The cyclin-dependent kinase inhibitors p27Kip1 and p21Cip1 cooperate to restrict proliferative life span in differentiating ovarian cells

Siwanon Jirawatnotai, David S. Moons, Carlos O. Stocco, Roberta Franks, Dale B. Hales, Geula Gibori, Hiroaki Kiyokawa*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

54 Scopus citations

Abstract

The timing of cellular exit from the cell cycle during differentiation is specific for each cell type or lineage. Granulosa cells in the ovary establish quiescence within several hours after the ovulation-inducing luteinizing hormone surge, whereas they undergo differentiation into corpora lutea. The expression of Cdk inhibitors p21Cip1/Waf1 and p27Kip1 is up-regulated during this process, suggesting that these cell cycle inhibitors are involved in restricting proliferative capacity of differentiating granulosa cells. Here we demonstrate that the lack of p27Kip1 and p21Cip1 synergistically renders granulosa cells extended an proliferative life span. Immunohistochemical analyses demonstrated that corpora lutea of p27Kip1, p21Cip1 double-null mice showed large numbers of cells with bromodeoxyuridine incorporation and high proliferative cell nuclear antigen expression, which were more remarkable than those in p27Kip1 single-deficient mice showing modest hyperproliferation. In contrast, differentiating granulosa cells in p21Cip1-deficient mice ceased proliferation similarly to those in wild-type mice. Interestingly, granulosa cells isolated from p27Kip1, p21Cip1 double-null mice exhibited markedly prolonged proliferative life span in culture, unlike cells with other genotypes. Cultured p27Kip1, p21Cip1 double-null granulosa cells maintained expression of steroidogenic enzymes and gonadotropin receptors through 8-10 passages and could undergo further differentiation in responses to cAMP accumulation. Thus, the cooperation of p27Kip1 and p21Cip1 is critical for withdrawal of granulosa cells from the cell cycle, in concert with luteal differentiation and possibly culture-induced senescence.

Original languageEnglish (US)
Pages (from-to)17021-17027
Number of pages7
JournalJournal of Biological Chemistry
Volume278
Issue number19
DOIs
StatePublished - May 9 2003

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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