Single‐Cell Transcriptomic Census of Endothelial Changes Induced by Matrix Stiffness and the Association with Atherosclerosis. (12th September 2022)

• Record Type: Journal Article
• Authors: Zamani, Maedeh; Cheng, Yu‐Hao; Charbonier, Frank; Gupta, Vivek Kumar; Mayer, Aaron T.; Trevino, Alexandro E.; Quertermous, Thomas; Chaudhuri, Ovijit; Cahan, Patrick; Huang, Ngan F.
• Is Part Of: Advanced functional materials. Volume 32:Number 47(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-09-12
• Subjects: atherosclerosis -- endothelial phenotypes -- endothelial‐to‐mesenchymal transition -- extracellular matrix stiffness -- single‐cell RNA sequencing; Materials -- Periodicals; Chemical vapor deposition -- Periodicals; 620.11
• DOI: 10.1002/adfm.202203069
• Languages: English
• ISSNs: 1616-301X

Abstract

Abstract: Vascular endothelial cell (EC) plasticity plays a critical role in the progression of atherosclerosis by giving rise to mesenchymal phenotypes in the plaque lesion. Despite the evidence for arterial stiffening as a major contributor to atherosclerosis, the complex interplay among atherogenic stimuli in vivo has hindered attempts to determine the effects of extracellular matrix (ECM) stiffness on endothelial‐mesenchymal transition (EndMT). To study the regulatory effects of ECM stiffness on EndMT, an in vitro model is developed in which human coronary artery ECs are cultured on physiological or pathological stiffness substrates. Leveraging single‐cell RNA sequencing, cell clusters with mesenchymal transcriptional features are identified to be more prevalent on pathological substrates than physiological substrates. Trajectory inference analyses reveal a novel mesenchymal‐to‐endothelial reverse transition, which is blocked by pathological stiffness substrates, in addition to the expected EndMT trajectory. ECs pushed to a mesenchymal character by pathological stiffness substrates are enriched in transcriptional signatures of atherosclerotic ECs from human and murine plaques. This study characterizes at single‐cell resolution the transcriptional programs that underpin EC plasticity in both physiological or pathological milieus, and thus serves as a valuable resource for more precisely defining EndMT and the transcriptional programs contributing to atherosclerosis. Abstract : Their findings suggest that endothelial cells (ECs, lining the inner surface of arteries) on stiff substrates turn into a heterogeneous cell population mainly consisted of the cells expressing non‐EC markers. In contrast, ECs are more protected from losing their healthy phenotype on substrates with physiological stiffness. This can explain the association between arterial stiffness and narrowing of the arteries, mediated through ECs phenotypic change.