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Cellular responses to bacterial cell wall components are mediated through MyD88-dependent signaling cascades.
Takeuchi, O; Takeda, K; Hoshino, K; Adachi, O; Ogawa, T; Akira, S.
Affiliation
  • Takeuchi O; Department of Host Defense, Research Institute for Microbial Diseases, Osaka University and CREST of Japan Science and Technology Corp., 3-1 Yamada-oka, Suita, Osaka 565-0871, Japan.
Int Immunol ; 12(1): 113-7, 2000 Jan.
Article in En | MEDLINE | ID: mdl-10607756
ABSTRACT
MyD88 is an adaptor molecule essential for signaling via the Toll-like receptor (TLR)/IL-1 receptor family. TLR4 is a member of the TLR family and a point mutation in the Tlr4 gene causes hyporesponsiveness to lipopolysaccharide (LPS) in C3H/HeJ mice. We have previously shown that both TLR4- and MyD88-deficient mice are hyporesponsive to LPS. In this study we examined the responsiveness of these two knockout mice to various bacterial cell wall components. Cells from TLR4-deficient mice responded to several kinds of LPS, peptidoglycan and crude cell wall preparation from Gram-positive bacteria and mycobacterial lysates. In contrast, macrophages and splenocytes from MyD88-deficient mice did not respond to any of the bacterial components we tested. These results show that MyD88 is essential for the cellular response to bacterial cell wall components.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Membrane Glycoproteins / Peptidoglycan / Receptors, Immunologic / Antigens, Differentiation / Cell Wall / Lipopolysaccharides / Receptors, Cell Surface / Drosophila Proteins Limits: Animals Language: En Journal: Int Immunol Journal subject: ALERGIA E IMUNOLOGIA Year: 2000 Document type: Article Affiliation country:
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Collection: 01-internacional Database: MEDLINE Main subject: Membrane Glycoproteins / Peptidoglycan / Receptors, Immunologic / Antigens, Differentiation / Cell Wall / Lipopolysaccharides / Receptors, Cell Surface / Drosophila Proteins Limits: Animals Language: En Journal: Int Immunol Journal subject: ALERGIA E IMUNOLOGIA Year: 2000 Document type: Article Affiliation country:
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