AICAR, a small chemical molecule, primes osteogenic differentiation of adult mesenchymal stem cells

被引:31
|
作者
Wu, Wei [1 ]
Ye, Zhaoyang [1 ]
Zhou, Yan [1 ]
Tan, Wen-Song [1 ]
机构
[1] E China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
AICAR; Mesenchymal stem cells; Differentiation; Osteogenesis; Small molecule; ANTIDIABETIC DRUG METFORMIN; ACTIVATED PROTEIN-KINASE; APOPTOSIS; PATHWAY; MINERALIZATION; PROLIFERATION; STIMULATION; ADIPONECTIN; OSTEOBLASTS; INHIBITION;
D O I
10.5301/ijao.5000007
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The chemical approach to controlling stem cell fates is emerging as a powerful tool, holding great promise in tissue engineering and regenerative medicine. Various small molecules have been demonstrated capable of modulating stem cell differentiation. In this paper, we studied the effects of 5-aminoimidazole-4-carboxamide-1-beta-riboside (AICAR), an activator of AMP-activated protein kinase (AMPK), on mesenchymal stem cells (MSCs). AICAR at high concentrations (1.0-2.0 mM) significantly inhibited proliferation of both human amnion-derived MSCs (hAMSCs) and rabbit bone marrow-derived MSCs (BM-MSCs). Most importantly, AICAR efficiently promoted the osteogenic differentiation of hAMSCs and BM-MSCs in both growth medium and osteogenic medium. However, Metformin, another AMPK activator, showed no such effects. Meanwhile, AICAR significantly inhibited adipogenic differentiation of hAMSCs and BM-MSCs. Our data suggests that AICAR represents a potent molecule, which can be applied in bone tissue regeneration.
引用
收藏
页码:1128 / 1136
页数:9
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