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Nat Immunol. 2008 Dec;9(12):1407-14. doi: 10.1038/ni.1669. Epub 2008 Oct 19.

Proteolytic cleavage in an endolysosomal compartment is required for activation of Toll-like receptor 9.

Author information

1
Whitehead Institute for Biomedical Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02115, USA.

Abstract

Toll-like receptors (TLRs) activate the innate immune system in response to pathogens. Here we show that TLR9 proteolytic cleavage is a prerequisite for TLR9 signaling. Inhibition of lysosomal proteolysis rendered TLR9 inactive. The carboxy-terminal fragment of TLR9 thus generated included a portion of the TLR9 ectodomain, as well as the transmembrane and cytoplasmic domains. This cleavage fragment bound to the TLR9 ligand CpG DNA and, when expressed in Tlr9(-/-) dendritic cells, restored CpG DNA-induced cytokine production. Although cathepsin L generated the requisite TLR9 cleavage products in a cell-free in vitro system, several proteases influenced TLR9 cleavage in intact cells. Lysosomal proteolysis thus contributes to innate immunity by facilitating specific cleavage of TLR9.

PMID:
18931679
PMCID:
PMC2735466
DOI:
10.1038/ni.1669
[Indexed for MEDLINE]
Free PMC Article

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