| Literature DB >> 35065706 |
Dachuan Zhang1, Xin Gao2, Huihui Li2, Daniel K Borger2, Qiaozhi Wei2, Eva Yang2, Chunliang Xu2, Sandra Pinho2, Paul S Frenette3.
Abstract
Host microbiota crosstalk is essential for the production and functional modulation of blood-cell lineages. Whether, and if so how, the microbiota influences hematopoietic stem cells (HSCs) is unclear. Here, we show that the microbiota regulates HSC self-renewal and differentiation under stress conditions by modulating local iron availability in the bone marrow (BM). In microbiota-depleted mice, HSC self-renewal was enhanced during regeneration, while the commitment toward differentiation was dramatically compromised. Mechanistically, microbiota depletion selectively impaired the recycling of red blood cells (RBCs) by BM macrophages, resulting in reduced local iron levels without affecting systemic iron homeostasis. Limiting iron availability in food (in vivo) or in culture (ex vivo), or by CD169+ macrophage depletion, enhanced HSC self-renewal and expansion. These results reveal an intricate interplay between the microbiota, macrophages, and iron, and their essential roles in regulating critical HSC fate decisions under stress.Entities:
Keywords: erythrophagocytosis; fate decision; hematopoietic regeneration; hematopoietic stem cell; iron; macrophage; microbiota; self-renewal
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Year: 2022 PMID: 35065706 PMCID: PMC8818037 DOI: 10.1016/j.stem.2021.12.009
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633