| Literature DB >> 31721342 |
Lijun Ding1,2,3, Bianca Vezzani2,4, Nusrat Khan2, Jing Su1, Lu Xu1, Guijun Yan1, Yong Liu5, Ruotian Li6, Anushri Gaur2, Zhenyu Diao1, Yali Hu1, Zhongzhou Yang7, W Reef Hardy8, Aaron W James8,9, Haixiang Sun1,10, Bruno Péault2,8.
Abstract
The tunica adventitia ensheathes arteries and veins and contains presumptive mesenchymal stem cells (MSCs) involved in vascular remodeling. We show here that a subset of human adventitial cells express the CD10/CALLA cell surface metalloprotease. Both CD10+ and CD10- adventitial cells displayed phenotypic features of MSCs when expanded in culture. However, CD10+ adventitial cells exhibited higher proliferation, clonogenic and osteogenic potentials in comparison to their CD10- counterparts. CD10+ adventitial cells increased expression of the cell cycle protein CCND2 via ERK1/2 signaling and osteoblastogenic gene expression via NF-κB signaling. CD10 expression was upregulated in adventitial cells through sonic hedgehog-mediated GLI1 signaling. These results suggest that CD10, which marks rapidly dividing cells in other normal and malignant cell lineages, plays a role in perivascular MSC function and cell fate specification. These findings also point to a role for CD10+ perivascular cells in vascular remodeling and calcification. ©AlphaMed Press 2019.Entities:
Keywords: CD10; GLI1; SHH; adventitia; mesenchymal stem cell; osteogenesis; vascular calcification
Mesh:
Substances:
Year: 2019 PMID: 31721342 DOI: 10.1002/stem.3112
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277