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基于人脂肪间充质干细胞的微球体外改善动脉粥样硬化进展。

Human Adipose-Derived Mesenchymal Stem Cell-Based Microspheres Ameliorate Atherosclerosis Progression In Vitro.

机构信息

Regenerative Medicine Research Center, Sichuan University West China Hospital, Chengdu, China.

Department of Clinical Laboratory, the Sixth People's Hospital of Chengdu, Chengdu, China.

出版信息

Stem Cells Dev. 2023 Jun;32(11-12):314-330. doi: 10.1089/scd.2022.0287. Epub 2023 Apr 3.

Abstract

Atherosclerosis (AS) is a chronic inflammatory disease associated with lipid deposition, which could be converted into acute clinical events by thrombosis or plaque rupture. Adipose-derived mesenchymal stem cell (ADSC)-encapsulated repair units could be an effective cure for the treatment of AS patients. In this study, we encapsulate human adipose-derived mesenchymal stem cells (hADSCs) in collagen microspheres to fabricate stem cell repair units. Besides, we show that encapsulation in collagen microspheres and cultured in vitro for 14 days maintain the viability and stemness of hADSCs. Moreover, we generate AS progression model and niche in vitro by combining hyperlipemia serum of AS patients with AS cell models. We further systematically demonstrate that hADSC-based microspheres could ameliorate AS progression by inhibiting oxidative stress injury, cell apoptosis, endothelial dysfunction, inflammation, and lipid accumulation. In addition, we perform transcriptomic analysis and functional studies to demonstrate how hADSCs (three dimensional cultured in microspheres) respond to AS niche compared with healthy microenvironment. These findings reveal a role for ADSC-based microspheres in the treatment of AS and provide new ideas for stem cell therapy in cardiovascular disease. The results may have implications for improving the efficiency of hADSC therapies by illuminating the mechanisms of hADSCs exposed in special pathological niche.

摘要

动脉粥样硬化(AS)是一种与脂质沉积相关的慢性炎症性疾病,可通过血栓形成或斑块破裂转化为急性临床事件。脂肪来源的间充质干细胞(ADSC)包封修复单元可能是治疗 AS 患者的有效方法。在这项研究中,我们将人脂肪来源的间充质干细胞(hADSCs)包封在胶原微球中,以制备干细胞修复单元。此外,我们还表明,在胶原微球中包封并在体外培养 14 天可以维持 hADSCs 的活力和干性。此外,我们通过将 AS 患者的高脂血症血清与 AS 细胞模型结合,在体外生成 AS 进展模型和龛位。我们进一步系统地证明,基于 hADSC 的微球可以通过抑制氧化应激损伤、细胞凋亡、内皮功能障碍、炎症和脂质积累来改善 AS 进展。此外,我们进行了转录组分析和功能研究,以证明 hADSCs(在微球中三维培养)如何与健康微环境相比对 AS 龛位做出反应。这些发现揭示了基于 ADSC 的微球在治疗 AS 中的作用,并为心血管疾病中的干细胞治疗提供了新的思路。这些结果可能通过阐明在特殊病理龛位中暴露的 hADSCs 的机制,提高 hADSC 治疗的效率。

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