Cathepsins are required for Toll-like receptor 9 responses

F Matsumoto, S Saitoh, R Fukui, T Kobayashi… - Biochemical and …, 2008 - Elsevier
F Matsumoto, S Saitoh, R Fukui, T Kobayashi, N Tanimura, K Konno, Y Kusumoto…
Biochemical and biophysical research communications, 2008Elsevier
Toll-like receptors (TLR) recognize a variety of microbial products and activate defense
responses. Pathogen sensing by TLR2/4 requires accessory molecules, whereas little is
known about a molecule required for DNA recognition by TLR9. After endocytosis of
microbes, microbial DNA is exposed and recognized by TLR9 in lysosomes. We here show
that cathepsins, lysosomal cysteine proteases, are required for TLR9 responses. A cell line
Ba/F3 was found to be defective in TLR9 responses despite enforced TLR9 expression …
Toll-like receptors (TLR) recognize a variety of microbial products and activate defense responses. Pathogen sensing by TLR2/4 requires accessory molecules, whereas little is known about a molecule required for DNA recognition by TLR9. After endocytosis of microbes, microbial DNA is exposed and recognized by TLR9 in lysosomes. We here show that cathepsins, lysosomal cysteine proteases, are required for TLR9 responses. A cell line Ba/F3 was found to be defective in TLR9 responses despite enforced TLR9 expression. Functional cloning with Ba/F3 identified cathepsin B/L as a molecule required for TLR9 responses. The protease activity was essential for the complementing effect. TLR9 responses were also conferred by cathepsin S or F, but not by cathepsin H. TLR9-dependent B cell proliferation and CD86 upregulation were apparently downregulated by cathepsin B/L inhibitors. Cathepsin B inhibitor downregulated interaction of CpG-B with TLR9 in 293T cells. These results suggest roles for cathepsins in DNA recognition by TLR9.
Elsevier