Upregulation of FNDC5 gene expression in C2C12 cells after single and combined treatments of resveratrol and ATRA

被引:10
作者
Abedi-Taleb, Elahe [1 ]
Vahabi, Zahra [2 ,3 ]
Sekhavati-Moghadam, Ehsan [4 ]
Khedmat, Leila [5 ]
Jazayeri, Shima [6 ]
Saboor-Yaraghi, Ali Akbar [1 ,7 ]
机构
[1] Univ Tehran Med Sci, Sch Nutr Sci & Dietet, Dept Cellular & Mol Nutr, Tehran, Iran
[2] Univ Tehran Med Sci, Ziaeian Hosp, Dept Geriatr Med, Tehran, Iran
[3] Univ Tehran Med Sci, Roozbeh Hosp, Memory & Behav Neurol Div, Tehran, Iran
[4] Univ Tehran Med Sci, Ziaeian Hosp, Dept Cardiol, Tehran, Iran
[5] Baqiyatallah Univ Med Sci, Hlth Management Res Ctr, Tehran, Iran
[6] Iran Univ Med Sci, Sch Publ Hlth, Dept Nutr & Biochem, Tehran, Iran
[7] Univ Tehran Med Sci, Sch Publ Hlth, Dept Immunol, Tehran 141613151, Iran
关键词
FNDC5; Thermogenesis; Retinoic acid; Resveratrol; CIRCULATING IRISIN LEVELS; SKELETAL-MUSCLE; ENERGY-EXPENDITURE; ADIPOSE-TISSUE; METABOLISM; OBESITY; DIFFERENTIATION; ASSOCIATION; MYOKINE; MICE;
D O I
10.1186/s12944-019-1128-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background Irisin is a newly discovered myokine that secreted from skeletal muscle cells. Several studies showed that irisin involves in thermogenesis and increases the expression of browning markers such as uncoupling protein-1 that in turns induces the conversion of white adipose tissue to brown fat. Resveratrol (Res) and all-trans retinoic acid (ATRA) can also upregulate the expression of thermogenesis genes. In the present study, the effects of single and combined treatments of Res and ATRA on fibronectin type III domain containing 5 (FNDC5) gene expression was explored. Methods The mouse myoblasts, C2C12 cells, were seeded in 6-well plastic plates and cultured in DMEM media. After differentiation, in a pilot study, C2C12 myotubes were treated with different concentrations of Res and ATRA for 12 h. The best result was obtained by treatment of 1and 25 mu M of Res and 1 mu M of ATRA. Then the main study was continued by single and combined treatment of these compounds at chosen concentration. After treatments, total RNA was extracted from C2C12 cells. Complementary DNA (cDNA) was generated by the cDNA synthesis kit and FNDC5 mRNA expression was evaluated by the real-time PCR method. Results The FNDC5 gene expression in C2C12 myotubes of alone-treated with 1 mu M, 25 mu M Res and 10 mu M ATRA did not change compared to vehicle group. However, in combination-treated the expression of FNDC5 gene was significantly increased compared to vehicle group. Conclusion This is the first evidence that Res and ATRA can regulate FNDC5 gene expression in C2C12 myotubes. More investigations are necessary to explore the therapeutic effects of these nutrients in obesity, diabetes, cardiac and neurovascular disease.
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页数:6
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