Updated on 2026/08/25

写真a

 
LIU XINYI
 
Organization
Brain Research Institute Field for Brain Function and Repair Dept. of System Pathology for Neurological Disorders Assistant Professor
Title
Assistant Professor
Contact information
メールアドレス
External link

Degree

  • 博士(医学) ( 2017.3   神戸大学 )

Research Interests

  • transcranial imaging

  • in vivo brain imaging

  • skull clearing

  • two-photon microscopy

  • longitudinal imaging

Research Areas

  • Life Science / Basic brain sciences

Research History (researchmap)

  • 新潟大学脳研究所   システム脳病態学分野   助教

    2023.4

      More details

  • 新潟大学脳研究所   システム脳病態学分野   学術振興会外国人特別研究員

    2021.4 - 2023.3

      More details

  • 新潟大学脳研究所   システム脳病態学分野   機関研究員

    2019.9 - 2021.3

      More details

  • 新潟大学大学院医歯学総合研究科   薬理学分野   特任助教

    2019.4 - 2019.8

      More details

  • 神戸大学大学院医学研究科   血管生物学分野   教育研究補佐員

    2017.4 - 2019.3

      More details

Research History

  • Niigata University   Dept. of System Pathology for Neurological Disorders, Field for Brain Function and Repair, Brain Research Institute   Assistant Professor

    2026.4

  • Niigata University   Brain Research Institute   Assistant Professor

    2023.4 - 2026.3

  • Niigata University   Graduate School of Medical and Dental Sciences   Specially Appointed Assistant Professor

    2019.4 - 2019.9

Education

  • 神戸大学大学院医学研究科   医科学専攻 博士課程

    2011.10 - 2017.3

      More details

 

Papers

  • Single-cell synaptome mapping of endogenous protein subpopulations in mammalian brain Reviewed

    Motokazu Uchigashima, Risa Iguchi, Kazuma Fujii, Kaito Shiku, Pratik Kumar, Xinyi Liu, Mari Isogai, Chiaki Hoshino, Manabu Abe, Motohiro Nozumi, Yosuke Okamura, Michihiro Igarashi, Kenji Sakimura, Ryoma Bise, Luke D. Lavis, Takayasu Mikuni

    Nature Communications   16 ( 1 )   2025.11

     More details

    Language:English   Publishing type:Research paper (scientific journal)   Publisher:Springer Science and Business Media LLC  

    DOI: 10.1038/s41467-025-65813-w

    researchmap

    Other Link: https://www.nature.com/articles/s41467-025-65813-w

  • SeeThrough: a rationally designed skull clearing technique for in vivo brain imaging Reviewed International coauthorship

    Xinyi Liu, Motokazu Uchigashima, Ikumi Oomoto, Yoshihito Saito, Hitoshi Uchida, Shinya Oginezawa, Keiko Masuda, Daisuke Satoh, Manabu Abe, Kenji Sakimura, Yoshihiro Shimizu, Masanori Murayama, Kazuki Tainaka, Takayasu Mikuni

    Nature Communications   16 ( 1 )   2025.8

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:Springer Science and Business Media LLC  

    DOI: 10.1038/s41467-025-62836-1

    researchmap

    Other Link: https://www.nature.com/articles/s41467-025-62836-1

  • Blood and lymphatic systems are segregated by the FLCN tumor suppressor. Reviewed International journal

    Ikue Tai-Nagara, Yukiko Hasumi, Dai Kusumoto, Hisashi Hasumi, Keisuke Okabe, Tomofumi Ando, Fumio Matsuzaki, Fumiko Itoh, Hideyuki Saya, Chang Liu, Wenling Li, Yoh-Suke Mukouyama, W Marston Linehan, Xinyi Liu, Masanori Hirashima, Yutaka Suzuki, Shintaro Funasaki, Yorifumi Satou, Mitsuko Furuya, Masaya Baba, Yoshiaki Kubota

    Nature communications   11 ( 1 )   6314 - 6314   2020.12

     More details

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

    Blood and lymphatic vessels structurally bear a strong resemblance but never share a lumen, thus maintaining their distinct functions. Although lymphatic vessels initially arise from embryonic veins, the molecular mechanism that maintains separation of these two systems has not been elucidated. Here, we show that genetic deficiency of Folliculin, a tumor suppressor, leads to misconnection of blood and lymphatic vessels in mice and humans. Absence of Folliculin results in the appearance of lymphatic-biased venous endothelial cells caused by ectopic expression of Prox1, a master transcription factor for lymphatic specification. Mechanistically, this phenotype is ascribed to nuclear translocation of the basic helix-loop-helix transcription factor Transcription Factor E3 (TFE3), binding to a regulatory element of Prox1, thereby enhancing its venous expression. Overall, these data demonstrate that Folliculin acts as a gatekeeper that maintains separation of blood and lymphatic vessels by limiting the plasticity of committed endothelial cells.

    DOI: 10.1038/s41467-020-20156-6

    PubMed

    researchmap

  • Semaphorin 3G Provides a Repulsive Guidance Cue to Lymphatic Endothelial Cells via Neuropilin-2/PlexinD1. Reviewed International journal

    Xinyi Liu, Akiyoshi Uemura, Yoko Fukushima, Yutaka Yoshida, Masanori Hirashima

    Cell reports   17 ( 9 )   2299 - 2311   2016.11

     More details

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

    The vertebrate circulatory system is composed of closely related blood and lymphatic vessels. It has been shown that lymphatic vascular patterning is regulated by blood vessels during development, but its molecular mechanisms have not been fully elucidated. Here, we show that the artery-derived ligand semaphorin 3G (Sema3G) and the endothelial cell receptor PlexinD1 play a role in lymphatic vascular patterning. In mouse embryonic back skin, genetic inactivation of Sema3G or PlexinD1 results in abnormal artery-lymph alignment and reduced lymphatic vascular branching. Conditional ablation in mice demonstrates that PlexinD1 is primarily required in lymphatic endothelial cells (LECs). In vitro analyses show that Sema3G binds to neuropilin-2 (Nrp2), which forms a receptor complex with PlexinD1. Sema3G induces cell collapse in an Nrp2/PlexinD1-dependent manner. Our findings shed light on a molecular mechanism by which LECs are distributed away from arteries and form a branching network during lymphatic vascular development.

    DOI: 10.1016/j.celrep.2016.11.008

    PubMed

    researchmap

Research Projects

  • A Novel Techniques for In Vivo Neuronal Imaging in the Mouse Brain

    Grant number:25K18949

    2025.4 - 2027.3

    System name:Grants-in-Aid for Scientific Research

    Research category:Grant-in-Aid for Early-Career Scientists

    Awarding organization:Japan Society for the Promotion of Science

      More details

    Authorship:Principal investigator 

    Grant amount:\4810000 ( Direct Cost: \3700000 、 Indirect Cost:\1110000 )

    researchmap

  • Imaging functional synaptic plasticity during motor learning

    Grant number:21F21113

    2021.4 - 2023.3

    System name:Grants-in-Aid for Scientific Research

    Research category:Grant-in-Aid for JSPS Fellows

    Awarding organization:Japan Society for the Promotion of Science

      More details

    Grant amount:\2300000 ( Direct Cost: \2300000 )

    researchmap

  • Platelet activation plays a repulsive role of lymphatic to blood vessels in mouse peripheral tissues

    Grant number:18K15005

    2018.4 - 2020.3

    System name:Grants-in-Aid for Scientific Research

    Research category:Grant-in-Aid for Early-Career Scientists

    Awarding organization:Japan Society for the Promotion of Science

    Liu Xinyi

      More details

    Authorship:Principal investigator 

    Grant amount:\4160000 ( Direct Cost: \3200000 、 Indirect Cost:\960000 )

    Lymphatic vessels are established as a vasculature separate from blood vessels in peripheral tissues.In this study, we analyzed Phospholipase Cγ2 (Plcg2) knockout mice, which lack platelet activation and show blood-filled lymphatic vasculature. We detected lymph-blood misconnections in embryonic back skin of Plcg2 knockout mice by fluorescent angiography, indicating the role of platelets in the maintenance of lymph-blood partitioning during lymphatic vessel elongation. We also performed time-lapse analysis and found a retraction of LEC protrusion in vitro. These effects were inhibited by an inhibitor of TGF-β signals, while TGF-β induced a retraction of LEC protrusion. In vivo analysis indicates the role of TGF-β in keeping lymphatic vessels separate from blood vessels. These results indicate a novel role for platelets in partitioning blood and lymphatic vascular compartments by promoting LEC retraction in mouse peripheral tissues.

    researchmap

  • A novel screen for mouse models of embryonic disease

    Grant number:17K19526

    2017.6 - 2019.3

    System name:Grants-in-Aid for Scientific Research

    Research category:Grant-in-Aid for Challenging Research (Exploratory)

    Awarding organization:Japan Society for the Promotion of Science

    HIRASHIMA MASANORI, LIU Xinyi, UETA Koji, OGASAWARA Rina

      More details

    Grant amount:\6500000 ( Direct Cost: \5000000 、 Indirect Cost:\1500000 )

    In this study, we tried to establish an efficient screen for mouse models of embryonic disease. This screening strategy has an advantage in that it does not require breeding of mice that do not show the embryonic phenotype of interest. By using this screen, we searched for novel mouse models and gene mutations causing embryonic edema. Embryonic edema is detected as increased nuchal translucency by ultrasonography in 1% of human pregnancy cases. We have so far investigated more than one thousand mutant mouse embryos. We found 21 and 4 embryos showing edema and eye loss, respectively. This study will contribute in future to the development of early diagnosis using biomarkers and of effective drugs in mouse models.

    researchmap