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

IF 2.5 3区 医学 Q3 CELL & TISSUE ENGINEERING Stem cells and development Pub Date : 2023-06-01 DOI:10.1089/scd.2022.0287
Shaojie Yang, Xiong Xiao, Ziwei Huang, Qingyun Chen, Chenxi Li, Chuan Niu, Yuchu Yang, Liping Yang, Li Feng
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引用次数: 1

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.

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人脂肪来源的间充质干细胞微球在体外改善动脉粥样硬化进展。
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。脂肪源性间充质干细胞(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)封装在胶原微球中,以制造干细胞修复单元。此外,我们发现胶原微球包封和体外培养14天可以保持hascs的活力和干性。此外,我们将AS患者高脂血症血清与AS细胞模型相结合,在体外建立AS进展模型和生态位。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的进展。此外,我们进行转录组学分析和功能研究,以证明与健康微环境相比,hscs(在微球中三维培养)对AS生态位的反应。这些发现揭示了基于adsc的微球在AS治疗中的作用,并为心血管疾病的干细胞治疗提供了新的思路。这些结果可能通过阐明hADSC暴露于特殊病理生态位的机制,对提高hADSC治疗的效率具有启示意义。
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来源期刊
Stem cells and development
Stem cells and development 医学-细胞与组织工程
CiteScore
7.80
自引率
2.50%
发文量
69
审稿时长
3 months
期刊介绍: Stem Cells and Development is globally recognized as the trusted source for critical, even controversial coverage of emerging hypotheses and novel findings. With a focus on stem cells of all tissue types and their potential therapeutic applications, the Journal provides clinical, basic, and translational scientists with cutting-edge research and findings. Stem Cells and Development coverage includes: Embryogenesis and adult counterparts of this process Physical processes linking stem cells, primary cell function, and structural development Hypotheses exploring the relationship between genotype and phenotype Development of vasculature, CNS, and other germ layer development and defects Pluripotentiality of embryonic and somatic stem cells The role of genetic and epigenetic factors in development
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