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神经元衍生神经营养因子对心肌梗死后人心源性脂肪干细胞心脏修复再生的影响。

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

机构信息

Department of Biochemistry and Molecular Biology, Shanxi Key Laboratory of Birth Defect and Cell Regeneration, Shanxi Medical University, Taiyuan, China.

Department of Endocrinology, Shanxi Dayi Hospital affiliated to Shanxi Medical University, Taiyuan, China.

出版信息

J Cell Mol Med. 2019 Sep;23(9):5981-5993. doi: 10.1111/jcmm.14456. Epub 2019 Jul 9.

DOI:10.1111/jcmm.14456
PMID:31287219
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6714174/
Abstract

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.

摘要

衰老导致的细胞功能衰退会直接影响自体干细胞移植治疗心脏病的效果。本研究旨在探讨过表达神经营养因子(NDNF)能否使老年脂肪来源干细胞(ADSCs)年轻化,以及这种年轻化的干细胞能否用于心脏修复。从年龄在 17 岁至 92 岁的供者中获取人 ADSC。研究了年龄对 hADSC 生物学特性和衰老相关基因表达的影响。研究了过表达 NDNF 的干细胞移植对成年小鼠心肌梗死(MI)后心脏修复的影响。hADSC 的增殖、迁移、成脂和成骨分化与年龄呈负相关。与年轻 hADSC(<40 岁)相比,老年(>60 岁)hADSC 中的 NDNF mRNA 和蛋白水平显著降低。过表达 NDNF 可显著提高老年 hADSC 的体外增殖和迁移能力。在 MI 小鼠中,过表达 NDNF 的老年 hADSC 移植可通过促进血管生成来保护心脏功能。NDNF 使老年 hADSC 的细胞功能年轻化。植入 NDNF 年轻化的 hADSC 可改善梗死小鼠心脏的血管生成和心脏功能。

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本文引用的文献

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