Bone marrow neutrophil density regulates myelopoiesis during obesity and weight loss.

IF 12.6 1区 医学 Q1 IMMUNOLOGY
Journal of Experimental Medicine Pub Date : 2025-09-01 Epub Date: 2025-07-11 DOI:10.1084/jem.20242174
Quin T Waterbury, Jin Qian, Hualong Zheng, Amanda Dirnberger, Oakley C Olson, Ruth A White, Feijing Wu, Hiroki Kobayashi, Ermanno Malagola, Yosuke Ochiai, Ruhong Tu, Biyun Zheng, Adama Diaby, Harry Nagendra, Jonathan S LaBella, Leah Zamechek, Judith Korner, Ana B Emiliano, Anthony W Ferrante, Emmanuelle Passegué, Timothy C Wang
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引用次数: 0

Abstract

The bone marrow (BM) is altered in obesity to promote myeloid cell generation, but the mechanisms driving these changes remain unclear. Here, we show that obesogenic stimuli promote adipose tissue macrophages to recruit neutrophils from the BM in mice. Recruitment of BM neutrophils activates hematopoietic stem cells, which produce myeloid cells that accumulate in the circulation and drive inflammation. This recruitment is not resolved by weight loss, leading to sustained myelopoiesis in previously obese mice. Inhibiting neutrophil recruitment out of the BM in obese mice or during weight loss reduces BM myelopoiesis and adipose tissue inflammation, and improves glucose tolerance. In humans with obesity, plasma neutrophil chemokines are increased, correlate with increased insulin resistance, but do not decrease with weight loss. Our results demonstrate that neutrophil recruitment is a key mediator of myelopoiesis during obesity, and targeting this pathway is a potential strategy to improve inflammation during obesity and weight loss.

在肥胖和减肥期间,骨髓中性粒细胞密度调节骨髓生成。
肥胖会改变骨髓(BM)以促进骨髓细胞的生成,但驱动这些变化的机制尚不清楚。本研究表明,致肥性刺激可促进小鼠脂肪组织巨噬细胞从BM中募集中性粒细胞。BM中性粒细胞的募集激活造血干细胞,造血干细胞产生髓样细胞,髓样细胞在循环中积累并驱动炎症。这种招募不能通过体重减轻来解决,从而导致先前肥胖的小鼠持续的骨髓生成。抑制肥胖小鼠或减肥期间BM外的中性粒细胞募集可减少BM骨髓生成和脂肪组织炎症,并改善葡萄糖耐量。在肥胖人群中,血浆中性粒细胞趋化因子增加,与胰岛素抵抗增加相关,但不随体重减轻而减少。我们的研究结果表明,中性粒细胞募集是肥胖期间骨髓生成的关键介质,靶向这一途径是改善肥胖和减肥期间炎症的潜在策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
26.60
自引率
1.30%
发文量
189
审稿时长
3-8 weeks
期刊介绍: Since its establishment in 1896, the Journal of Experimental Medicine (JEM) has steadfastly pursued the publication of enduring and exceptional studies in medical biology. In an era where numerous publishing groups are introducing specialized journals, we recognize the importance of offering a distinguished platform for studies that seamlessly integrate various disciplines within the pathogenesis field. Our unique editorial system, driven by a commitment to exceptional author service, involves two collaborative groups of editors: professional editors with robust scientific backgrounds and full-time practicing scientists. Each paper undergoes evaluation by at least one editor from both groups before external review. Weekly editorial meetings facilitate comprehensive discussions on papers, incorporating external referee comments, and ensure swift decisions without unnecessary demands for extensive revisions. Encompassing human studies and diverse in vivo experimental models of human disease, our focus within medical biology spans genetics, inflammation, immunity, infectious disease, cancer, vascular biology, metabolic disorders, neuroscience, and stem cell biology. We eagerly welcome reports ranging from atomic-level analyses to clinical interventions that unveil new mechanistic insights.
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