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细胞间通讯和细胞外基质信号转导改变作为人类肥厚型心肌病的潜在疾病机制。

Altered intercellular communication and extracellular matrix signaling as a potential disease mechanism in human hypertrophic cardiomyopathy.

机构信息

Molecular Cardiology Research Institute, Tufts Medical Center, 800 Washington Street, Box 80, Boston, MA, 02111, USA.

CardioVascular Center, Tufts Medical Center, Boston, MA, USA.

出版信息

Sci Rep. 2022 Mar 25;12(1):5211. doi: 10.1038/s41598-022-08561-x.

Abstract

Hypertrophic cardiomyopathy (HCM) is considered a primary disorder of the sarcomere resulting in unexplained left ventricular hypertrophy but the paradoxical association of nonmyocyte phenotypes such as fibrosis, mitral valve anomalies and microvascular occlusion is unexplained. To understand the interplay between cardiomyocyte and nonmyocyte cell types in human HCM, single nuclei RNA-sequencing was performed on myectomy specimens from HCM patients with left ventricular outflow tract obstruction and control samples from donor hearts free of cardiovascular disease. Clustering analysis based on gene expression patterns identified a total of 34 distinct cell populations, which were classified into 10 different cell types based on marker gene expression. Differential gene expression analysis comparing HCM to Normal datasets revealed differences in sarcomere and extracellular matrix gene expression. Analysis of expressed ligand-receptor pairs across multiple cell types indicated profound alteration in HCM intercellular communication, particularly between cardiomyocytes and fibroblasts, fibroblasts and lymphocytes and involving integrin β1 and its multiple extracellular matrix (ECM) cognate ligands. These findings provide a paradigm for how sarcomere dysfunction is associated with reduced cardiomyocyte secretion of ECM ligands, altered fibroblast ligand-receptor interactions with other cell types and increased fibroblast to lymphocyte signaling, which can further alter the ECM composition and promote nonmyocyte phenotypes.

摘要

肥厚型心肌病(HCM)被认为是肌节的原发性疾病,导致无法解释的左心室肥厚,但纤维化、二尖瓣异常和微血管闭塞等非心肌细胞表型的反常关联仍无法解释。为了了解人类 HCM 中心肌细胞和非心肌细胞类型之间的相互作用,对伴有左心室流出道梗阻的 HCM 患者的心肌切除术标本和无心血管疾病的供体心脏对照标本进行了单细胞 RNA 测序。基于基因表达模式的聚类分析总共鉴定出 34 种不同的细胞群,根据标记基因表达将其分为 10 种不同的细胞类型。比较 HCM 与正常数据集的差异基因表达分析显示,肌节和细胞外基质基因表达存在差异。对多个细胞类型中表达的配体-受体对的分析表明,HCM 细胞间通讯发生了深刻变化,特别是在心肌细胞和成纤维细胞、成纤维细胞和淋巴细胞之间,涉及整合素β1及其多个细胞外基质(ECM)同源配体。这些发现为肌节功能障碍如何与心肌细胞 ECM 配体分泌减少、成纤维细胞与其他细胞类型的配体-受体相互作用改变以及成纤维细胞向淋巴细胞信号转导增加相关提供了范例,这些改变可以进一步改变 ECM 组成并促进非心肌细胞表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/728d/8956620/2db1b5234a36/41598_2022_8561_Fig1_HTML.jpg

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