Identification of myosin II as a cripto binding protein and regulator of cripto function in stem cells and tissue
Malachia Hoover1, Farhana Runa1, Evan Booker2
1Department of Biology, California State University Northridge, USA.
Abstract:
Cripto regulates stem cell function in normal and disease contexts via TGFbeta/activin/nodal, PI3K/Akt, MAPK and Wnt signaling. Still, the molecular mechanisms that govern these pleiotropic functions of Cripto remain poorly understood. We performed an unbiased screen for novel Cripto binding proteins using proteomics-based methods, and identified novel proteins including members of myosin II complexes, the actin cytoskeleton, the cellular stress response, and extracellular exosomes. We report that myosin II, and upstream ROCK1/2 activities are required for localization of Cripto to cytoplasm/membrane domains and its subsequent release into the conditioned media fraction of cultured cells. Functionally, we demonstrate that soluble Cripto (one-eyed pinhead in zebrafish) promotes proliferation in mesenchymal stem cells (MSCs) and stem cell-mediated wound healing in the zebrafish caudal fin model of regeneration. Notably, we demonstrate that both Cripto and myosin II inhibitors attenuated regeneration to a similar degree and in a non-additive manner. Taken together, our data present a novel role for myosin II function in regulating subcellular Cripto localization and function in stem cells and an important regulatory mechanism of tissue regeneration. Importantly, these insights may further the development of context-dependent Cripto agonists and antagonists for therapeutic benefit.
Insights
Cripto protein
Area of Science:
- Molecular Biology
- Cell Biology
- Developmental Biology
Background:
- Cripto is a key regulator of stem cell function through multiple signaling pathways.
- The precise molecular mechanisms underlying Cripto's diverse roles are not fully understood.
Purpose of the Study:
- To identify novel Cripto-interacting proteins and elucidate Cripto's regulatory mechanisms in stem cells and tissue regeneration.
Main Methods:
- Unbiased proteomics screen to identify Cripto binding proteins.
- Cellular localization studies and functional assays in mesenchymal stem cells (MSCs).
- Zebrafish caudal fin regeneration model to assess Cripto's role in vivo.
Main Results:
- Myosin II and ROCK1/2 kinases are identified as novel Cripto-interacting proteins, regulating its localization and release.
- Soluble Cripto enhances MSC proliferation and promotes stem cell-mediated wound healing in zebrafish.
- Inhibition of Cripto or myosin II similarly impairs zebrafish fin regeneration.
Conclusions:
- Myosin II plays a critical role in controlling Cripto's subcellular localization and function in stem cells.
- This study reveals a novel mechanism regulating Cripto's involvement in tissue regeneration.
- Findings may inform the development of Cripto-based therapeutics for regenerative medicine.
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