JAGGED1 Signaling Regulates Hemangioma Stem Cell–to–Pericyte/Vascular Smooth Muscle Cell Differentiation
Author(s) -
Elisa Boscolo,
Camille L. Stewart,
Shoshana Greenberger,
June K. Wu,
Jennifer T. Durham,
Ira M. Herman,
John B. Mulliken,
Jan Kitajewski,
Joyce Bischoff
Publication year - 2011
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.111.232934
Subject(s) - pericyte , vascular smooth muscle , microbiology and biotechnology , stem cell , cell , cellular differentiation , endothelial stem cell , biology , signal transduction , smooth muscle , pathology , anatomy , medicine , endocrinology , biochemistry , gene , in vitro
Objective— The aim of our study is to determine the cellular and molecular origin for the pericytes in infantile hemangioma (IH) and their functional role in the formation of pathological blood vessels. Methods and Results— Here we show that IH-derived stem cells (HemSCs) form pericyte-like cells. With in vitro studies, we demonstrate that HemSC-to-pericyte differentiation depends on direct contact with endothelial cells. JAGGED1 expressed ectopically in fibroblasts was sufficient to induce HemSCs to acquire a pericyte-like phenotype, indicating a critical role for JAGGED1. In vivo, we blocked pericyte differentiation with recombinant JAGGED1, and we observed reduced formation of blood vessels, with an evident lack of pericytes. SilencingJAGGED1 in the endothelial cells reduced blood vessel formation and resulted in a paucity of pericytes.Conclusion— Our data show that endothelial JAGGED1 controls HemSC-to-pericyte differentiation in a murine model of IH and suggests that pericytes have a fundamental role in formation of blood vessels in IH.
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