Back to Search Start Over

Microbiota-derived lactate promotes hematopoiesis and erythropoiesis by inducing stem cell factor production from leptin receptor+ niche cells.

Authors :
Lee YS
Kim TY
Kim Y
Kim S
Lee SH
Seo SU
Zhou BO
Eunju O
Kim KS
Kweon MN
Source :
Experimental & molecular medicine [Exp Mol Med] 2021 Sep; Vol. 53 (9), pp. 1319-1331. Date of Electronic Publication: 2021 Sep 09.
Publication Year :
2021

Abstract

Although functional interplay between intestinal microbiota and distant sites beyond the gut has been identified, the influence of microbiota-derived metabolites on hematopoietic stem cells (HSCs) remains unclear. This study investigated the role of microbiota-derived lactate in hematopoiesis using mice deficient in G-protein-coupled receptor (Gpr) 81 (Gpr81 <superscript>-</superscript> <superscript>/-</superscript> ), an established lactate receptor. We detected significant depletion of total HSCs in the bone marrow (BM) of Gpr81 <superscript>-/-</superscript> mice compared with heterogenic (Gpr81 <superscript>+/-</superscript> ) mice in a steady state. Notably, the expression levels of stem cell factor (SCF), which is required for the proliferation of HSCs, decreased significantly in leptin receptor-expressing (LepR <superscript>+</superscript> ) mesenchymal stromal cells (MSCs) around the sinusoidal vessels of the BM from Gpr81 <superscript>-/-</superscript> mice compared with Gpr81 <superscript>+/-</superscript> mice. Hematopoietic recovery and activation of BM niche cells after irradiation or busulfan treatment also required Gpr81 signals. Oral administration of lactic acid-producing bacteria (LAB) activated SCF secretion from LepR <superscript>+</superscript> BM MSCs and subsequently accelerated hematopoiesis and erythropoiesis. Most importantly, LAB feeding accelerated the self-renewal of HSCs in germ-free mice. These results suggest that microbiota-derived lactate stimulates SCF secretion by LepR <superscript>+</superscript> BM MSCs and subsequently activates hematopoiesis and erythropoiesis in a Gpr81-dependent manner.<br /> (© 2021. The Author(s).)

Details

Language :
English
ISSN :
2092-6413
Volume :
53
Issue :
9
Database :
MEDLINE
Journal :
Experimental & molecular medicine
Publication Type :
Academic Journal
Accession number :
34497346
Full Text :
https://doi.org/10.1038/s12276-021-00667-y