| Literature DB >> 35210623 |
Sethuraman Subramanian1,2,3, Clara Jana-Lui Busch1, Kaaweh Molawi2,3, Laufey Geirsdottir2, Julien Maurizio4, Stephanie Vargas Aguilar1,2,3, Hassiba Belahbib2, Gregory Gimenez2, Ridzky Anis Advent Yuda1, Michaela Burkon1, Jérémy Favret1, Sara Gholamhosseinian Najjar1, Bérengère de Laval2, Prashanth Kumar Kandalla1, Sandrine Sarrazin1,2, Lena Alexopoulou2, Michael H Sieweke5,6.
Abstract
Alveolar macrophages (AMs) are lung tissue-resident macrophages that can be expanded in culture, but it is unknown to what extent culture affects their in vivo identity. Here we show that mouse long-term ex vivo expanded AMs (exAMs) maintained a core AM gene expression program, but showed culture adaptations related to adhesion, metabolism and proliferation. Upon transplantation into the lung, exAMs reacquired full transcriptional and epigenetic AM identity, even after several months in culture and could self-maintain long-term in the alveolar niche. Changes in open chromatin regions observed in culture were fully reversible in transplanted exAMs and resulted in a gene expression profile indistinguishable from resident AMs. Our results indicate that long-term proliferation of AMs in culture did not compromise cellular identity in vivo. The robustness of exAM identity provides new opportunities for mechanistic analysis and highlights the therapeutic potential of exAMs.Entities:
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Year: 2022 PMID: 35210623 DOI: 10.1038/s41590-022-01146-w
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 31.250