Two distinct lymphocyte homing systems involved in the pathogenesis of chronic inflammatory gastrointestinal diseases
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  • 作者:Motohiro Kobayashi (1)
    Hitomi Hoshino (12)
    Kenichi Suzawa (1)
    Yasuhiro Sakai (1)
    Jun Nakayama (1)
    Minoru Fukuda (3) minoru@sanfordburnham.org
  • 关键词:Gastrointestinal tract &#8211 ; Chronic inflammation &#8211 ; High endothelial venule (HEV) &#8211 ; Peripheral lymph node addressin (PNAd) &#8211 ; Mucosal addressin cell adhesion molecule 1 (MAdCAM ; 1)
  • 刊名:Seminars in Immunopathology
  • 出版年:2012
  • 出版时间:May 2012
  • 年:2012
  • 卷:34
  • 期:3
  • 页码:401-413
  • 全文大小:981.6 KB
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  • 作者单位:1. Department of Molecular Pathology, Shinshu University Graduate School of Medicine, 3-1-1 Asahi, Matsumoto, 390-8621 Japan2. Department of Alzheimer鈥檚 Disease Research, National Institute for Longevity Science, Obu, 474-8511 Japan3. Tumor Microenvironment Program, Cancer Research Center, Sanford-Burnham Medical Research Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Biomedicine
    Immunology
    Internal Medicine
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1863-2300
文摘
Under normal and pathological conditions, lymphocyte migration into the gastrointestinal mucosa to form gut-associated lymphoid tissue is mediated by the L-selectin ligand peripheral lymph node addressin and the integrin α4β7 ligand mucosal addressin cell adhesion molecule 1 (MAdCAM-1) expressed on high endothelial venules (HEVs) and HEV-like vessels. In this review, we discuss these two distinct lymphocyte homing systems involved in the pathogenesis of chronic inflammatory gastrointestinal diseases with reference to our and others’ previously published works. We also describe a recently developed recombinant integrin α4β7 heterodimeric IgG chimera that can be used as an immunohistochemical reagent to stain functional MAdCAM-1.

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