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Effect of neuron‐derived neurotrophic factor on rejuvenation of human adipose‐derived stem cells for cardiac repair after myocardial infarction

机译:神经源性神经营养因子对人脂肪源性干细胞恢复活力在心肌梗死后的修复作用

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摘要

The decline of cell function caused by ageing directly impacts the therapeutic effects of autologous stem cell transplantation for heart repair. The aim of this study was to investigate whether overexpression of neuron‐derived neurotrophic factor (NDNF) can rejuvenate the adipose‐derived stem cells in the elderly and such rejuvenated stem cells can be used for cardiac repair. Human adipose‐derived stem cells (hADSCs) were obtained from donors age ranged from 17 to 92 years old. The effects of age on the biological characteristics of hADSCs and the expression of ageing‐related genes were investigated. The effects of transplantation of NDNF over‐expression stem cells on heart repair after myocardial infarction (MI) in adult mice were investigated. The proliferation, migration, adipogenic and osteogenic differentiation of hADSCs inversely correlated with age. The mRNA and protein levels of NDNF were significantly decreased in old (>60 years old) compared to young hADSCs (<40 years old). Overexpression of NDNF in old hADSCs significantly improved their proliferation and migration capacity in vitro. Transplantation of NDNF‐overexpressing old hADSCs preserved cardiac function through promoting angiogenesis on MI mice. NDNF rejuvenated the cellular function of aged hADSCs. Implantation of NDNF‐rejuvenated hADSCs improved angiogenesis and cardiac function in infarcted mouse hearts.
机译:由衰老引起的细胞功能下降直接影响自体干细胞移植对心脏修复的治疗效果。这项研究的目的是研究神经元衍生的神经营养因子(NDNF)的过度表达是否可以使老年人的脂肪干细胞恢复活力,并且这种恢复活力的干细胞可以用于心脏修复。人类脂肪干细胞(hADSCs)来自年龄在17至92岁之间的供体。研究了年龄对hADSCs生物学特性和衰老相关基因表达的影响。研究了成年小鼠心肌梗塞后NDNF高表达干细胞移植对心脏修复的影响。 hADSCs的增殖,迁移,成脂和成骨分化与年龄成反比。与年轻的hADSCs(<40岁)相比,老年人(> 60岁)NDNF的mRNA和蛋白水平显着降低。 NDNF在老hADSCs中的过量表达可显着改善其在体外的增殖和迁移能力。过度表达NDNF的旧hADSCs的移植通过促进MI小鼠的血管生成来保留心脏功能。 NDNF使衰老的hADSCs的细胞功能恢复活力。植入NDNF再生的hADSCs可改善梗死小鼠心脏的血管生成和心脏功能。

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