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恒河猴骨髓间充质干细胞的年龄相关性变化。

Age-related changes in mesenchymal stem cells derived from rhesus macaque bone marrow.

机构信息

Division of Gene Therapy, Tulane National Primate Research Center, Covington, LA 70433, USA.

出版信息

Aging Cell. 2011 Feb;10(1):66-79. doi: 10.1111/j.1474-9726.2010.00646.x.

Abstract

The regeneration potential of mesenchymal stem cells (MSCs) diminishes with advanced age and this diminished potential is associated with changes in cellular functions. This study compared MSCs isolated from the bone marrow of rhesus monkeys (rBMSCs) in three age groups: young (< 5 years), middle (8-10 years), and old (> 12 years). The effects of aging on stem cell properties and indicators of stem cell fitness such as proliferation, differentiation, circadian rhythms, stress response proteins, miRNA expression, and global histone modifications in rBMSCs were analyzed. rBMSCs demonstrated decreased capacities for proliferation and differentiation as a function of age. The production of heat shock protein 70 (HSP70) and heat shock factor 1 (HSF1) were also reduced with increasing age. The level of a core circadian protein, Rev-erb α, was significantly increased in rBMSCs from old animals. Furthermore, analysis of miRNA expression profiles revealed an up-regulation of mir-766 and mir-558 and a down-regulation of mir-let-7f, mir-125b, mir-222, mir-199-3p, mir-23a, and mir-221 in old rBMSCs compare to young rBMSCs. However, there were no significant age-related changes in the global histone modification profiles of the four histone core proteins: H2A, H2B, H3, and H4 on rBMSCs. These changes represent novel insights into the aging process and could have implications regarding the potential for autologous stem cells therapy in older patients.

摘要

间充质干细胞(MSCs)的再生潜力随着年龄的增长而降低,这种降低的潜力与细胞功能的变化有关。本研究比较了来自三个年龄段恒河猴(rBMSCs)骨髓的 MSC:年轻(<5 岁)、中年(8-10 岁)和老年(>12 岁)。分析了衰老对干细胞特性和干细胞适应性指标的影响,如增殖、分化、昼夜节律、应激反应蛋白、miRNA 表达和 rBMSCs 中的全局组蛋白修饰。rBMSCs 的增殖和分化能力随着年龄的增长而降低。热休克蛋白 70(HSP70)和热休克因子 1(HSF1)的产生也随着年龄的增长而减少。衰老动物的 rBMSCs 中核心昼夜节律蛋白 Rev-erbα 的水平显著增加。此外,miRNA 表达谱分析显示,衰老 rBMSCs 中 mir-766 和 mir-558 的表达上调,mir-let-7f、mir-125b、mir-222、mir-199-3p、mir-23a 和 mir-221 的表达下调。然而,在四个核心组蛋白(H2A、H2B、H3 和 H4)的 rBMSCs 中,没有发现与年龄相关的组蛋白整体修饰谱的显著变化。这些变化代表了对衰老过程的新见解,可能对老年患者自体干细胞治疗的潜力具有重要意义。

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