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Published on: May 17, 2016
Xk-related protein 8 regulates myoblast differentiation and survival
Go-Woon Kim1, Gi-Hoon Nam1,2, In-San Kim1,2
1Center for Theragnosis, Biomedical Research Institute, Korea Institute of Science and Technology (KIST), Seoul, Korea.
Abstract:
Xk-related protein 8 (Xkr8) is a scramblase and responsible for phosphatidylserine (PS) exposure on the cell surface in a caspase-dependent manner. Although PS exposure is found to be important for myotube formation during myoblast differentiation, the role of Xkr8 during myogenesis has not been elucidated. Here we show that Xkr8 contributes to myoblast differentiation. Xkr8 overexpression induced the formation of large myotubes during early differentiation, but this phenotype was not related to caspase-dependent cleavage of Xkr8. Furthermore, forced Xkr8 expression accelerated myoblast differentiation and conferred cell-death resistance after the induction of differentiation. Consistent with these results, Xkr8-knocked-down myoblasts exhibited impaired differentiation and more apoptotic cells during differentiation, implying the involvements of Xkr8 in the survival and proliferation of myoblasts. Taken together, the study shows Xkr8 influences myogenesis by acting as a positive regulator of terminal differentiation and myoblast survival.
Insights
Xk-related protein 8 (Xkr8) promotes muscle cell (myoblast) differentiation and survival. This protein enhances myotube formation and protects cells during differentiation, indicating its crucial role in myogenesis.
Area of Science:
- Cell Biology
- Muscle Development
Background:
- Phosphatidylserine (PS) exposure is critical for myotube formation during myoblast differentiation.
- The specific role of Xk-related protein 8 (Xkr8), a PS scramblase, in myogenesis remained unclear.
Discussion:
- Xkr8 overexpression accelerates myoblast differentiation and promotes the formation of larger myotubes.
- This pro-myogenic effect of Xkr8 is independent of caspase-dependent cleavage.
- Xkr8 enhances cell-death resistance in differentiated myoblasts.
Key Insights:
- Xkr8 acts as a positive regulator in terminal differentiation and myoblast survival.
- Xkr8 knockdown impairs myoblast differentiation and increases apoptosis during differentiation.
- Xkr8 influences myoblast proliferation and survival, impacting overall myogenesis.
Outlook:
- Further research into Xkr8's non-caspase-dependent functions in myogenesis.
- Investigating Xkr8's potential as a therapeutic target for muscle-related disorders.
- Elucidating the precise molecular mechanisms by which Xkr8 regulates myoblast survival and proliferation.
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