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* The Jackson Laboratory, Bar Harbor, ME 04609;
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia; and
Basic Research Program, SAIC Frederick, Inc. and Laboratory of Molecular Immunoregulation, Center for Cancer Research, National Cancer Institute, Frederick. MD 21702
Organogenesis of Peyers 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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