Specification and Diversification of Pericytes and Smooth Muscle Cells from Mesenchymoangioblasts.
Specification and Diversification of Pericytes and Smooth Muscle Cells from Mesenchymoangioblasts.
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DOI:
10.1016/j.celrep.2017.05.019
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发表时间:
2017-05-30
期刊:
影响因子:
8.8
通讯作者:
Slukvin II
中科院分区:
文献类型:
--
作者:
Kumar A;D'Souza SS;Moskvin OV;Toh H;Wang B;Zhang J;Swanson S;Guo LW;Thomson JA;Slukvin II
Elucidating the pathways that lead to vasculogenic cells, and being able to identify their progenitors and lineage-restricted cells, is critical to the establishment of human pluripotent stem cell (hPSC) models for vascular diseases and development of vascular therapies. Here, we find that mesoderm-derived pericytes (PCs) and smooth muscle cells (SMCs) originate from a clonal mesenchymal progenitor mesenchymoangioblast (MB). In clonogenic cultures, MBs differentiate into primitive PDGFRβ+ CD271+CD73− mesenchymal progenitors, which give rise to proliferative PCs, SMCs, and mesenchymal stem/stromal cells. MB-derived PCs can be further specified to CD274+ capillary and DLK1+ arteriolar PCs with a proinflammatory and contractile phenotype, respectively. SMC maturation was induced using a MEK inhibitor. Establishing the vasculogenic lineage tree, along with identification of stage- and lineage-specific markers, provides a platform for interrogating the molecular mechanisms that regulate vasculogenic cell specification and diversification and manufacturing well-defined mural cell populations for vascular engineering and cellular therapies from hPSCs. Kumar et al. find that mesodermal pericytes and smooth muscle cells in human pluripotent stem cell cultures originate from a common endothelial and mesenchymal cell precursor, the mesenchymoangioblast. They show how different lineages of mural cells are specified from mesenchymoangioblasts and define stage- and lineage-specific markers for vasculogenic cells.
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DOI:
10.1126/science.aad0084
发表时间:
2016-01-08
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Khan JA;Mendelson A;Kunisaki Y;Birbrair A;Kou Y;Arnal-Estapé A;Pinho S;Ciero P;Nakahara F;Ma'ayan A;Bergman A;Merad M;Frenette PS
通讯作者:
Frenette PS
影响因子:
2.5
作者:
Maeda, J;Yamagishi, H;Srivastava, D
通讯作者:
Srivastava, D
影响因子:
6
作者:
Chambers, RC;Leoni, P;Heller, RA
通讯作者:
Heller, RA
影响因子:
10.8
作者:
Bajpai, Vivek K.;Mistriotis, Panagiotis;Andreadis, Stelios T.
通讯作者:
Andreadis, Stelios T.
DOI:
10.1111/j.1749-6632.2009.04967.x
发表时间:
2009-01-01
期刊:
HEMATOPOIETIC STEM CELLS VII
影响因子:
--
作者:
Crisan, Mihaela;Chen, Chien-Wen;Peault, Bruno
通讯作者:
Peault, Bruno