Author
Listed:
- René Riedel
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association
Max Planck Institute for Evolutionary Biology)
- Richard Addo
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Marta Ferreira-Gomes
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Gitta Anne Heinz
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Frederik Heinrich
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Jannis Kummer
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Victor Greiff
(Eidgenössische Technische Hochschule (ETH Zürich)
University of Oslo)
- Daniel Schulz
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Cora Klaeden
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Rebecca Cornelis
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Ulrike Menzel
(Eidgenössische Technische Hochschule (ETH Zürich))
- Stefan Kröger
(Humboldt-Universität zu Berlin
Robert Koch Institute)
- Ulrik Stervbo
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association
Charité-Universitätsmedizin Berlin)
- Ralf Köhler
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Claudia Haftmann
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association
Universitätsspital Zürich)
- Silvia Kühnel
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Katrin Lehmann
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Patrick Maschmeyer
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Mairi McGrath
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Sandra Naundorf
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Stefanie Hahne
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Özen Sercan-Alp
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association
Industriepark Hoechst)
- Francesco Siracusa
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association
University Medical Center Hamburg-Eppendorf)
- Jonathan Stefanowski
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association
Charité-Universitätsmedizin Berlin)
- Melanie Weber
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Kerstin Westendorf
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Jakob Zimmermann
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association
University of Bern)
- Anja E. Hauser
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association
Charité-Universitätsmedizin Berlin)
- Sai T. Reddy
(Eidgenössische Technische Hochschule (ETH Zürich))
- Pawel Durek
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Hyun-Dong Chang
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
- Mir-Farzin Mashreghi
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association
BCRT/DRFZ Single-Cell Laboratory for Advanced Cellular Therapies - Brandenburg Center for Regenerative Therapies (BCRT))
- Andreas Radbruch
(Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association)
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.
Suggested Citation
René Riedel & Richard Addo & Marta Ferreira-Gomes & Gitta Anne Heinz & Frederik Heinrich & Jannis Kummer & Victor Greiff & Daniel Schulz & Cora Klaeden & Rebecca Cornelis & Ulrike Menzel & Stefan Krög, 2020.
"Discrete populations of isotype-switched memory B lymphocytes are maintained in murine spleen and bone marrow,"
Nature Communications, Nature, vol. 11(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-16464-6
DOI: 10.1038/s41467-020-16464-6
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