دورية أكاديمية

CD137 is required for M cell functional maturation but not lineage commitment.

التفاصيل البيبلوغرافية
العنوان: CD137 is required for M cell functional maturation but not lineage commitment.
المؤلفون: Hsieh EH; Division of Biomedical Sciences, University of California, Riverside, Riverside, CA 92521, USA., Fernandez X, Wang J, Hamer M, Calvillo S, Croft M, Kwon BS, Lo DD
المصدر: The American journal of pathology [Am J Pathol] 2010 Aug; Vol. 177 (2), pp. 666-76. Date of Electronic Publication: 2010 Jul 08.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 0370502 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-2191 (Electronic) Linking ISSN: 00029440 NLM ISO Abbreviation: Am J Pathol Subsets: MEDLINE
أسماء مطبوعة: Publication: 2011-: New York : Elsevier
Original Publication: Philadelphia [etc.] American Assn. of Pathologists [etc.]
مواضيع طبية MeSH: Cell Lineage*, Lymphoid Tissue/*cytology , Peyer's Patches/*cytology , Tumor Necrosis Factor Receptor Superfamily, Member 9/*immunology, Animals ; B-Lymphocytes/cytology ; B-Lymphocytes/immunology ; Caco-2 Cells ; Cell Differentiation/immunology ; Cell Line ; Dendritic Cells/cytology ; Dendritic Cells/immunology ; Humans ; Intestinal Mucosa/cytology ; Lymphoid Tissue/immunology ; Mice ; Mice, Inbred BALB C ; Mice, Knockout ; Nasopharynx/anatomy & histology ; Peyer's Patches/immunology ; Tumor Necrosis Factor Receptor Superfamily, Member 9/genetics ; Tumor Necrosis Factor-alpha/immunology
مستخلص: Mucosal immune surveillance depends on M cells that reside in the epithelium overlying Peyer's patch and nasopharyngeal associated lymphoid tissue to transport particles to underlying lymphocytes. M cell development is associated with B lymphocytes in a basolateral pocket, but the interactions between these cells are poorly understood. In a cell culture model of M cell differentiation, we found lymphotoxin/tumor necrosis factor alpha induction of CD137 (TNFRSF9) protein on intestinal epithelial cell lines, raising the possibility that CD137 on M cells in vivo might interact with CD137L expressed by B cells. Accordingly, while CD137-deficient mice produced UEA-1+ M cell progenitors in nasopharyngeal associated lymphoid tissue and Peyer's patch epithelium, they showed an abnormal morphology, including the absence of basolateral B cell pockets. More important, CD137-deficient nasopharyngeal associated lymphoid tissue M cells were defective in microparticle transcytosis. Bone marrow irradiation chimeras confirmed that while induction of UEA-1+ putative M cell precursors was not CD137-dependent, full M cell transcytosis function required expression of CD137 by radioresistant stromal cells as well as by bone marrow-derived cells. These results are consistent with a two-step model of M cell differentiation, with initial CD137-independent commitment to the M cell lineage followed by a CD137-CD137L interaction of M cells with CD137-activated B lymphocytes or dendritic cells for functional maturation.
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معلومات مُعتمدة: R21 AI073689 United States AI NIAID NIH HHS; AI63426 United States AI NIAID NIH HHS; R01 AI042944 United States AI NIAID NIH HHS; AI42944 United States AI NIAID NIH HHS; AI73689 United States AI NIAID NIH HHS; P01 AI089624 United States AI NIAID NIH HHS; R01 AI063426 United States AI NIAID NIH HHS
المشرفين على المادة: 0 (Tumor Necrosis Factor Receptor Superfamily, Member 9)
0 (Tumor Necrosis Factor-alpha)
تواريخ الأحداث: Date Created: 20100710 Date Completed: 20110125 Latest Revision: 20220316
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC2913358
DOI: 10.2353/ajpath.2010.090811
PMID: 20616340
قاعدة البيانات: MEDLINE
الوصف
تدمد:1525-2191
DOI:10.2353/ajpath.2010.090811