Retinoblastoma protein promotes uterine epithelial cell cycle arrest and necroptosis for embryo invasion

Shun Akaeda, Yasushi Hirota, Yamato Fukui, Shizu Aikawa, Ryoko Shimizu-Hirota, Tetsuaki Kaku, Mona Gebril, Tomoyuki Hirata, Takehiro Hiraoka, Mitsunori Matsuo, Hirofumi Haraguchi, Mayuko Saito-Kanatani, Norihiko Takeda, Tomoyuki Fujii, Yutaka Osuga

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12 Citations (Scopus)


Retinoblastoma protein (RB) encoded by Rb1 is a prominent inducer of cell cycle arrest (CCA). The hormone progesterone (P4) promotes CCA in the uterine epithelium and previous studies indicated that P4 activates RB by reducing the phosphorylated, inactive form of RB. Here, we show that embryo implantation is impaired in uterine-specific Rb1 knockout mice. We observe persistent cell proliferation of the Rb1-deficient uterine epithelium until embryo attachment, loss of epithelial necroptosis, and trophoblast phagocytosis, which correlates with subsequent embryo invasion failure, indicating that Rb1-induced CCA and necroptosis of uterine epithelium are involved in embryo invasion. Pre-implantation P4 supplementation is sufficient to restore these defects and embryo invasion. In Rb1-deficient uterine epithelial cells, TNFα-primed necroptosis is impaired, which is rescued by the treatment with a CCA inducer thymidine or P4 through the upregulation of TNF receptor type 2. TNFα is expressed in the luminal epithelium and the embryo at the embryo attachment site. These results provide evidence that uterine Rb1-induced CCA is involved in TNFα-primed epithelial necroptosis at the implantation site for successful embryo invasion.

Original languageEnglish
Article numbere50927
JournalEMBO Reports
Issue number2
Publication statusPublished - 2021 Feb 3


  • TNFα signaling
  • embryo implantation
  • progesterone
  • trophoblast phagocytosis
  • uterine luminal epithelium

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Genetics


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