Trophoblast cell lineage in cloned mouse embryos

Mayumi Oda, Kunio Shiota, Satoshi Tanaka

研究成果: Review article査読

13 被引用数 (Scopus)

抄録

Most conceptuses derived by somatic cell nuclear transfer (SCNT) in mice undergo developmental arrest as a result of embryonic or extraembryonic defects. Even when fetuses survive to term, prominent placental overgrowth or placentomegaly is often present, indicating that SCNT affects the development of trophoblast cell lineage. The trophoblast cell lineage is established at the blastocyst stage when the stem cell population of the trophoblast cell lineage resides in the polar trophectoderm. Therefore, it is possible that the developmental arrest and placentomegaly that accompany SCNT are induced by insufficient reprogramming of the donor somatic nucleus to enable the cells to acquire full potency as stem cells of the trophoblast cell lineage. Despite the abnormalities of the extraembryonic tissues of SCNT embryos, trophoblast stem (TS) cell lines have been successfully isolated from SCNT blastocysts and their properties appear to be indistinguishable from those of TS cells derived from native blastocysts. This suggests that SCNT does not affect the emergence and autonomous properties of TS cells. In this review, we discuss specification of cell lineage and the extent of reprogramming of TS cells in SCNT blastocysts.

本文言語English
ページ(範囲)285-291
ページ数7
ジャーナルDevelopment Growth and Differentiation
52
3
DOI
出版ステータスPublished - 2010 4
外部発表はい

ASJC Scopus subject areas

  • Developmental Biology
  • Cell Biology

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