The L-Ascorbic Acid Increases Proliferation and Differentiation of Yanbian Cattle Skeletal Muscle Satellite Cells by Activating the Akt/mTOR/P70S6K Signaling Pathway

被引:0
|
作者
Jin, Huaina [1 ]
Li, Qiang [1 ]
Tang, Lin [1 ]
Naseem, Sajida [1 ]
Park, Sungkwon [2 ]
Wang, Enze [1 ]
Sun, Bin [1 ]
Manzoor, Abid [1 ]
Hur, Sun Jin [3 ]
Li, Xiangzi [1 ]
Choi, Seong-Ho [4 ]
机构
[1] Yanbian Univ, Engn Res Ctr North East Cold Reg Beef Cattle Sci &, Dept Anim Sci, Minist Educ, Yanji 133002, Peoples R China
[2] Sejong Univ, Dept Food Sci & Biotechnol, Seoul 05006, South Korea
[3] Chung Ang Univ, Dept Anim Sci & Technol, Anseong 17546, South Korea
[4] Chungbuk Natl Univ, Dept Anim Sci, Cheongju 28644, South Korea
基金
中国国家自然科学基金;
关键词
cell proliferation; cell differentiation; L-ascorbic acid; rapamycin pathway; skeletal muscle satellite cells; VITAMIN-C; 2-PHOSPHATE; EXPRESSION;
D O I
10.5851/kosfa.2024.e50
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Cell-cultured meat, as a new type of meat food, can effectively mitigate the negative effects of conventional animal husbandry on the environment, health, and animal welfare. Muscle stem cells are the main seed cells for the production of cell- cultured meat, but their weak proliferative capacity in vitro severely limits the large-scale and low-cost production of cell-cultured meat. There is growing evidence that L-ascorbic acid (AA) has the ability to increase the efficiency of muscle stem cell proliferation and differentiation in vitro. However, the role of AA in Yanbian bovine skeletal muscle satellite cells (BSCs) and its molecular mechanisms are unknown. Therefore, in the present study, the promotional effect of AA on the proliferation and differentiation of BSCs was confirmed by the Cell Counting Kit 8 (CCK-8) assay, 5-ethyl-2 '-deoxyuridine (EdU) proliferation assay, real-time quantitative PCR (RT-qPCR), immunoprotein blotting (Western blotting) and immunofluorescence assay. RT-qPCR and Western blotting results showed that AA up-regulated the expression of p-Akt, p-mTOR, and pP70S6K genes and proteins, whereas when the mTOR pathway inhibitor rapamycin was co-treated with AA in BSCs, the expression of p-Akt, p-mTOR, and p-P70S6K genes and proteins was significantly down-regulated. In summary, data suggest that AA regulates the proliferation and differentiation of BSCs by activating the AKT/mTOR/P70S6K signaling pathway. These data provide a practical approach and theoretical basis for the efficient and low-cost manufacture of cell culture meat.
引用
收藏
页码:484 / 503
页数:20
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