010 Apr;40(4):998-1010. doi: 10.1002/eji.200939739.

Abstract

Immunosuppression following severe sepsis remains a significant human health concern, as long-term morbidity and mortality rates of patients who have recovered from life-threatening septic shock remain poor. Mouse models of severe sepsis indicate this immunosuppression may be partly due to alterations in myeloid cell function; however, the effect of severe sepsis on subsequent CD4(+) T-cell responses remains unclear. In the present study, CD4(+) T cells from mice subjected to an experimental model of severe sepsis (cecal ligation and puncture (CLP)) were analyzed in vitro. CD4(+)CD62L(+) T cells from CLP mice exhibited reduced proliferative capacity and altered gene expression. Additionally, CD4(+)CD62L(+) T cells from CLP mice exhibit dysregulated cytokine production after in vitro skewing with exogenous cytokines, indicating a decreased capability of these cells to commit to either the T(H)1 or T(H)2 lineage. Repressive histone methylation marks were also evident at promoter regions for the T(H)1 cytokine IFN-gamma and the T(H)2 transcription factor GATA-3 in naïve CD4(+) T cells from CLP mice. These results provide evidence that CD4(+) T-cell subsets from post-septic mice exhibit defects in activation and effector function, possibly due to chromatin remodeling proximal to genes involved in cytokine production or gene transcription.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / pathology
  • Cells, Cultured / immunology
  • Chromatin Assembly and Disassembly / immunology
  • Female
  • GATA3 Transcription Factor / genetics
  • Gene Expression Regulation / immunology*
  • Histones / metabolism*
  • Interferon-gamma / genetics
  • Intestinal Perforation / complications
  • L-Selectin / immunology
  • Lymphocyte Activation / drug effects
  • Lymphocyte Activation / immunology*
  • Lymphocyte Subsets / immunology*
  • Lymphocyte Subsets / pathology
  • MAP Kinase Kinase 4 / metabolism
  • Methylation
  • Mice
  • Mice, Inbred C57BL
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Protein Processing, Post-Translational*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Receptors, CCR7 / biosynthesis
  • Receptors, CCR7 / immunology
  • Shock, Septic / genetics
  • Shock, Septic / immunology*
  • Specific Pathogen-Free Organisms

Substances

  • Ccr7 protein, mouse
  • GATA3 Transcription Factor
  • Gata3 protein, mouse
  • Histones
  • RNA, Messenger
  • Receptors, CCR7
  • L-Selectin
  • Interferon-gamma
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • MAP Kinase Kinase 4