Por favor, use este identificador para citar o enlazar este ítem: 10.14670/HH-11-598

Título: The pivotal role of PDGF and its receptor isoforms in adipose-derived stem cells
Fecha de publicación: 2015
Editorial: Universidad de Murcia. Servicio de publicaciones
Cita bibliográfica: Histology and Histopathology, vol. 30, nº 7, (2015)
ISSN: 1699-5848
Materias relacionadas: CDU::6 - Ciencias aplicadas::61 - Medicina::616 - Patología. Medicina clínica. Oncología
Palabras clave: Adipose-derived stem cells
Platelet-derived growth factor
Receptor
Reactive oxygen species
Mitogenic effect
Resumen: Platelet-derived growth factor (PDGF) is one of the growth factors that reportedly regulates cell growth and division of mesenchymal cells. Although PDGF isoforms and their receptors reportedly play a pivotal role in mesenchymal stem cell regulation, there is a paucity of literature reviewing the role of PDGF in adipose-derived stem cells (ASCs). Therefore, we summarized previous reports on the expression and functional roles of PDGF and its receptor isoforms in this review. In addition, we examined findings pertaining to underlying molecular mechanisms and signaling pathways with special focus on PDGF-D/PDGFRβ. ASCs only express PDGF-A, -C, -D, PDGFRα, and PDGFRβ. PDGFRα expression decreases with adipocyte lineage, while PDGFRβ inhibits white adipocyte differentiation. In addition, PDGFRβ induces proliferation, migration, and angiogenesis and upregulates the expression of paracrine factors in ASCs. Although PDGF-B and -D mediate their functions mainly by PDGFRβ and ROS generation, there are many differences between them in terms of regulating ASCs. PDGF-D is endogenous, generates ROS via the mitochondrial electron transport system, and regulates the autocrine loop of ASCs in vivo. Furthermore, PDGFD has stronger mitogenic effects than PDGF-B.
Autor/es principal/es: Kim, Won-Serk
Park, Hyoung-Sook
Sung, Jong-Hyuk
URI: http://hdl.handle.net/10201/96485
DOI: 10.14670/HH-11-598
Tipo de documento: info:eu-repo/semantics/article
Número páginas / Extensión: 7
Derechos: info:eu-repo/semantics/openAccess
Attribution-NonCommercial-NoDerivatives 4.0 International
Aparece en las colecciones:Vol.30, nº7 (2015)

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