Neuroepithelial cells supply an initial transient wave of MSC differentiation

被引:404
作者
Takashima, Yasuhiro
Era, Takumi
Nakao, Kazuki
Kondo, Saki
Kasuga, Masato
Smith, Austin G.
Nishikawa, Shin-Ichi
机构
[1] Riken Ctr Dev Biol, Lab Stem Cell Biol, Chuo Ku, Kobe, Hyogo 6500047, Japan
[2] Riken Ctr Dev Biol, Lab Anim Resources & Genet Engn, Chuo Ku, Kobe, Hyogo 6500047, Japan
[3] Kobe Univ, Grad Sch Med, Div Diabet & Digest & Kidney Dis, Dept Clin Mol Med,Chuo Ku, Kobe, Hyogo 6500017, Japan
[4] Univ Tokyo, Inst Med Sci, Mol Genet Lab, Tokyo 1088639, Japan
[5] Univ Cambridge, Inst Stem Cell Biol, Cambridge CB2 1QT, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.cell.2007.04.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mesenchymal stem cells (MSCs) are defined as cells that undergo sustained in vitro growth and are able to give rise to multiple mesenchymal lineages. Although MSCs are already used in regenerative medicine little is known about their in vivo behavior and developmental derivation. Here, we show that the earliest wave of MSC in the embryonic trunk is generated from Sox1(+) neuroepithelium but not from mesoderm. Using lineage marking by direct gfp knock- in and Cre-recombinase mediated lineage tracing, we provide evidence that Sox1(+) neuroepithelium gives rise to MSCs in part through a neural crest intermediate stage. This pathway can be distinguished from the pathway through which Sox1(+) cells give rise to oligodendrocytes by expression of PDGFR beta and A2B5. MSC recruitment from this pathway, however, is transient and is replaced by MSCs from unknown sources. We conclude that MSC can be defined as a definite in vivo entity recruited from multiple developmental origins.
引用
收藏
页码:1377 / 1388
页数:12
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