Updated on 2025/06/12

写真b

 
MORITA Hitoshi
 
*Items subject to periodic update by Rikkyo University (The rest are reprinted from information registered on researchmap.)
Affiliation*
College of Science Department of Life Science
Title*
Assistant Professor
Degree
PhD ( SOKENDAI )
Campus Career*
  • 4 2022 - Present 
    College of Science   Department of Life Science   Assistant Professor
Profile

To clarify the mechanisms of animal embryonic development, I conduct analyses at the molecular and cellular levels, particularly focusing on cellular dynamics using live imaging techniques on optical microscopes.

 

Research Areas

  • Life Science / Developmental biology

Research History

  • 4 2022 - Present 
    Rikkyo University   College of Science Department of Life Science   Asistant professor

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  • 4 2019 - 3 2022 
    University of Yamanashi   Asistant professor

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  • 10 2016 - 3 2019 
    University of Yamanashi   Assistant professor

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  • 10 2011 - 9 2016 
    Institute of Science and Technology (IST) Austria   Postdoc

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  • 10 2012 - 9 2014 
    Japan Society for the Promotion of Science (JSPS)

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  • 4 2011 - 9 2011 
    National Institute for Basic Biology (NIBB)   Division of Morphogenesis   Postdoc

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Education

  • 4 2006 - 3 2011 
    The Graduate University for Advanced Studies (SOKENDAI)   School of Life Science   Department of Basic Biology

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  • 4 2002 - 3 2006 
    Chiba University   Faculty of Science   Department of Biology

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Papers

  • Studying YAP-Mediated 3D Morphogenesis Using Fish Embryos and Human Spheroids. Peer-reviewed International journal

    Asaoka Y, Morita H, Furumoto H, Heisenberg CP, Furutani-Seiki M

    Methods in Molecular Biology (Clifton, N.J.)1893   167 - 181   2019

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    Language:English   Publishing type:Research paper (scientific journal)  

    The transcription coactivator, Yes-associated protein (YAP), which is a nuclear effector of the Hippo signaling pathway, has been shown to be a mechano-transducer. By using mutant fish and human 3D spheroids, we have recently demonstrated that YAP is also a mechano-effector. YAP functions in three-dimensional (3D) morphogenesis of organ and global body shape by controlling actomyosin-mediated tissue tension. In this chapter, we present a platform that links the findings in fish embryos with human cells. The protocols for analyzing tissue tension-mediated global body shape/organ morphogenesis in vivo and ex vivo using medaka fish embryos and in vitro using human cell spheroids represent useful tools for unraveling the molecular mechanisms by which YAP functions in regulating global body/organ morphogenesis.

    DOI: 10.1007/978-1-4939-8910-2_14

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  • Spatiotemporal expression of the cocaine- and amphetamine-regulated transcript-like (cart-like) gene during zebrafish embryogenesis. Peer-reviewed International journal

    Kawahara A, Morita H, Yanagi K, Suzuki H, Mori T, Ohga R, Taimatsu K

    Gene Expression Patterns : GEP30   1 - 6   8 2018

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    Language:English   Publishing type:Research paper (scientific journal)  

    The cocaine- and amphetamine-regulated transcript (CART) genes are involved in the neural regulation of energy homeostasis; however, their developmental expressions and functions are not fully understood in vertebrates. We have identified a novel zebrafish cart-like gene that encodes a protein of 105 amino acids possessing sequence similarity to zebrafish and mammalian CART proteins. RT-PCR analysis revealed that the cart-like transcripts were maternally supplied and gradually decreased during the cleavage, blastula and gastrula stages; then, transcripts subsequently reaccumulated at the segmentation, pharyngula and hatching stages. Based on a whole-mount in situ hybridization analysis using an antisense cart-like RNA probe, we found that the cart-like transcript was predominantly expressed in both the Rohon-Beard neurons and trigeminal ganglia, suggesting the involvement of the cart-like gene in zebrafish neural development.

    DOI: 10.1016/j.gep.2018.08.002

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  • Developmental expression of the slurp-like1/ly2.3/ly97.3 and slurp-like2/ly2.2/ly97.2 genes during zebrafish early embryogenesis. Peer-reviewed International journal

    Kawahara A, Morita H, Yanagi K, Ishizaka T, Taimatsu K, Ohga R

    Gene Expression Patterns : GEP30   32 - 36   8 2018

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    Language:English   Publishing type:Research paper (scientific journal)  

    Mammalian SLURP1 and SLURP2 belong to the Ly-6/uPAR superfamily and are involved in maintaining the physiological integrity of keratinocytes. However, the developmental expression and functions of other Ly-6/uPAR family genes in vertebrates are still obscure. We have isolated novel Ly-6/uPAR family genes slurp-like1 (ly2.3/ly97.3) and slurp-like2 (ly2.2/ly97.2) in zebrafish. Both the Slurp-like1 and Slurp-like2 proteins contain the typical signal sequence and carboxy-terminal CCXXXXCN (X: an arbitrary amino acid) consensus sequence of the Ly-6/uPAR family but lack a transmembrane domain and a GPI-anchoring signal sequence, suggesting that both proteins may function as secretory proteins. Whole-mount in situ hybridization analysis revealed that slurp-like1 was predominantly expressed in the floor plate of the neural tube and in the hypochord of the notochord at 24 h post-fertilization (hpf) and detected in the liver and intestinal bulb at 72 hpf, while slurp-like2 was expressed in the midbrain and hindbrain at 24 hpf and detected in the liver and pancreas at 72 hpf. Differential expression profiles of the slurp-like1 and slurp-like2 genes suggest the distinct physiological involvement of these genes in zebrafish early embryogenesis.

    DOI: 10.1016/j.gep.2018.08.006

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  • The Physical Basis of Coordinated Tissue Spreading in Zebrafish Gastrulation Peer-reviewed

    Hitoshi Morita, Silvia Grigolon, Martin Bock, S. F. Gabriel Krens, Guillaume Salbreux, Carl-Philipp Heisenberg

    Developmental Cell40 ( 4 ) 354 - 366   2 2017

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.devcel.2017.01.010

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  • Exogenous gene integration mediated by genome editing technologies in zebrafish Peer-reviewed

    Hitoshi Morita, Kiyohito Taimatsu, Kanoko Yanagi, Atsuo Kawahara

    Bioengineered8 ( 3 ) 287 - 295   2017

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    Authorship:Lead author   Language:English  

    DOI: 10.1080/21655979.2017.1300727

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  • YAP is essential for tissue tension to ensure vertebrate 3D body shape Peer-reviewed

    Sean Porazinski, Huijia Wang, Yoichi Asaoka, Martin Behrndt, Tatsuo Miyamoto, Hitoshi Morita, Shoji Hata, Takashi Sasaki, S. F. Gabriel Krens, Yumi Osada, Satoshi Asaka, Akihiro Momoi, Sarah Linton, Joel B. Miesfeld, Brian A. Link, Takeshi Senga, Atahualpa Castillo-Morales, Araxi O. Urrutia, Nobuyoshi Shimizu, Hideaki Nagase, Shinya Matsuura, Stefan Bagby, Hisato Kondoh, Hiroshi Nishina, Carl-Philipp Heisenberg, Makoto Furutani-Seiki

    Nature521 ( 7551 ) 217 - 221   5 2015

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1038/nature14215

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  • Cortical Contractility Triggers a Stochastic Switch to Fast Amoeboid Cell Motility Peer-reviewed

    Verena Ruprecht, Stefan Wieser, Andrew Callan-Jones, Michael Smutny, Hitoshi Morita, Keisuke Sako, Vanessa Barone, Monika Ritsch-Marte, Michael Sixt, Raphael Voituriez, Carl-Philipp Heisenberg

    Cell160 ( 4 ) 673 - 685   2 2015

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.cell.2015.01.008

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  • Molecular and cellular mechanisms of development underlying congenital diseases Peer-reviewed

    Masakazu Hashimoto, Hitoshi Morita, Naoto Ueno

    Congenital Anomalies54 ( 1 ) 1 - 7   2 2014

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    Language:English  

    DOI: 10.1111/cga.12039

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  • Transgenic Xenopus laevis for live imaging in cell and developmental biology Peer-reviewed

    Chiyo Takagi, Kazuhiro Sakamaki, Hitoshi Morita, Yusuke Hara, Makoto Suzuki, Noriyuki Kinoshita, Naoto Ueno

    Development Growth & Differentiation55 ( 4 ) 422 - 433   5 2013

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    Language:English  

    DOI: 10.1111/dgd.12042

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  • Holding On and Letting Go: Cadherin Turnover in Cell Intercalation Peer-reviewed

    Hitoshi Morita, Carl-Philipp Heisenberg

    Developmental Cell24 ( 6 ) 567 - 569   3 2013

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    Authorship:Lead author   Language:English  

    DOI: 10.1016/j.devcel.2013.03.007

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  • Cell movements of the deep layer of non-neural ectoderm underlie complete neural tube closure in Xenopus Peer-reviewed

    Hitoshi Morita, Hiroko Kajiura-Kobayashi, Chiyo Takagi, Takamasa S. Yamamoto, Shigenori Nonaka, Naoto Ueno

    Development139 ( 8 ) 1417 - 1426   4 2012

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1242/dev.073239

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  • Molecular mechanisms of cell shape changes that contribute to vertebrate neural tube closure Peer-reviewed

    Makoto Suzuki, Hitoshi Morita, Naoto Ueno

    Development Growth & Differentiation54 ( 3 ) 266 - 276   4 2012

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  • Nectin-2 and N-cadherin interact through extracellular domains and induce apical accumulation of F-actin in apical constriction of Xenopus neural tube morphogenesis Peer-reviewed

    Hitoshi Morita, Sumeda Nandadasa, Takamasa S. Yamamoto, Chie Terasaka-Iioka, Christopher Wylie, Naoto Ueno

    Development137 ( 8 ) 1315 - 1325   4 2010

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1242/dev.043190

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Misc.

Professional Memberships

  •  
    The Zoological Society of Japan

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    The Molecular Biology Society of Japan

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  •  
    Japanese Society of Developmental Biologists

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Research Projects

  • Analysis of the role of tissue tension in early heart development

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (C) 

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    4 2022 - 3 2023

    Grant number:22K06248

    Grant amount:\4030000 ( Direct Cost: \3100000 、 Indirect Cost:\930000 )

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  • ライブイメージングと定量化による心臓前駆細胞の移動制御機構の解析

    日本学術振興会  科学研究費助成事業 若手研究(B) 

    森田 仁

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    4 2017 - 3 2020

    Authorship:Principal investigator  Grant type:Competitive

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