
Multifunctional gut iga+ plasma cells
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Access through your institution Buy or subscribe Nitric oxide, produced by iNOS, is required for IgA class-switch recombination in the small-intestinal lamina propria of mice. While
investigating the role of iNOS in the gut, the authors found a population of iNOS+ cells in intestinal lamina propria preparations from wild-type mice that was absent in mice lacking B
cells. Further examination of these iNOS+ cells showed that they expressed IgA and had undergone class-switch recombination, suggesting that these particular iNOS+ cells are a unique subset
of IgA+ plasma cells. Interestingly, these cells also produced TNF and expressed LY6C and LY6G, features usually associated with monocytic cells. Not all IgA+ cells expressed iNOS and/or
TNF, but those that did had a different morphology and cellular IgA localization compared with IgA+iNOS−TNF− cells, suggesting that some B cells in the gut adopt a more monocyte-like
phenotype as they differentiate into IgA+ plasma cells. But how are these cells induced? The authors found that the microbiota was necessary for the expression of iNOS by IgA+ cells, and
reconstitution of germ-free mice with a single bacterial species was sufficient for the induction of IgA+iNOS+ cells. Furthermore, only gut stroma from specific pathogen-free mice, and not
bone marrow-derived stroma or gut stroma from germ-free mice, could support the development of IgA+iNOS+ cells _in vitro_. This is a preview of subscription content, access via your
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* Learn about institutional subscriptions * Read our FAQs * Contact customer support ORIGINAL RESEARCH PAPER * Fritz, J. H. et al. Acquisition of a multifunctional IgA+ plasma cell phenotype
in the gut. _Nature_ 11 Dec 2011 (doi:10.1038/nature10698) Article Google Scholar Download references Authors * Olive Leavy View author publications You can also search for this author
inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Leavy, O. Multifunctional gut IgA+ plasma cells. _Nat Rev Immunol_ 12, 75 (2012).
https://doi.org/10.1038/nri3157 Download citation * Published: 13 January 2012 * Issue Date: February 2012 * DOI: https://doi.org/10.1038/nri3157 SHARE THIS ARTICLE Anyone you share the
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