Microenvironment regulates antibody secretion by IgA+ plasma cells.
نویسندگان
چکیده
Abstract IgA secreting plasma cells (PCs) provide a critical supply of antibodies for barrier functions against pathogens. These express unique tissue-driven transcriptional profiles in their respective niches the bone marrow (BM) and gut. We previously demonstrated that both tissues sustain long-lived IgA+ PCs, but cell intrinsic extrinsic signals responsible survival function gut remain largely unknown. Understanding how microenvironment regulates tissue resident PC has implications maintaining intestinal homeostasis protection from disease. found BM PCs functionally differ as they secrete significantly more antibody. To assess if this phenotype could be due to metabolic consequences, we profiled tissues. have similar glucose fatty acid uptake. However, increased mitochondrial dependence, while glycolytic capacity. next altered composition microbiome determine role microbes regulating PCs. Our initial experiments used C57BL/6J mice with well-defined low-complexity (from Jackson Labs). Co-housing Jax animals containing diverse set led an increase antibody secretion. Herein, identified influences function. aim dissect mechanisms involved driven changes phenotype. Ultimately, understanding intensity secretion provides tool targeting induction systemic mucosal responses will improve vaccine design development. Supported by grants NIH (R35 GM147560, R03 AI156481)
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ژورنال
عنوان ژورنال: Journal of Immunology
سال: 2023
ISSN: ['1550-6606', '0022-1767']
DOI: https://doi.org/10.4049/jimmunol.210.supp.218.03