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Vcam1+成纤维细胞脂肪生成祖细胞标记慢性肢体威胁性缺血中的脂肪浸润。

Vcam1+ Fibro-adipogenic Progenitors Mark Fatty Infiltration in Chronic Limb Threatening Ischemia.

作者信息

Dai Qunsheng, Wan Changxin, Xu Yueyuan, Fei Kaileen, Olivere Lindsey A, Garrett Brianna, Akers Leo, Peters Derek, Otto James, Kontos Christopher D, Ji Zhiceng, Diao Yarui, Southerland Kevin W

机构信息

Division of Vascular and Endovascular Surgery, Department of Surgery, Duke University Medical Center, Durham, NC, USA.

Department of Biostatistics and Bioinformatics, Duke University, Durham, NC, USA.

出版信息

bioRxiv. 2024 Jul 11:2024.07.08.602430. doi: 10.1101/2024.07.08.602430.

Abstract

Skeletal muscle health and function is a critical determinant of clinical outcomes in patients with peripheral arterial disease (PAD). Herein, we identify fatty infiltration, the ectopic deposition of adipocytes in skeletal muscle, as a histological hallmark of end-stage PAD, also known as chronic limb threatening ischemia (CLTI). Leveraging single cell transcriptome mapping in mouse models of PAD, we identify a pro-adipogenic mesenchymal stromal cell population marked by expression of Vcam1 (termed Vcam1+ FAPs) that expands in the ischemic limb. Mechanistically, we identify Sfrp1 and Nr3c1 as regulators of Vcam1+ FAP adipogenic differentiation. Loss of Sfrp1 and Nr3c1 impair Vcam1+ FAP differentiation into adipocytes . Finally, we show that Vcam1+ FAPs are enriched in human CLTI patients. Collectively, our results identify a pro-adipogenic FAP subpopulation in CLTI patients and provide a potential therapeutic target for muscle regeneration in PAD.

摘要

骨骼肌健康与功能是外周动脉疾病(PAD)患者临床预后的关键决定因素。在此,我们确定脂肪浸润,即脂肪细胞在骨骼肌中的异位沉积,是终末期PAD(也称为慢性肢体威胁性缺血,CLTI)的组织学标志。利用PAD小鼠模型中的单细胞转录组图谱,我们鉴定出一个以Vcam1表达为特征的促脂肪生成间充质基质细胞群体(称为Vcam1+ FAPs),该群体在缺血肢体中扩增。从机制上讲,我们确定Sfrp1和Nr3c1是Vcam1+ FAP脂肪生成分化的调节因子。Sfrp1和Nr3c1的缺失会损害Vcam1+ FAP向脂肪细胞的分化。最后,我们表明Vcam1+ FAPs在人类CLTI患者中富集。总体而言,我们的结果确定了CLTI患者中一个促脂肪生成的FAP亚群,并为PAD中的肌肉再生提供了一个潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2b3/11257459/785ecd59193d/nihpp-2024.07.08.602430v1-f0001.jpg

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