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RIKEN Center for Developmental Biology

Laboratory for Reconstitutive Developmental Biology

Research Unit Leader: Miki Ebisuya (Ph.D.)
Miki  Ebisuya(Ph.D.)

Our research interests are in cell-cell communications that occur during development of multicellular organisms. The cells communicate with each other to autonomously differentiate into different cell types and to form spatial patterns in a variety of tissues. To understand the mechanisms, we have been reconstituting the cell-cell communications by constructing artificial gene networks in cultured cells.

Research Fields

Physics / Engineering / Biology & Biochemistry / Molecular Biology & Genetics / Multidisciplinary

Research Subjects

  • Reconstitution of cell autonomous differentiation
  • Reconstitution of cell pattern formation

Publications

  1. * Uno M, Honjoh S, Matsuda M, Hoshikawa H, Kishimoto S, Yamamoto T, Ebisuya M, Yamamoto T, Matsumoto K and Nishida E.
    A fasting-responsive signaling pathway that extends life span in C. elegans.
    Cell Rep., 3, 79-91 (2013).
  2. * Tanimura N, Saito M, Ebisuya M, Nishida E and Ishikawa F.
    Stemness-related Factor Sall4 Interacts with Transcription Factors Oct-3/4 and Sox2 and Occupies Oct-Sox Elements in Mouse Embryonic Stem Cells.
    J. Biol. Chem., 288, 5027-5038 (2013).
  3. * Matsuda M, Koga M, Nishida E and Ebisuya M.
    Synthetic Signal Propagation Through Direct Cell-Cell Interaction.
    Sci. Signal., 5, ra31 (2012).
  4. * Matsumura S, Hamasaki M, Yamamoto T, Ebisuya M, Sato M, Nishida E and Toyoshima F.
    ABL1 regulates spindle orientation in adherent cells and mammalian skin.
    Nat. Commun., 3, doi: 10.1038/ncomms1634 (2012).
  5. * Sunadome K, Yamamoto T, Ebisuya M, Kondoh K, Sehara-Fujisawa A and Nishida E.
    ERK5 regulates muscle cell fusion through Klf transcription factors.
    Dev. Cell, 20, 192-205 (2011).
  6. * Mitsushima M, Aoki K, Ebisuya M, Matsumura S, Yamamoto T, Matsuda M, Toyoshima F and Nishida E.
    Revolving movement of a dynamic cluster of actin filaments during mitosis.
    J. Cell Biol., 191, 453-462 (2010).
  7. * Yamazaki T, Fujiwara N, Yukinaga H, Ebisuya M, Shiki T, Kurihara T, Kioka N, Kambe T, Nagao M, Nishida E and Masuda S.
    The closely related RNA helicases, UAP56 and URH49, preferentially form distinct mRNA export machineries and coordinately regulate mitotic progression.
    Mol. Biol. Cell, 21, 2953-2965 (2010).
  8. * Ebisuya M, Yamamoto T, Nakajima M and Nishida E.
    Ripples from neighbouring transcription.
    Nat. Cell Biol., 10, 1106-1113 (2008).
  9. * Yamamoto T*, Ebisuya M* (*Equal first authors), Ashida F, Okamoto K, Yonehara S and Nishida E.
    Continuous ERK activation downregulates antiproliferative genes throughout G1 phase to allow cell-cycle progression.
    Curr. Biol., 16, 1171-1182 (2006).
  10. * Matsubayashi Y, Ebisuya M, Honjoh S and Nishida, E.
    ERK activation propagates in epithelial cell sheets and regulates their migration during wound healing.
    Curr. Biol., 14, 731-735 (2004).

Contact information

2-2-3 Minatojima-minamimachi, Chuo-ku
Kobe, Hyogo
650-0047 Japan

Email: ebisuya [at] cdb.riken.jp

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