Origin, prospective identification, and function of circulating endothelial colony-forming cells in mice and humans.

Origin, prospective identification, and function of circulating endothelial colony-forming cells in mice and humans.
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DOI:
10.1172/jci.insight.164781
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发表时间:
2023-03-08
期刊:
影响因子:
8
通讯作者:
Yoder, Mervin C. .
Yoder, Mervin C. .
中科院分区:
医学1区
文献类型:
--
作者:
Lin, Yang;Banno, Kimihiko;Gil, Chang-Hyun;Myslinski, Jered;Hato, Takashi;Shelley, William C. .;Gao, Hongyu;Xuei, Xiaoling;Liu, Yunlong;Basile, David P. .;Yoshimoto, Momoko;Prasain, Nutan;Tarnawsky, Stefan P.;Adams, Ralf H.;Naruse, Katsuhiko;Yoshida, Junko;Murphy, Michael P. .;Horie, Kyoji;Yoder, Mervin C. .

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Most circulating endothelial cells are apoptotic, but rare circulating endothelial colony-forming cells (C-ECFCs), also known as blood outgrowth endothelial cells, with proliferative and vasculogenic activity can be cultured; however, the origin and naive function of these C-ECFCs remains obscure. Herein, detailed lineage tracing revealed murine C-ECFCs emerged in the early postnatal period, displayed high vasculogenic potential with enriched frequency of clonal proliferative cells compared with tissue-resident ECFCs, and were not committed to or derived from the BM hematopoietic system but from tissue-resident ECFCs. In humans, C-ECFCs were present in the CD34bright cord blood mononuclear subset, possessed proliferative potential and in vivo vasculogenic function in a naive or cultured state, and displayed a single cell transcriptome sharing some umbilical venous endothelial cell features, such as a higher protein C receptor and extracellular matrix gene expression. This study provides an advance for the field by identifying the origin, naive function, and antigens to prospectively isolate C-ECFCs for translational studies.
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