Vitellogenin 2 promotes muscle development and stimulates the browning of white fat

被引:0
|
作者
Li, Yilei [1 ]
Sun, Xiaoli [2 ]
Bai, Yun [1 ]
Ji, Yunyan [1 ]
Ren, Huawei [1 ]
Yu, Xiuju [1 ]
Yan, Yi [1 ]
He, Xiaoyan [1 ]
Dong, Yanjun [3 ]
Zhang, Liping [1 ,4 ]
Luo, Xiaomao [1 ]
Wang, Haidong [1 ]
机构
[1] Shanxi Agr Univ, Coll Vet Med, Taigu 030801, Shanxi, Peoples R China
[2] Tongji Univ, Shanghai Pulm Hosp, Dept Resp & Crit Care Med, Sch Med, Shanghai 200433, Peoples R China
[3] China Agr Univ, Coll Vet Med, Beijing 100193, Peoples R China
[4] Baylor Coll Med, Dept Med, Nephrol Div, Houston, TX 77030 USA
来源
AGING-US | 2021年 / 13卷 / 19期
基金
中国国家自然科学基金;
关键词
browning; skeletal muscle; FEYE; proliferation and differentiation; VTG2; ACTIVIN RECEPTOR IIB; SKELETAL-MUSCLE; ADIPOSE-TISSUE; MYOSTATIN; PROTEIN; IRISIN; GROWTH; GENE; DIFFERENTIATION; THERMOGENESIS;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Eggs are rich in nutrients and contain a lot of protein. Although eggs have proved to accelerate the growth of C2C12 cells, the regulatory and mechanism of fertilized egg yolk extract (FEYE) on skeletal muscle development and fat metabolism remains unclearly. The mice were treated with FEYE by gavage for 24 d, we found that FEYE can inhibit the expression of skeletal muscle atrophy genes such as MSTN and Murf-1, and up-regulate the expression levels of MYOD, MYOG and Irisin. In addition, the treatment of FEYE induced UCP1 and PGC1a high expression in WAT, thereby causing WAT browning reaction. In order to confirm the composition of FEYE, we performed protein full spectrum identification (LC MS/MS) analysis and found the most enriched component is vitellogenin 2 (VTG2). Therefore, we added the recombinant protein VTG2 to C2C12 cells and found that VTG2 promoted the proliferation and differentiation of C2C12 cells. After that, we further proved that VTG2 inhibited the expression of MSTN and improved the expression of MYOD and Irisin. Finally, the dual luciferase test proved that VTG2 directly inhibited the transcriptional activity of MSTN. Our results conclude that FEYE inhibits the expression of MSTN in muscle tissues by delivering VTG2, thereby promoting skeletal muscle development, and can also promote the expression level of FNDC5 in serum. Then, FNDC5 acts on the fat through the serum, stimulating the browning reaction of white adipocytes. Therefore, VTG2 can be used to stop muscle consumption, improve skeletal muscle aging, and prevent obesity.
引用
收藏
页码:22985 / 23003
页数:19
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