TY - JOUR
T1 - Normal Development of the Gut-Associated Lymphoid Tissue Except Peyer's Patch in MyD88-Deficient Mice
AU - Iiyama, R.
AU - Kanai, T.
AU - Uraushihara, K.
AU - Ishikura, T.
AU - Makita, S.
AU - Totsuka, T.
AU - Yamazaki, M.
AU - Nakamura, T.
AU - Miyata, T.
AU - Yoshida, H.
AU - Takeuchi, O.
AU - Hoshino, K.
AU - Takeda, K.
AU - Ishikawa, H.
AU - Akirat, S.
AU - Watanabe, M.
N1 - Copyright:
Copyright 2012 Elsevier B.V., All rights reserved.
PY - 2003/12
Y1 - 2003/12
N2 - MyD88 is a key adaptor molecule for signalling via Toll-like receptors (TLRs) and the response to gut commensal microbes. To investigate the role of TLRs/MyD88 pathway in the development of the gut-associated lymphoid tissue (GALT), we examined the development of Peyer's patches (PPs) and cryptopatch (CP), and also one of effector compartment, intraepithelial lymphocyte (IEL) in MyD88 -/-, TLR2 -/- and TLR4 -/- mice. In MyD88 -/- mice, the organogenesis of PPs was not disturbed. However, PPs in 2-week-old MyD88 -/- mice were significantly smaller than those in MyD88 +/- mice. Also, in 2-week-old TLR4 -/-, but not TLR2 -/- mice, PPs did not develop rapidly. The development of PPs in MyD88 -/- and TLR4 -/- mice was completely recovered in 10 weeks. PP cells from MyD88 -/- mice showed significant decrease in proliferation when stimulated with lipopolysaccharide. The development of CP and IEL was also normal in 10-week-old MyD88 -/- mice. These results suggest that the TLRs/MyD88 pathway might be involved in the development of PPs only at early postnatal stage, and TLRs/MyD88-independent signalling is critically involved in the development of GALT in adult mice.
AB - MyD88 is a key adaptor molecule for signalling via Toll-like receptors (TLRs) and the response to gut commensal microbes. To investigate the role of TLRs/MyD88 pathway in the development of the gut-associated lymphoid tissue (GALT), we examined the development of Peyer's patches (PPs) and cryptopatch (CP), and also one of effector compartment, intraepithelial lymphocyte (IEL) in MyD88 -/-, TLR2 -/- and TLR4 -/- mice. In MyD88 -/- mice, the organogenesis of PPs was not disturbed. However, PPs in 2-week-old MyD88 -/- mice were significantly smaller than those in MyD88 +/- mice. Also, in 2-week-old TLR4 -/-, but not TLR2 -/- mice, PPs did not develop rapidly. The development of PPs in MyD88 -/- and TLR4 -/- mice was completely recovered in 10 weeks. PP cells from MyD88 -/- mice showed significant decrease in proliferation when stimulated with lipopolysaccharide. The development of CP and IEL was also normal in 10-week-old MyD88 -/- mice. These results suggest that the TLRs/MyD88 pathway might be involved in the development of PPs only at early postnatal stage, and TLRs/MyD88-independent signalling is critically involved in the development of GALT in adult mice.
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U2 - 10.1111/j.1365-3083.2003.01346.x
DO - 10.1111/j.1365-3083.2003.01346.x
M3 - Article
C2 - 14636418
AN - SCOPUS:0348014885
SN - 0300-9475
VL - 58
SP - 620
EP - 627
JO - Scandinavian Journal of Immunology
JF - Scandinavian Journal of Immunology
IS - 6
ER -