| Literature DB >> 30893599 |
Marielle Balzano1, Maria De Grandis2, Thien-Phong Vu Manh3, Lionel Chasson3, Florence Bardin2, Anne Farina4, Arnauld Sergé2, Ghislain Bidaut2, Pierre Charbord5, Léonard Hérault6, Anne-Laure Bailly2, Amandine Cartier-Michaud2, Annie Boned3, Marc Dalod3, Estelle Duprez2, Paul Genever7, Mark Coles8, Marc Bajenoff3, Luc Xerri9, Michel Aurrand-Lions10, Claudine Schiff3, Stéphane J C Mancini11.
Abstract
In the bone marrow, CXCL12 and IL-7 are essential for B cell differentiation, whereas hematopoietic stem cell (HSC) maintenance requires SCF and CXCL12. Peri-sinusoidal stromal (PSS) cells are the main source of IL-7, but their characterization as a pro-B cell niche remains limited. Here, we characterize pro-B cell supporting stromal cells and decipher the interaction network allowing pro-B cell retention. Preferential contacts are found between pro-B cells and PSS cells, which homogeneously express HSC and B cell niche genes. Furthermore, pro-B cells are frequently located in the vicinity of HSCs in the same niche. Using an interactome bioinformatics pipeline, we identify Nidogen-1 as essential for pro-B cell retention in the peri-sinusoidal niche as confirmed in Nidogen-1-/- mice. Finally, human pro-B cells and hematopoietic progenitors are observed close to similar IL-7+ stromal cells. Thus, a multispecific niche exists in mouse and human supporting both early progenitors and committed hematopoietic lineages.Entities:
Keywords: B cell development; bone marrow; hematopoietic stem cell; interaction network; stromal cell niche
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Year: 2019 PMID: 30893599 DOI: 10.1016/j.celrep.2019.02.065
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423