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J. Dev. Biol. 2015, 3(4), 112-128; doi:10.3390/jdb3040112

Pigment Epithelium-Derived Factor (PEDF) is a Determinant of Stem Cell Fate: Lessons from an Ultra-Rare Disease

1
Department of Medicine, Yale University School of Medicine, New Haven, CT 06510, USA
2
VA CT Healthcare System, West Haven, CT 06516, USA
*
Author to whom correspondence should be addressed.
Academic Editors: Robert W. Dettman and Andy Wessels
Received: 17 October 2015 / Accepted: 16 November 2015 / Published: 20 November 2015
(This article belongs to the Special Issue Cell Fate Decisions in Development and Disease)
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Abstract

PEDF is a secreted glycoprotein that is widely expressed by multiple organs. Numerous functional contributions have been attributed to PEDF with antiangiogenic, antitumor, anti-inflammatory, and neurotrophic properties among the most prominent. The discovery that null mutations in the PEDF gene results in Osteogenesis Imperfecta Type VI, a rare autosomal recessive bone disease characterized by multiple fractures, highlights a critical developmental function for this protein. This ultra-rare orphan disease has provided biological insights into previous studies that noted PEDF’s effects on various stem cell populations. In addition to bone development, PEDF modulates resident stem cell populations in the brain, muscle, and eye. Functional effects on human embryonic stem cells have also been demonstrated. An overview of recent advances in our understanding by which PEDF regulates stem cells and their potential clinical applications will be evaluated in this review. View Full-Text
Keywords: pigment epithelium-derived factor; osteogenesis imperfecta; stem cells; Wnt signaling pigment epithelium-derived factor; osteogenesis imperfecta; stem cells; Wnt signaling
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MDPI and ACS Style

Sagheer, U.; Gong, J.; Chung, C. Pigment Epithelium-Derived Factor (PEDF) is a Determinant of Stem Cell Fate: Lessons from an Ultra-Rare Disease. J. Dev. Biol. 2015, 3, 112-128.

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