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

被引:135
作者
Yu, Ji Min [1 ,2 ]
Wu, Xiying [3 ]
Gimble, Jeffrey M. [3 ]
Guan, Xiaoyan [4 ]
Freitas, Michael A. [4 ]
Bunnell, Bruce A. [1 ,2 ,5 ]
机构
[1] Tulane Natl Primate Res Ctr, Div Gene Therapy, Covington, LA 70433 USA
[2] Tulane Univ, Sch Med, Ctr Stem Cell Res & Regenerat Med, New Orleans, LA 70112 USA
[3] Pennington Biomed Res Ctr, Stem Cell Biol Lab, Baton Rouge, LA 70808 USA
[4] Ohio State Univ, Coll Med, Columbus, OH 43210 USA
[5] Tulane Univ, Sch Med, Dept Pharmacol, New Orleans, LA 70112 USA
基金
美国国家卫生研究院;
关键词
aging; cell cycle; differentiation; mesenchymal stem cells; miRNA; non-human primate; HISTONE POSTTRANSLATIONAL MODIFICATIONS; REV-ERBA-ALPHA; STROMAL CELLS; CIRCADIAN SYSTEM; DNA-DAMAGE; GENE PER1; LIQUID-CHROMATOGRAPHY; TRANSCRIPTION FACTORS; PROTEIN EXPRESSION; PROGENITOR CELLS;
D O I
10.1111/j.1474-9726.2010.00646.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
P>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 alpha, 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.
引用
收藏
页码:66 / 79
页数:14
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