Related Experiment Video
Updated: Mar 29, 2026

07:51
Preparation of Primary Myogenic Precursor Cell/Myoblast Cultures from Basal Vertebrate Lineages
Published on: April 30, 2014
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PDGFD: A Dual-Function Regulator That Maintains Myoblast Pool and Fuels Myogenic Differentiation
Hongzhen Cao1, Jing Wang2, Yunzhou Wang3
1Shandong Provincial Key Laboratory for Livestock Germplasm Innovation & Utilization, College of Animal Science and Technology, Shandong Agricultural University, Tai'an 271018, China.
Current Issues in Molecular Biology
|March 28, 2026
Summary
Platelet-derived growth factor D (PDGFD) maintains the myoblast pool and initiates muscle cell differentiation. This study reveals PDGFD
Area of Science:
- Muscle biology
- Cellular signaling
- Developmental biology
Background:
- The function of platelet-derived growth factor D (PDGFD) in mesenchymal cells is known, but its role in skeletal muscle generation is unclear.
- PDGFD is identified as a candidate gene for muscle and fat development in pigs.
Purpose of the Study:
- To elucidate the specific role of PDGFD in skeletal muscle generation and myogenesis.
- To investigate the regulatory mechanisms of PDGFD in myoblast proliferation, apoptosis, and differentiation.
Main Methods:
- Single-cell RNA sequencing of skeletal muscle from Jiangquan Black pigs.
- C2C12 cell line experiments involving PDGFD knockdown and overexpression.
- Analysis of myogenic differentiation markers (MyoD, MyoG) and signaling pathways (PI3K/Akt).
Main Results:
- PDGFD knockdown inhibited proliferation and promoted apoptosis in myoblasts; overexpression enhanced viability.
- PDGFD interference downregulated MyoD and MyoG, inhibiting myogenic differentiation.
- PDGFD expression peaks during mid-differentiation, suggesting temporal regulation, potentially via a pathway independent of PI3K/Akt.
Conclusions:
- PDGFD plays a dual role in myogenesis, acting as both a guardian of the myoblast pool and an initiator of differentiation.
- This study expands the known functions of PDGFD and provides novel insights into growth factor-mediated cell fate decisions in muscle development.
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