| Literature DB >> 25640817 |
Koji Hayakawa1, Emi Himeno1, Satoshi Tanaka1, Tilo Kunath2.
Abstract
The isolation of stable trophoblast stem (TS) cell lines from early mouse embryos has provided a useful cell culture model to study trophoblast development. TS cells are derived from pre-implantation blastocysts or from the extraembryonic ectoderm of early post-implantation embryos. The derivation and maintenance of mouse TS cells is dependent upon continuous fibroblast growth factor (FGF) signaling. Gene expression analysis, differentiation in culture, and chimera formation show that TS cells accurately model the mouse trophoblast lineage. This unit describes how to derive, maintain, and manipulate TS cells, including DNA transfection and chimera formation.Entities:
Keywords: FGF4; TS cells; extraembryonic ectoderm; trophectoderm; trophoblast; trophoblast stem cells
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Year: 2015 PMID: 25640817 DOI: 10.1002/9780470151808.sc01e04s32
Source DB: PubMed Journal: Curr Protoc Stem Cell Biol ISSN: 1938-8969