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心脏成纤维细胞亚型反映病理性心脏重塑。

Cardiac fibroblast sub-types reflect pathological cardiac remodeling .

作者信息

Herum Kate Møller, Weng Guangzheng, Kahnert Konstantin, Waikel Rebekah, Milburn Greg, Conger Autumn, Anaya Paul, Campbell Kenneth S, Lundby Alicia, Won Kyoung Jae, Brakebusch Cord

机构信息

Biotech Research and Innovation Centre (BRIC), University of Copenhagen, 2200 Copenhagen, Denmark.

Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

出版信息

Matrix Biol Plus. 2022 Jun 6;15:100113. doi: 10.1016/j.mbplus.2022.100113. eCollection 2022 Aug.

Abstract

Many heart diseases are associated with fibrosis, but it is unclear whether different types of heart disease correlate with different subtypes of activated fibroblasts and to which extent such diversity is modeled during activation of primary cardiac fibroblasts. Analyzing the expression of 82 fibrosis related genes in 65 heart failure (HF) patients, we identified a panel of 12 genes clearly distinguishing HF patients better from healthy controls than measurement of the collagen-related hydroxyproline content. A subcluster enriched in ischemic HF was recognized, but not for diabetes, high BMI, or gender. Single-cell transcriptomic analysis of activated mouse cardiac fibroblasts distinguished 6 subpopulations, including a contractile Acta2 precursor population, which was predicted by time trajectory analysis to develop into Acta2 subpopulations with high production of extracellular matrix molecules. The 12 gene profile identified in HF patients showed highest similarity to the fibroblast subset with the strongest expression of extracellular matrix molecules. Population markers identified were furthermore able to clearly cluster different disease stages in a murine model for myocardial infarct. These data suggest that major features of cardiac fibroblast activation in heart failure patients, in murine heart disease models and in cell culture of primary murine cardiac fibroblast are shared.

摘要

许多心脏病都与纤维化相关,但目前尚不清楚不同类型的心脏病是否与活化成纤维细胞的不同亚型相关,以及在原代心脏成纤维细胞活化过程中这种多样性在多大程度上得以体现。通过分析65例心力衰竭(HF)患者中82个纤维化相关基因的表达,我们鉴定出一组12个基因,与测量胶原相关羟脯氨酸含量相比,这组基因能更有效地将HF患者与健康对照区分开来。我们识别出一个富含缺血性HF的亚群,但糖尿病、高体重指数或性别不存在这种情况。对活化的小鼠心脏成纤维细胞进行单细胞转录组分析,区分出6个亚群,包括一个收缩性肌动蛋白α2(Acta2)前体细胞群,通过时间轨迹分析预测该细胞群会发展成高分泌细胞外基质分子的Acta2亚群。在HF患者中鉴定出的12个基因谱与细胞外基质分子表达最强的成纤维细胞亚群最为相似。此外,所鉴定的群体标志物能够在心肌梗死小鼠模型中清晰地划分不同疾病阶段。这些数据表明,心力衰竭患者、小鼠心脏病模型以及原代小鼠心脏成纤维细胞的细胞培养中,心脏成纤维细胞活化的主要特征是相同的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c27/9198323/b22a5584778a/gr1.jpg

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