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Discrete populations of isotype-switched memory B lymphocytes are maintained in murine spleen and bone marrow

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Riedel,  René
Guest Group Evolutionary Genomics, Max Planck Institute for Evolutionary Biology, Max Planck Society;

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Schulz,  Daniel
Department of Molecular Biology, MPI for Biophysical Chemistry, Max Planck Society;

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Köhler,  Ralf
Optical and Interpretative Astronomy, MPI for Extraterrestrial Physics, Max Planck Society;

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Durek,  Pawel
BioinformaticsCIG, Infrastructure Groups and Service Units, Max Planck Institute of Molecular Plant Physiology, Max Planck Society;

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s41467-020-16464-6.pdf
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Citation

Riedel, R., Addo, R., Ferreira-Gomes, M., Heinz, G. A., Heinrich, F., Kummer, J., et al. (2020). Discrete populations of isotype-switched memory B lymphocytes are maintained in murine spleen and bone marrow. Nature Communications, 11: 2570. doi:10.1038/s41467-020-16464-6.


Cite as: https://hdl.handle.net/21.11116/0000-0009-4D29-4
Abstract
At present, it is not clear how memory B lymphocytes are maintained over time, and whether only as circulating cells or also residing in particular tissues. Here we describe distinct populations of isotype-switched memory B lymphocytes (Bsm) of murine spleen and bone marrow, identified according to individual transcriptional signature and B cell receptor repertoire. A population of marginal zone-like cells is located exclusively in the spleen, while a population of quiescent Bsm is found only in the bone marrow. Three further resident populations, present in spleen and bone marrow, represent transitional and follicular B cells and B1 cells, respectively. A population representing 10-20% of spleen and bone marrow memory B cells is the only one qualifying as circulating. In the bone marrow, all cells individually dock onto VCAM1+ stromal cells and, reminiscent of resident memory T and plasma cells, are void of activation, proliferation and mobility.