B lymphocyte-derived acetylcholine limits steady-state and emergency hematopoiesis

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作者
Maximilian J. Schloss
Maarten Hulsmans
David Rohde
I-Hsiu Lee
Nicolas Severe
Brody H. Foy
Fadi E. Pulous
Shuang Zhang
Konstantinos D. Kokkaliaris
Vanessa Frodermann
Gabriel Courties
Chongbo Yang
Yoshiko Iwamoto
Anders Steen Knudsen
Cameron S. McAlpine
Masahiro Yamazoe
Stephen P. Schmidt
Gregory R. Wojtkiewicz
Gustavo Santos Masson
Karin Gustafsson
Diane Capen
Dennis Brown
John M. Higgins
David T. Scadden
Peter Libby
Filip K. Swirski
Kamila Naxerova
Matthias Nahrendorf
机构
[1] Massachusetts General Hospital Research Institute and Harvard Medical School,Center for Systems Biology
[2] Massachusetts General Hospital,Department of Radiology
[3] Harvard University,Department of Stem Cell and Regenerative Biology
[4] Massachusetts General Hospital,Center for Regenerative Medicine and Cancer Center
[5] Cardiovascular Research Institute,Program in Membrane Biology, Division of Nephrology, Department of Medicine
[6] Icahn School of Medicine at Mount Sinai,Division of Cardiovascular Medicine, Department of Medicine
[7] Harvard Stem Cell Institute,Cardiovascular Research Center
[8] Harvard Medical School and Massachusetts General Hospital,Department of Internal Medicine I
[9] Brigham and Women’s Hospital and Harvard Medical School,undefined
[10] Massachusetts General Hospital and Harvard Medical School,undefined
[11] University Hospital Wuerzburg,undefined
来源
Nature Immunology | 2022年 / 23卷
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摘要
Autonomic nerves control organ function through the sympathetic and parasympathetic branches, which have opposite effects. In the bone marrow, sympathetic (adrenergic) nerves promote hematopoiesis; however, how parasympathetic (cholinergic) signals modulate hematopoiesis is unclear. Here, we show that B lymphocytes are an important source of acetylcholine, a neurotransmitter of the parasympathetic nervous system, which reduced hematopoiesis. Single-cell RNA sequencing identified nine clusters of cells that expressed the cholinergic α7 nicotinic receptor (Chrna7) in the bone marrow stem cell niche, including endothelial and mesenchymal stromal cells (MSCs). Deletion of B cell-derived acetylcholine resulted in the differential expression of various genes, including Cxcl12 in leptin receptor+ (LepR+) stromal cells. Pharmacologic inhibition of acetylcholine esterase decreased the systemic supply of inflammatory myeloid cells in mice and humans with cardiovascular disease.
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页码:605 / 618
页数:13
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