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生成一种新型模型以研究再内皮化。

Generation of a novel model to study re-endothelialization.

机构信息

Centre for Tissue Engineering and Regenerative Medicine, Faculty of Medicine, Universiti Kebangsaan Malaysia, Cheras, Malaysia.

Faculty of Applied Sciences, Universiti Teknologi MARA, Perak Branch, Tapah Campus, Perak, Malaysia.

出版信息

Artif Cells Nanomed Biotechnol. 2023 Dec;51(1):408-416. doi: 10.1080/21691401.2023.2245456.

Abstract

Endothelial dysfunction initiates the pathogenesis of a myriad of cardiovascular diseases, yet the precise underlying mechanisms remain unclear. Current model utilises mechanical denudation of arteries resulting in an arterial-injury model with onset of intimal hyperplasia (IH). Our study shows that 5 min enzymatic denudation of human umbilical artery (hUA) lumen at 37 °C efficiently denudes hUA while maintaining vessel integrity without significantly increase intima-media thickness after 7 days in culture. This ex-vivo model will be a valuable tool in understanding the mechanism of re-endothelialization prior to smooth muscle cells (SMC) activation thus placating IH at an early stage.

摘要

内皮功能障碍引发了无数心血管疾病的发病机制,但确切的潜在机制仍不清楚。目前的模型利用动脉的机械剥脱,导致动脉损伤模型,从而引发内膜增生(IH)。我们的研究表明,在 37°C 下对人脐动脉(hUA)管腔进行 5 分钟的酶学剥脱,可有效地剥脱 hUA,同时保持血管完整性,在培养 7 天后,内膜-中膜厚度无明显增加。这种离体模型将是理解平滑肌细胞(SMC)激活前再内皮化机制的有用工具,从而在早期抑制 IH。

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