缺血性心肌病
心力衰竭
转录组
心室
生物
心肌病
扩张型心肌病
内科学
心脏病学
生物信息学
细胞生物学
医学
基因
基因表达
射血分数
遗传学
作者
Bridget Simonson,Mark Chaffin,Matthew C. Hill,Ondine Atwa,Yasmine Guedira,Harshit Bhasin,Amelia Weber Hall,Sikander Hayat,Simon J. Baumgart,Kenneth Bedi,Kenneth B. Margulies,Carla Klattenhoff,Patrick T. Ellinor
出处
期刊:Cell Reports
[Elsevier]
日期:2023-02-01
卷期号:42 (2): 112086-112086
被引量:21
标识
DOI:10.1016/j.celrep.2023.112086
摘要
Ischemic cardiomyopathy (ICM) is the leading cause of heart failure worldwide, yet the cellular and molecular signature of this disease is largely unclear. Using single-nucleus RNA sequencing (snRNA-seq) and integrated computational analyses, we profile the transcriptomes of over 99,000 human cardiac nuclei from the non-infarct region of the left ventricle of 7 ICM transplant recipients and 8 non-failing (NF) controls. We find the cellular composition of the ischemic heart is significantly altered, with decreased cardiomyocytes and increased proportions of lymphatic, angiogenic, and arterial endothelial cells in patients with ICM. We show that there is increased LAMININ signaling from endothelial cells to other cell types in ICM compared with NF. Finally, we find that the transcriptional changes that occur in ICM are similar to those in hypertrophic and dilated cardiomyopathies and that the mining of these combined datasets can identify druggable genes that could be used to target end-stage heart failure.
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