| Literature DB >> 29429943 |
Taku Wakabayashi1, Hisamichi Naito2, Jun-Ichi Suehiro3, Yang Lin4, Hideya Kawaji5, Tomohiro Iba6, Tsukasa Kouno7, Sachi Ishikawa-Kato7, Masaaki Furuno7, Kazuhiro Takara6, Fumitaka Muramatsu6, Jia Weizhen6, Hiroyasu Kidoya6, Katsuhiko Ishihara8, Yoshihide Hayashizaki9, Kohji Nishida10, Mervin C Yoder4, Nobuyuki Takakura11.
Abstract
The generation of new blood vessels via angiogenesis is critical for meeting tissue oxygen demands. A role for adult stem cells in this process remains unclear. Here, we identified CD157 (bst1, bone marrow stromal antigen 1) as a marker of tissue-resident vascular endothelial stem cells (VESCs) in large arteries and veins of numerous mouse organs. Single CD157+ VESCs form colonies in vitro and generate donor-derived portal vein, sinusoids, and central vein endothelial cells upon transplantation in the liver. In response to injury, VESCs expand and regenerate entire vasculature structures, supporting the existence of an endothelial hierarchy within blood vessels. Genetic lineage tracing revealed that VESCs maintain large vessels and sinusoids in the normal liver for more than a year, and transplantation of VESCs rescued bleeding phenotypes in a mouse model of hemophilia. Our findings show that tissue-resident VESCs display self-renewal capacity and that vascular regeneration potential exists in peripheral blood vessels.Entities:
Keywords: CD157; angiogenesis; endothelial colony-forming cell; hemophilia; side population; vascular endothelial stem cells; vascular regeneration
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Year: 2018 PMID: 29429943 DOI: 10.1016/j.stem.2018.01.010
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633