Cordycepin protected against the TNF--induced inhibition of osteogenic differentiation of human adipose-derived mesenchymal stem cells

被引:17
作者
Yang, Jianping [1 ,3 ]
Cao, Yan [2 ]
Lv, Zhengxiang [3 ]
Jiang, Tao [3 ]
Wang, Liming [1 ]
Li, Zhong [4 ]
机构
[1] Nanjing Med Univ, Nanjing Hosp 1, Dept Orthopaed, Nanjing 210012, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Changzhou Peoples Hosp 2, Dept Dermatol, Changzhou 213003, Peoples R China
[3] Nanjing Univ Tradit Chinese Med, Dept Orthopaed, Changzhou Tradit Chinese Med Hosp, Changzhou 213000, Peoples R China
[4] Nanjing Med Univ, Sch Publ Hlth, Minist Educ, Dept Nutr & Food Hyg,Key Lab Modern Toxicol, Nanjing 211166, Jiangsu, Peoples R China
关键词
adipose-derived mesenchymal stem cells; bone diseases; cordycepin; inflammation; TUMOR-NECROSIS-FACTOR; OSTEOBLAST DIFFERENTIATION; IN-VITRO; FACTOR-ALPHA; BONE-MARROW; INFLAMMATION; REGULATOR; PATHWAYS; RECEPTOR; MODEL;
D O I
10.1177/0394632015592160
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cordycepin, 3'-deoxyadenosine, is an effective component isolated from the rare Chinese caterpillar fungus Cordyceps militaris. It exerts potent anti-inflammatory actions in different cell and animal models. However, its action remains unclear on the TNF--induced inhibition of osteogenic differentiation of adipose-derived mesenchymal stem cells (ADMSCs). In the present study, we demonstrated that cordycepin induced cell death at 20 and 40 g/mL. Interestingly, 10 g/mL cordycepin abrogated the cell death induced by 20 ng/mL TNF-. Meanwhile, cordycepin exhibited a dose-dependent regulation of the osteogenesis of human ADMSCs: it promoted the differentiation at 10 g/mL, whereas inhibited differentiation at 40 g/mL. Furthermore, we discovered that 10 g/mL cordycepin protected against the TNF- (induced inhibition of osteogenic differentiation of human ADMSCs. It was also revealed that 10 g/mL cordycepin restored Runx2 and Osx mRNA levels, which were significantly inhibited by TNF-during osteogenesis. At the same time, we found that 10 g/mL cordycepin suppressed TNF--activated NF-B signaling, by inhibiting IB phosphorylation and subsequent p65 release and translocation into the cell nucleus. Of clinical interest, the present study revealed mechanisms involved in inflammatory cytokine-inhibited osteogenesis, and it highlights the potential of cordycepin to promote the osteogenesis of human ADMSCs in cell-based therapy for inflammatory bone diseases.
引用
收藏
页码:296 / 307
页数:12
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