4.6 Article

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

Journal

AGING-US
Volume 13, Issue 19, Pages 22985-23003

Publisher

IMPACT JOURNALS LLC

Keywords

browning; skeletal muscle; FEYE; proliferation and differentiation; VTG2

Funding

  1. Key R&D Projects in Shanxi Province [201803D221022-2]
  2. Scientific and Technological Innovation Project for Excellent Talents in Shanxi Province [201805D211012]
  3. National Natural Science Foundation of China [31772690]
  4. Fund Program for the Scientific Activities of Selected Returned Overseas Professionals in Shanxi Province
  5. Young Science Foundation of Shanxi Province [201901D211368]
  6. Fund for Shanxi 1331 Project [20211331-16, 20211331-13]

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Recent study showed that fertilized egg yolk extract (FEYE) can promote skeletal muscle development by inhibiting the expression of muscle atrophy genes, and stimulate the browning reaction of white adipocytes.
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.

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