2022/11/25 更新

写真b

モリタ ヒトシ
森田 仁
MORITA Hitoshi
*大学が定期的に情報更新している項目(その他は、researchmapの登録情報を転載)
所属*
理学部 生命理学科
職名*
助教
学位
博士(理学) ( 総合研究大学院大学 )
学内職務経歴*
  • 2022年4月 - 現在 
    理学部   生命理学科   助教
 

研究分野

  • ライフサイエンス / 発生生物学

経歴

  • 2022年4月 - 現在 
    立教大学   理学部 生命理学科   助教

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  • 2019年4月 - 2022年3月 
    山梨大学   大学院総合研究部 総合医科学センター 分子生物学   特任助教

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  • 2016年10月 - 2019年3月 
    山梨大学   大学院総合研究部 医学教育センター 発生生物学   特任助教

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  • 2011年10月 - 2016年9月 
    Institute of Science and Technology (IST) Austria   研究員

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  • 2012年10月 - 2014年9月 
    日本学術振興会   海外特別研究員

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  • 2011年4月 - 2011年9月 
    基礎生物学研究所   形態形成研究部門   研究員

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学歴

  • 2006年4月 - 2011年3月 
    総合研究大学院大学   生命科学研究科   基礎生物学専攻

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  • 2002年4月 - 2006年3月 
    千葉大学   理学部   生物学科

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論文

  • Studying YAP-Mediated 3D Morphogenesis Using Fish Embryos and Human Spheroids. 査読有り 国際誌

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

    Methods in molecular biology (Clifton, N.J.)1893   167 - 181   2019年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    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. 査読有り 国際誌

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

    Gene expression patterns : GEP30   1 - 6   2018年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    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. 査読有り 国際誌

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

    Gene expression patterns : GEP30   32 - 36   2018年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1016/j.gep.2018.08.006

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  • The Physical Basis of Coordinated Tissue Spreading in Zebrafish Gastrulation 査読有り

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

    DEVELOPMENTAL CELL40 ( 4 ) 354 - 366   2017年2月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:CELL PRESS  

    Embryo morphogenesis relies on highly coordinated movements of different tissues. However, remarkably little is known about how tissues coordinate their movements to shape the embryo. In zebrafish embryogenesis, coordinated tissue movements first become apparent during "doming," when the blastoderm begins to spread over the yolk sac, a process involving coordinated epithelial surface cell layer expansion and mesenchymal deep cell intercalations. Here, we find that active surface cell expansion represents the key process coordinating tissue movements during doming. By using a combination of theory and experiments, we show that epithelial surface cells not only trigger blastoderm expansion by reducing tissue surface tension, but also drive blastoderm thinning by inducing tissue contraction through radial deep cell intercalations. Thus, coordinated tissue expansion and thinning during doming relies on surface cells simultaneously controlling tissue surface tension and radial tissue contraction.

    DOI: 10.1016/j.devcel.2017.01.010

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  • Exogenous gene integration mediated by genome editing technologies in zebrafish 査読有り

    Hitoshi Morita, Kiyohito Taimatsu, Kanoko Yanagi, Atsuo Kawahara

    BIOENGINEERED8 ( 3 ) 287 - 295   2017年

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    記述言語:英語   出版者・発行元:TAYLOR & FRANCIS INC  

    Genome editing technologies, such as transcription activator-like effector nuclease (TALEN) and the clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated protein (Cas) systems, can induce DNA double-strand breaks (DSBs) at the targeted genomic locus, leading to frameshift-mediated gene disruption in the process of DSB repair. Recently, the technology-induced DSBs followed by DSB repairs are applied to integrate exogenous genes into the targeted genomic locus in various model organisms. In addition to a conventional knock-in technology mediated by homology-directed repair (HDR), novel knock-in technologies using refined donor vectors have also been developed with the genome editing technologies based on other DSB repair mechanisms, including non-homologous end joining (NHEJ) and microhomology-mediated end joining (MMEJ). Therefore, the improved knock-in technologies would contribute to freely modify the genome of model organisms.

    DOI: 10.1080/21655979.2017.1300727

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  • YAP is essential for tissue tension to ensure vertebrate 3D body shape 査読有り

    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 - +   2015年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:NATURE PUBLISHING GROUP  

    Vertebrates have a unique 3D body shape in which correct tissue and organ shape and alignment are essential for function. For example, vision requires the lens to be centred in the eye cup which must in turn be correctly positioned in the head(1). Tissue morphogenesis depends on force generation, force transmission through the tissue, and response of tissues and extracellular matrix to force(2,3). Although a century ago D'Arcy Thompson postulated that terrestrial animal body shapes are conditioned by gravity(4), there has been no animal model directly demonstrating how the aforementioned mechano-morphogenetic processes are coordinated to generate a body shape that withstands gravity. Here we report a unique medaka fish (Oryzias latipes) mutant, hirame (hir), which is sensitive to deformation by gravity. hir embryos display a markedly flattened body caused by mutation of YAP, a nuclear executor of Hippo signalling that regulates organ size. We show that actomyosin-mediated tissue tension is reduced in hir embryos, leading to tissue flattening and tissue misalignment, both of which contribute to body flattening. By analysing YAP function in 3D spheroids of human cells, we identify the Rho GTPase activating protein ARHGAP18 as an effector of YAP in controlling tissue tension. Together, these findings reveal a previously unrecognised function of YAP in regulating tissue shape and alignment required for proper 3D body shape. Understanding this morphogenetic function of YAP could facilitate the use of embryonic stem cells to generate complex organs requiring correct alignment of multiple tissues.

    DOI: 10.1038/nature14215

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  • Cortical Contractility Triggers a Stochastic Switch to Fast Amoeboid Cell Motility 査読有り

    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   2015年2月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:CELL PRESS  

    3D amoeboid cell migration is central to many developmental and disease-related processes such as cancer metastasis. Here, we identify a unique prototypic amoeboid cell migration mode in early zebrafish embryos, termed stable-bleb migration. Stable-bleb cells display an invariant polarized balloon-like shape with exceptional migration speed and persistence. Progenitor cells can be reversibly transformed into stable-bleb cells irrespective of their primary fate and motile characteristics by increasing myosin II activity through biochemical or mechanical stimuli. Using a combination of theory and experiments, we show that, in stable-bleb cells, cortical contractility fluctuations trigger a stochastic switch into amoeboid motility, and a positive feedback between cortical flows and gradients in contractility maintains stable-bleb cell polarization. We further show that rearward cortical flows drive stable-bleb cell migration in various adhesive and non-adhesive environments, unraveling a highly versatile amoeboid migration phenotype.

    DOI: 10.1016/j.cell.2015.01.008

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  • Molecular and cellular mechanisms of development underlying congenital diseases 査読有り

    Masakazu Hashimoto, Hitoshi Morita, Naoto Ueno

    CONGENITAL ANOMALIES54 ( 1 ) 1 - 7   2014年2月

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    記述言語:英語   出版者・発行元:WILEY-BLACKWELL  

    In the last several decades, developmental biology has clarified the molecular mechanisms of embryogenesis and organogenesis. In particular, it has demonstrated that the tool-kit genes essential for regulating developmental processes are not only highly conserved among species, but are also used as systems at various times and places in an organism to control distinct developmental events. Therefore, mutations in many of these tool-kit genes may cause congenital diseases involving morphological abnormalities. This link between genes and abnormal morphological phenotypes underscores the importance of understanding how cells behave and contribute to morphogenesis as a result of gene function. Recent improvements in live imaging and in quantitative analyses of cellular dynamics will advance our understanding of the cellular pathogenesis of congenital diseases associated with aberrant morphologies. In these studies, it is critical to select an appropriate model organism for the particular phenomenon of interest.

    DOI: 10.1111/cga.12039

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  • Transgenic Xenopus laevis for live imaging in cell and developmental biology 査読有り

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

    DEVELOPMENT GROWTH & DIFFERENTIATION55 ( 4 ) 422 - 433   2013年5月

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    記述言語:英語   出版者・発行元:WILEY-BLACKWELL  

    The stable transgenesis of genes encoding functional or spatially localized proteins, fused to fluorescent proteins such as green fluorescent protein (GFP) or red fluorescent protein (RFP), is an extremely important research tool in cell and developmental biology. Transgenic organisms constructed with fluorescent labels for cell membranes, subcellular organelles, and functional proteins have been used to investigate cell cycles, lineages, shapes, and polarity, in live animals and in cells or tissues derived from these animals. Genes of interest have been integrated and maintained in generations of transgenic animals, which have become a valuable resource for the cell and developmental biology communities. Although the use of Xenopus laevis as a transgenic model organism has been hampered by its relatively long reproduction time (compared to Drosophila melanogaster and Caenorhabditis elegans), its large embryonic cells and the ease of manipulation in early embryos have made it a historically valuable preparation that continues to have tremendous research potential. Here, we report on the Xenopus laevis transgenic lines our lab has generated and discuss their potential use in biological imaging.

    DOI: 10.1111/dgd.12042

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  • Holding On and Letting Go: Cadherin Turnover in Cell Intercalation 査読有り

    Hitoshi Morita, Carl-Philipp Heisenberg

    DEVELOPMENTAL CELL24 ( 6 ) 567 - 569   2013年3月

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    記述言語:英語   出版者・発行元:CELL PRESS  

    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 査読有り

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

    DEVELOPMENT139 ( 8 ) 1417 - 1426   2012年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:COMPANY OF BIOLOGISTS LTD  

    In developing vertebrates, the neural tube forms from a sheet of neural ectoderm by complex cell movements and morphogenesis. Convergent extension movements and the apical constriction along with apical-basal elongation of cells in the neural ectoderm are thought to be essential for the neural tube closure (NTC) process. In addition, it is known that non-neural ectoderm also plays a crucial role in this process, as the neural tube fails to close in the absence of this tissue in chick and axolotl. However, the cellular and molecular mechanisms by which it functions in NTC are as yet unclear. We demonstrate here that the non-neural superficial epithelium moves in the direction of tensile forces applied along the dorsal-ventral axis during NTC. We found that this force is partly attributable to the deep layer of non-neural ectoderm cells, which moved collectively towards the dorsal midline along with the superficial layer. Moreover, inhibition of this movement by deleting integrin. 1 function resulted in incomplete NTC. Furthermore, we demonstrated that other proposed mechanisms, such as oriented cell division, cell rearrangement and cell-shape changes have no or only minor roles in the non-neural movement. This study is the first to demonstrate dorsally oriented deep-cell migration in non-neural ectoderm, and suggests that a global reorganization of embryo tissues is involved in NTC.

    DOI: 10.1242/dev.073239

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  • Molecular mechanisms of cell shape changes that contribute to vertebrate neural tube closure 査読有り

    Makoto Suzuki, Hitoshi Morita, Naoto Ueno

    DEVELOPMENT GROWTH & DIFFERENTIATION54 ( 3 ) 266 - 276   2012年4月

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    記述言語:英語   出版者・発行元:WILEY-BLACKWELL  

    During early development of the central nervous system, the neuroepithelial cells undergo dynamic changes in shape, cumulative action of which cause the neural plate to bend mediolaterally to form the neural tube. The apicobasal elongation changes the cuboidal cells into columnar ones, whereas apical constriction minimizes the cell apices, causing them to adopt wedge-like shapes. To achieve the morphological changes required for the formation of a hollow structure, these cellular changes must be controlled in time and space. To date, it is widely accepted that spatial and temporal changes of the cytoskeletal organization are fundamental to epithelial cell shape changes, and that noncetrosomal microtubules assembled along apicobasal axis and actin filaments and non-muscle myosin II at the apical side are central machineries of cell elongation and apical constriction, respectively. Hence, especially in the last decade, intracellular mechanisms regulating these cytoskeletons have been extensively investigated at the molecular level. As a result, several actin-binding proteins, Rho/ROCK pathway, and cellcell adhesion molecules have been proven to be the central regulators of apical constriction, while the regulatory mechanisms of cell elongation remain obscure. In this review, we first describe the distribution and role of cytoskeleton in cell shape changes during neural tube closure, and then summarize the current knowledge about the intracellular proteins that directly modulate the cytoskeletal organization and thus the neural tube closure.

    DOI: 10.1111/j.1440-169X.2012.01346.x

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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 査読有り

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

    DEVELOPMENT137 ( 8 ) 1315 - 1325   2010年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:COMPANY OF BIOLOGISTS LTD  

    Neural tube formation is one of the most dynamic morphogenetic processes of vertebrate development. However, the molecules regulating its initiation are mostly unknown. Here, we demonstrated that nectin-2, an immunoglobulin-like cell adhesion molecule, is involved in the neurulation of Xenopus embryos in cooperation with N-cadherin. First, we found that, at the beginning of neurulation, nectin-2 was strongly expressed in the superficial cells of neuroepithelium. The knockdown of nectin-2 impaired neural fold formation by attenuating F-actin accumulation and apical constriction, a cell-shape change that is required for neural tube folding. Conversely, the overexpression of nectin-2 in non-neural ectoderm induced ectopic apical constrictions with accumulated F-actin. However, experiments with domain-deleted nectin-2 revealed that the intracellular afadin-binding motif, which links nectin-2 and F-actin, was not required for the generation of the ectopic apical constriction. Furthermore, we found that nectin-2 physically interacts with N-cadherin through extracellular domains, and they cooperatively enhanced apical constriction by driving the accumulation of F-actin at the apical cell surface. Interestingly, the accumulation of N-cadherin at the apical surface of neuroepithelium was dependent on the presence of nectin-2, but that of nectin-2 was not affected by depletion of N-cadherin. We propose a novel mechanism of neural tube morphogenesis regulated by the two types of cell adhesion molecules.

    DOI: 10.1242/dev.043190

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MISC

所属学協会

共同研究・競争的資金等の研究

  • 初期心臓形成における組織張力の役割の解析

    日本学術振興会  科学研究費助成事業 基盤研究(C) 

    森田 仁

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    2022年4月 - 2027年3月

    課題番号:22K06248

    配分額:4030000円 ( 直接経費:3100000円 、 間接経費:930000円 )

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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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    2017年4月 - 2020年3月

    担当区分:研究代表者  資金種別:競争的資金

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