Requirement for a conserved Toll/interleukin-1 resistance domain protein in the Caenorhabditis elegans immune response
Requirement for a conserved Toll/interleukin-1 resistance domain protein in the Caenorhabditis elegans immune response
The p38 mitogen-activated protein kinase pathway regulates innate immune responses in evolutionarily diverse species. We have previously shown that the Caenorhabditis elegans p38 mitogen-activated protein kinase, PMK-1, functions in an innate immune response pathway that mediates resistance to a variety of microbial pathogens. Here, we show that tir-1, a gene encoding a highly conserved Toll/IL-1 resistance (TIR) domain protein, is also required for C. elegans resistance to microbial pathogens. RNA interference inactivation of tir-1 resulted in enhanced susceptibility to killing by pathogens and correspondingly diminished PMK-1 phosphorylation. Unlike all known TIR-domain adapter proteins, overexpression of the human TIR-1 homologue, SARM, in mammalian cells was not sufficient to induce expression of NF-κB or IRF3-dependent reporter genes that are activated by Toll-like receptor signaling. These data reveal the involvement of a previously uncharacterized, evolutionarily conserved TIR domain protein in innate immunity that is functionally distinct from other known TIR domain signaling adapters.
- Massachusetts General Hospital United States
- University of Massachusetts Medical School United States
- Harvard University United States
570, Membrane Glycoproteins, Base Sequence, 610, Receptors, Interleukin-1, p38 Mitogen-Activated Protein Kinases, Enzyme Activation, Gene Expression Regulation, Receptors, Animals, Mitogen-Activated Protein Kinases, Caenorhabditis elegans, Interleukin-1, Immunology and Infectious Disease, DNA Primers, Signal Transduction
570, Membrane Glycoproteins, Base Sequence, 610, Receptors, Interleukin-1, p38 Mitogen-Activated Protein Kinases, Enzyme Activation, Gene Expression Regulation, Receptors, Animals, Mitogen-Activated Protein Kinases, Caenorhabditis elegans, Interleukin-1, Immunology and Infectious Disease, DNA Primers, Signal Transduction
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