Skp2 contributes to cell cycle progression in trophoblast stem cells and to placental development

Yuhei Yamauchi, Akihiro Nita, Masaaki Nishiyama, Yoshiharu Muto, Hideyuki Shimizu, Hirokazu Nakatsumi, Keiichi I. Nakayama

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

All trophoblast subtypes of the placenta are derived from trophoblast stem cells (TSCs). TSCs have the capacity to self-renew, but how the proliferation of these cells is regulated in the undifferentiated state has been largely unclear. We now show that the F-box protein Skp2 regulates the proliferation of TSCs and thereby plays a pivotal role in placental development in mice on the C57BL/6 background. The placenta of Skp2−/− mouse embryos on the C57BL/6 background was smaller than that of their Skp2+/+ littermates, with the mutant embryos also manifesting intrauterine growth retardation. Although the Skp2−/− mice were born alive, most of them died before postnatal day 21, presumably as a result of placental defects. Depletion of Skp2 in TSCs cultured in the undifferentiated state resulted in a reduced rate of proliferation and arrest of the cell cycle in G1 phase, indicative of a defect in self-renewal capacity. The cell cycle arrest apparent in Skp2-deficient TSCs was reversed by additional ablation of the cyclin-dependent kinase inhibitor (CKI) p57 but not by that of the CKI p27. Our results thus suggest that Skp2-mediated degradation of p57 is an important determinant of the self-renewal capacity of TSCs during placental development, at least in mice of certain genetic backgrounds.

Original languageEnglish
Pages (from-to)427-438
Number of pages12
JournalGenes to Cells
Volume25
Issue number6
DOIs
Publication statusPublished - Jun 1 2020
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Genetics
  • Cell Biology

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