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PMID: 12640619 Published · ppublish English Journal Article

Evidence for novel fate of Flk1+ progenitor: contribution to muscle lineage.

Genesis (New York, N.Y. : 2000) ·Vol. 35 ·No. 3 ·2003-03-00 ·Pages 153-9

Motoike T, Markham DW, Rossant J, Sato TN

Abstract

Flk1 is one of the specific cell surface receptors for vascular endothelial growth factor and one of the most specific markers highlighting the earliest stage of hematopoietic and vascular lineages. However, recent new evidence suggests that these Flk1(+) mesodermal progenitor cells also contribute to muscle lineages. All evidence is based on the experiments using in vitro differentiation and in vivo transplantation systems. Although this approach revealed a differentiation potential range of Flk1(+) cells that is wider than previously expected, it fails to determine whether Flk1(+) cells contribute to muscle lineage as part of the normal developmental process. To obtain direct evidence for the fate of Flk1(+) cells in development, we used a knock-in mouse line where Cre is expressed in Flk1(+) cells. Studies with these Cre lines provide direct evidence that Flk1(+) cells are progenitors for muscles, in addition to hematopoietic and vascular endothelial cells.

MeSH Terms
Animals Genes, Reporter Genetic Linkage Integrases/genetics,metabolism Mice Mice, Transgenic Muscle Development/physiology Muscles/embryology,metabolism Receptor, TIE-2/genetics,metabolism Vascular Endothelial Growth Factor Receptor-2/genetics,metabolism Viral Proteins/genetics,metabolism
Chemicals
Viral Proteins Receptor, TIE-2 Vascular Endothelial Growth Factor Receptor-2 Cre recombinase Integrases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Motoike Toshiyuki
The University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390-8573, USA.
Markham David W
Rossant Janet
Sato Thomas N
Article Info
Journal
Genesis (New York, N.Y. : 2000)
Abbr.
Genesis
ISSN
1526-954X
Published
2003-03-00
Pages
153-9
Language
English
Region
United States
NLM ID
100931242
Subset
IM
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