Prospective identification of myogenic endothelial cells in human skeletal muscle

被引:250
作者
Zheng, Bo
Cao, Baohong
Crisan, Mihaela
Sun, Bin
Li, Guangheng
Logar, Alison
Yap, Solomon
Pollett, Jonathan B.
Drowley, Lauren
Cassino, Theresa
Gharaibeh, Burhan
Deasy, Bridget M.
Huard, Johnny
Peault, Bruno
机构
[1] Childrens Hosp Pittsburgh, Stem Cell Res Ctr, Dept Orthopaed Surg, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Pediat, Pittsburgh, PA USA
[3] Univ Pittsburgh, Inst Canc, Pittsburgh, PA USA
[4] Univ Pittsburgh, Sch Med, Childrens Hosp, Dept Mol Genet & Biochem, Pittsburgh, PA USA
[5] Univ Pittsburgh, Sch Med, Childrens Hosp, Dept Bioengn, Pittsburgh, PA USA
[6] Univ Pittsburgh, Sch Med, Childrens Hosp, McGowan Inst Regenerat Med, Pittsburgh, PA USA
关键词
D O I
10.1038/nbt1334
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We document anatomic, molecular and developmental relationships between endothelial and myogenic cells within human skeletal muscle. Cells coexpressing myogenic and endothelial cell markers (CD56, CD34, CD144) were identified by immunohistochemistry and flow cytometry. These myoendothelial cells regenerate myofibers in the injured skeletal muscle of severe combined immunodeficiency mice more effectively than CD56(+) myogenic progenitors. They proliferate long term, retain a normal karyotype, are not tumorigenic and survive better under oxidative stress than CD56(+) myogenic cells. Clonally derived myoendothelial cells differentiate into myogenic, osteogenic and chondrogenic cells in culture. Myoendothelial cells are amenable to biotechnological handling, including purification by flow cytometry and long-term expansion in vitro, and may have potential for the treatment of human muscle disease.
引用
收藏
页码:1025 / 1034
页数:10
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