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Enhancing the Engraftment of Human Induced Pluripotent Stem Cell-derived Cardiomyocytes via a Transient Inhibition of Rho Kinase Activity
Published on: July 10, 2019
PP2A regulates SCF-induced cardiac stem cell migration through interaction with p38 MAPK.
Ying Wang1, Yanli Xia1, Dong Kuang2
1Institute of Pathology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, PR China; Department of Pathology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, PR China.
Protein phosphatase 2A (PP2A) regulates cardiac stem cell (CSC) migration induced by stem cell factor (SCF). PP2A inactivation by p38 MAPK enhances SCF-induced CSC migration and signaling.
Area of Science:
- Cardiovascular Biology
- Cell Signaling
- Stem Cell Research
Background:
- Stem cell factor (SCF) promotes cardiac stem cell (CSC) migration and myocardial infarction repair.
- Previous migration studies focused on kinase activation, neglecting phosphatase roles.
Purpose of the Study:
- To investigate the role of protein phosphatase 2A (PP2A) in SCF-induced CSC migration.
- To elucidate the mechanism of PP2A involvement in CSC migration.
Main Methods:
- Cardiac stem cells (CSCs) were treated with SCF.
- Western blot analyzed phosphorylation of PP2A, p38 MAPK, and cofilin.
- Transwell assays assessed CSC migratory ability.
- PP2A activity and interactions were evaluated.
Main Results:
- SCF induced CSC migration via p38 MAPK and cofilin phosphorylation.
- PP2A was inactivated by SCF through p38 MAPK-mediated phosphorylation at Tyr307.
- PP2A inhibition enhanced SCF-induced migration, while p38 MAPK blockade reversed this.
- PP2A directly interacts with p38 MAPK.
Conclusions:
- PP2A regulates SCF-induced CSC migration.
- PP2A interacts with p38 MAPK to modulate the p38 MAPK/cofilin signaling pathway.
- This interaction is crucial for CSC migration in response to SCF.
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