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Morphogenetic Sphingolipids in Stem Cell Differentiation and Embryo Development

Producción científica: Chapterrevisión exhaustiva

4 Citas (Scopus)

Resumen

The lipid composition in stem cells undergoes remarkable changes during neural differentiation. Growing evidence suggests that lipids regulate stem cell differentiation through three mechanisms: direct binding and regulation of lipid-specific receptors, regulation of non-lipid receptors by clustering with lipids in microdomains or rafts, and enrichment of specific lipids in compartments and vesicles. Lipid-driven compartmentalization is critical for vesicle trafficking, cell polarity and ultimately, embryo development. Sphingolipids such as ceramide are strictly compartmentalized to function in distinct differentiation programs. Research in our laboratory has focused on the function of ceramide-enriched compartments (CECs). Ceramide and its derivative, sphingosine-1-phosphate (S1P), are counteractive in stem cell apoptosis vs. survival, but they can act synergistically in neural progenitor cell differentiation. This review discusses studies on lipid-induced stem cell differentiation and embryo development with focus on sphingolipids as “morphogenetic lipids” and potential drug targets in regenerative medicine.

Idioma originalEnglish
Título de la publicación alojadaStem Cell Biology and Regenerative Medicine
Páginas11-40
Número de páginas30
DOI
EstadoPublished - 2017

Serie de la publicación

NombreStem Cell Biology and Regenerative Medicine
VolumenPart F4899
ISSN (versión impresa)2196-8985
ISSN (versión digital)2196-8993

Nota bibliográfica

Publisher Copyright:
© Springer International Publishing AG 2017.

Financiación

Acknowledgments This study was supported by grants NIH R01AG034389, R01NS095215, and NSF1121579 to E.B. and American Lung Association RG-351596 to G.W.W e are also grateful to institutional support by the Department of Neuroscience and Regenerative Medicine (chair Dr. Lin Mei), Medical College of Georgia at Augusta University.

FinanciadoresNúmero del financiador
Department of Neuroscience and Regenerative Medicine
Augusta University
National Institutes of Health (NIH)R01NS095215, R01AG034389, NSF1121579
American Lung AssociationRG-351596

    ASJC Scopus subject areas

    • Cell Biology
    • Molecular Medicine

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