| Literature DB >> 31840004 |
Charles Hwang1, Simone Marini1,2, Amanda K Huber1, David M Stepien1, Michael Sorkin1, Shawn Loder1, Chase A Pagani1, John Li1, Noelle D Visser1, Kaetlin Vasquez1, Mohamed A Garada1, Shuli Li1, Jiajia Xu3, Ching-Yun Hsu3, Paul B Yu4, Aaron W James3, Yuji Mishina5, Shailesh Agarwal1, Jun Li2, Benjamin Levi1.
Abstract
Heterotopic ossification (HO) is a debilitating condition characterized by the pathologic formation of ectopic bone. HO occurs commonly following orthopedic surgeries, burns, and neurologic injuries. While surgical excision may provide palliation, the procedure is often burdened with significant intra-operative blood loss due to a more robust contribution of blood supply to the pathologic bone than to native bone. Based on these clinical observations, we set out to examine the role of vascular signaling in HO. Vascular endothelial growth factor A (VEGFA) has previously been shown to be a crucial pro-angiogenic and pro-osteogenic cue during normal bone development and homeostasis. Our findings, using a validated mouse model of HO, demonstrate that HO lesions are highly vascular, and that VEGFA is critical to ectopic bone formation, despite lacking a contribution of endothelial cells within the developing anlagen.Entities:
Keywords: Bone; Pathogenesis
Year: 2019 PMID: 31840004 PMCID: PMC6904752 DOI: 10.1038/s41413-019-0075-6
Source DB: PubMed Journal: Bone Res ISSN: 2095-4700 Impact factor: 13.567