この論文にアクセスする

抄録

肝細胞の分裂に必須の時計遺伝子 --新しい分子機能を解明、肝疾患の予防や治療にも期待--. 京都大学プレスリリース. 2017-12-25.

Liver metabolism undergoes robust circadian oscillations in gene expression and enzymatic activity essential for liver homeostasis, but whether the circadian clock controls homeostatic self-renewal of hepatocytes is unknown. Here we show that hepatocyte polyploidization is markedly accelerated around the central vein, the site of permanent cell self-renewal, in mice deficient in circadian Period genes. In these mice, a massive accumulation of hyperpolyploid mononuclear and binuclear hepatocytes occurs due to impaired mitogen-activated protein kinase phosphatase 1 (Mkp1)-mediated circadian modulation of the extracellular signal-regulated kinase (Erk1/2) activity. Time-lapse imaging of hepatocytes suggests that the reduced activity of Erk1/2 in the midbody during cytokinesis results in abscission failure, leading to polyploidization. Manipulation of Mkp1 phosphatase activity is sufficient to change the ploidy level of hepatocytes. These data provide clear evidence that the Period genes not only orchestrate dynamic changes in metabolic activity, but also regulate homeostatic self-renewal of hepatocytes through Mkp1-Erk1/2 signaling pathway.

収録刊行物

  • Nature Communications

    Nature Communications (8), 2017-12-21

    Springer Nature

キーワード

各種コード

  • NII論文ID(NAID)
    120006373904
  • 本文言語コード
    ENG
  • 資料種別
    journal article
  • ISSN
    2041-1723
  • データ提供元
    IR 
ページトップへ