Abstract
Peyer's patches (PPs) and/or mesenteric lymph nodes (MLNs) are thought to be essential for immunoglobulin A (IgA) production. We found that the severe IgA deficiency in lymphotoxin-deficient (LT(-/-)) mice could be fully reversed by reconstitution with LT-expressing bone marrow, despite the absence of both LNs and PPs. The number of IgA precursors from LT(-/-) mice was not reduced, and they were able to migrate into the lamina propria (LP) of wild-type mice but not of LTbetaR(-/-) mice. Consistently, lymphoid tissue chemokines and adhesion molecules were reduced within the LP of LTalpha(-/-) and LTbetaR(-/-) mice. IgA deficiency in LTalpha(-/-) mice was reversed by the transplantation of a segment of RAG-1 (recombination-activating gene 1) deficient intestine, which confirmed the dispensability of the MLNs and PPs and the sufficiency of the LT-mediated gut microenvironment for IgA production.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adoptive Transfer
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Animals
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B-Lymphocyte Subsets / cytology
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B-Lymphocyte Subsets / immunology
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Cell Adhesion Molecules
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Chemokines / metabolism
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Chemotaxis, Leukocyte
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Female
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Homeodomain Proteins / genetics
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Homeodomain Proteins / metabolism
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Immunoglobulin A / biosynthesis*
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Immunoglobulins / metabolism
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Intestines / cytology
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Intestines / immunology*
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Intestines / transplantation
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Lymph Nodes / cytology
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Lymph Nodes / immunology
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Lymphotoxin beta Receptor
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Lymphotoxin-alpha / genetics
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Lymphotoxin-alpha / metabolism
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Mice
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Mice, Knockout
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Mucoproteins / metabolism
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Peyer's Patches / cytology
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Peyer's Patches / immunology
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Pregnancy
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Receptors, Tumor Necrosis Factor / deficiency
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Receptors, Tumor Necrosis Factor / genetics
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Receptors, Tumor Necrosis Factor / metabolism*
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Signal Transduction
Substances
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Cell Adhesion Molecules
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Chemokines
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Homeodomain Proteins
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Immunoglobulin A
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Immunoglobulins
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Ltbr protein, mouse
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Lymphotoxin beta Receptor
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Lymphotoxin-alpha
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Madcam1 protein, mouse
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Mucoproteins
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Receptors, Tumor Necrosis Factor
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RAG-1 protein