Lymphotoxin and TNF Produced by B Cells Are Dispensable for Maintenance of the Follicle-Associated Epithelium but Are Required for Development of Lymphoid Follicles in the Peyer’s Patches
Author(s) -
Alexei V. Tumanov,
Dmitry V. Kuprash,
Julie A. Mach,
Sergei A. Nedospasov,
Alexander V. Chervonsky
Publication year - 2004
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.173.1.86
Subject(s) - lymphotoxin , biology , microbiology and biotechnology , peyer's patch , b cell , tumor necrosis factor alpha , epithelium , lymphotoxin beta receptor , follicular dendritic cells , immunology , t cell , lymphatic system , antibody , antigen presenting cell , immune system , genetics
Organogenesis of Peyer's patches (PP), follicle-associated epithelium, and M cells is impaired in mice lacking B cells. At the same time, lymphotoxin (LT) and TNF are known to be critical for the development of PP. To directly address the function of LT and TNF expressed by B cells in the maintenance of PP structure, we studied the de novo formation of PP in B cell-deficient mice after the transfer of bone marrow from mice with targeted mutations in LT, TNF, or their combinations. We found that although the compartmentalization of T and B cell zones and development of follicular dendritic cells were affected by the lack of B cell-derived LT and TNF, the development of follicle-associated epithelium and M cells in PP was completely independent of LT/TNF production by B cells.
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