A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Transinteractome analysis reveals distinct niche requirements for isotype-based plasma cell subsets in the bone marrow
Tekijät: Bonaud Amélie, Larraufie Pierre, Khamyath Mélanie, Szachnowski Ugo, Flint Shaun M., Brunel-Meunier Nadège, Delhommeau François, Munier Annie, Lönnberg Tapio, Toffano-Nioche Claire, Gautheret Daniel, Balabanian Karl, Espéli Marion
Kustantaja: WILEY
Julkaisuvuosi: 2023
Journal: European Journal of Immunology
Tietokannassa oleva lehden nimi: EUROPEAN JOURNAL OF IMMUNOLOGY
Lehden akronyymi: EUR J IMMUNOL
Vuosikerta: 53
Numero: 9
Sivujen määrä: 9
ISSN: 0014-2980
eISSN: 1521-4141
DOI: https://doi.org/10.1002/eji.202250334
Verkko-osoite: https://onlinelibrary.wiley.com/doi/10.1002/eji.202250334
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/181211475
Bone marrow (BM) long-lived plasma cells (PCs) are essential for long-term protection against infection, and their persistence within this organ relies on interactions with Cxcl12-expressing stromal cells that are still not clearly identified. Here, using single cell RNAseq and in silico transinteractome analyses, we identified Leptin receptor positive (LepR+) mesenchymal cells as the stromal cell subset most likely to interact with PCs within the BM. Moreover, we demonstrated that depending on the isotype they express, PCs may use different sets of integrins and adhesion molecules to interact with these stromal cells. Altogether, our results constitute an unprecedented characterization of PC subset stromal niches and open new avenues for the specific targeting of BM PCs based on their isotype.
Ladattava julkaisu This is an electronic reprint of the original article. |