Krueppel-like factor 5 is essential for blastocyst development and the normal self-renewal of mouse ESCs.
The transcription factor Klf4 has demonstrated activity in the reprogramming of somatic cells to a pluripotent state, but the molecular mechanism of this process remains unknown. It is, therefore, of great interest to understand the functional role of Klf4 and related genes in ESC regulation. Here, we show that homozygous ... disruption of Klf5 results in the failure of ESC derivation from ICM cells and early embryonic lethality due to an implantation defect. Klf5 KO ESCs show increased expression of several differentiation marker genes and frequent, spontaneous differentiation. Conversely, overexpression of Klf5 in ESCs suppressed the expression of differentiation marker genes and maintained pluripotency in the absence of LIF. Our results also suggest that Klf5 regulates ESC proliferation by promoting phosphorylation of Akt1 via induction of Tcl1. These results, therefore, provide new insights into the functional and mechanistic role of Klf5 in regulation of pluripotency.
Mesh Terms:
Animals, Cell Differentiation, Cell Proliferation, Cells, Cultured, Embryo Implantation, Embryonic Stem Cells, Gene Expression Regulation, Developmental, Homozygote, Kruppel-Like Transcription Factors, Mice, Mice, Knockout, Mutation, Phosphorylation, Proto-Oncogene Proteins, Proto-Oncogene Proteins c-akt, Signal Transduction, Transfection
Animals, Cell Differentiation, Cell Proliferation, Cells, Cultured, Embryo Implantation, Embryonic Stem Cells, Gene Expression Regulation, Developmental, Homozygote, Kruppel-Like Transcription Factors, Mice, Mice, Knockout, Mutation, Phosphorylation, Proto-Oncogene Proteins, Proto-Oncogene Proteins c-akt, Signal Transduction, Transfection
Cell Stem Cell
Date: Nov. 06, 2008
PubMed ID: 18983969
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