B cell-intrinsic MyD88 signaling prevents the lethal dissemination of commensal bacteria during colonic damage

Immunity. 2012 Feb 24;36(2):228-38. doi: 10.1016/j.immuni.2011.11.019. Epub 2012 Feb 1.

Abstract

The Toll-like receptor adaptor protein MyD88 is essential for the regulation of intestinal homeostasis in mammals. In this study, we determined that Myd88-deficient mice are susceptible to colonic damage that is induced by dextran sulfate sodium (DSS) administration resulting from uncontrolled dissemination of intestinal commensal bacteria. The DSS-induced mortality of Myd88-deficient mice was completely prevented by antibiotic treatment to deplete commensal bacteria. By using cell type-specific Myd88-deficient mice, we established that B cell-intrinsic MyD88 signaling plays a central role in the resistance to DSS-induced colonic damage via the production of IgM and complement-mediated control of intestinal bacteria. Our results indicate that the lack of intact MyD88 signaling in B cells, coupled with impaired epithelial integrity, enables commensal bacteria to function as highly pathogenic organisms, causing rapid host death.

Publication types

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

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism
  • Colon / drug effects
  • Colon / immunology*
  • Colon / injuries
  • Colon / microbiology*
  • Complement System Proteins / metabolism
  • Dextran Sulfate / toxicity
  • Host-Pathogen Interactions / immunology
  • Immunoglobulin A / metabolism
  • Immunoglobulin M / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myeloid Differentiation Factor 88 / deficiency
  • Myeloid Differentiation Factor 88 / genetics
  • Myeloid Differentiation Factor 88 / metabolism*
  • Signal Transduction

Substances

  • Anti-Bacterial Agents
  • Immunoglobulin A
  • Immunoglobulin M
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • Complement System Proteins
  • Dextran Sulfate