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Kensuke Futai PhD

TitleAssociate Professor
InstitutionUMass Chan Medical School
DepartmentNeurobiology
AddressUMass Chan Medical School
366 Plantation Street, NERB
Worcester MA 01605
Phone774-455-4318
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    Other Positions
    InstitutionT.H. Chan School of Medicine
    DepartmentBrudnick Neuropsychiatric Research Institute

    InstitutionT.H. Chan School of Medicine
    DepartmentNeurobiology

    InstitutionT.H. Chan School of Medicine
    DepartmentNeuroNexus Institute

    InstitutionT.H. Chan School of Medicine
    DepartmentPsychiatry

    InstitutionMorningside Graduate School of Biomedical Sciences
    DepartmentInterdisciplinary Graduate Program

    InstitutionMorningside Graduate School of Biomedical Sciences
    DepartmentMD/PhD Program

    InstitutionMorningside Graduate School of Biomedical Sciences
    DepartmentNeuroscience

    InstitutionUMass Chan Programs, Centers and Institutes
    DepartmentBrudnick Neuropsychiatric Research Institute


    Collapse Biography 
    Collapse education and training
    Kyushu University, Fukuoka, , JapanBSBiology
    Kyushu University, Fukuoka, , JapanMSBiology
    University of Tokyo, Tokyo, , JapanPHDNeurophysiology
    Collapse awards and honors
    2012 - 2015Whitehall Foundation

    Collapse Overview 
    Collapse overview
    Kensuke Futai, Ph.D.

    The roles of Inhibitory neurons in neuropsychiatric diseases

    Our research is focused on investigating the relationship between the dysregulation of synaptic function and neuropsychiatric diseases such as schizophrenia and autism spectrum disorders (ASD) by exploring the regulatory mechanism of inhibitory neurons-mediated synaptic transmission. Synapses are a specialized junction of cell-cell contacts that allow for communication between neurons. Synaptic transmission is mediated by neurotransmitters that are released from a presynaptic terminal and act on corresponding receptors on the postsynaptic dendrite. In the mammalian central nervous system, the most excitatory neurons use glutamate as a neurotransmitter while inhibitory neurons use GABA. Neuronal signal processing is mediated by the integration of both excitatory and inhibitory synaptic responses. Therefore, precise regulatory mechanisms must exist to maintain the balance of excitatory and inhibitory synaptic transmission “E/I balance”. It is becoming increasingly clear that neuropsychiatric diseases may arise from the dysregulation of inhibitory neuronal function which leads to a change in the E/I balance. This would suggest that the restoration of inhibitory function can be a possible direction for therapeutic direction.

    How can we restore inhibitory function? To answer this question, we must understand how inhibitory neurons are activated by excitatory inputs and how the disease-related molecules dysregulate synaptic function. Unfortunately, not much is known about these important topics. Most of our knowledge on excitatory transmission for example is based on studies between two synaptically connected excitatory neurons, but our understanding of excitatory synapses on inhibitory neurons is limited.

    The first research aim for my laboratory is the characterization of excitatory synaptic transmission on inhibitory neurons. The second research aim is to investigate the roles of autism-related genes, such as neuroligin, neurexin, and Shank in excitatory and inhibitory synaptic transmission. We will use a multidisciplinary approach, building on our experiences in electrophysiology and molecular biology techniques to study the role of inhibitory neurons and disease-related molecules with respect to the E-I balance in the hippocampus and cortex.


    Collapse Rotation Projects

    Rotation Projects

    The Futai laboratory seeks highly motivated graduate students who have interest in the roles of risk genes of neuropsychiatric diseases, such as autism and schizophrenia, on neuronal function.Rotation students will typically work side-by-side with Kenny Futai or Postdoctoral Fellows, and give one laboratory meeting presentation at the conclusion of their rotation project.

    Rotation projects

    1. The roles of the risk genes of neuropsychiatric diseases on neuronal structure and synaptic function
    2. The roles of the scaffold molecules in synapse maturation, synaptic transmission and synaptic plasticity
    3. Characterization of gultamate receptors which express in interneruon

    Collapse Post Docs

    Postdoctoral Position Available

    A postdoctoral position is available to study in this laboratory. Contact Kensuke Futai for additional details.



    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Tzeng TC, Hasegawa Y, Iguchi R, Cheung A, Caffrey DR, Thatcher EJ, Mao W, Germain G, Tamburro ND, Okabe S, Heneka MT, Latz E, Futai K, Golenbock DT. Inflammasome-derived cytokine IL18 suppresses amyloid-induced seizures in Alzheimer-prone mice. Proc Natl Acad Sci U S A. 2018 09 04; 115(36):9002-9007. PMID: 30127003.
      Citations: 26     Fields:    Translation:AnimalsCells
    2. Tsantoulas C, Denk F, Signore M, Nassar MA, Futai K, McMahon SB. Mice lacking Kcns1 in peripheral neurons show increased basal and neuropathic pain sensitivity. Pain. 2018 Aug; 159(8):1641-1651. PMID: 29697531.
      Citations: 11     Fields:    Translation:AnimalsCells
    3. Mao W, Salzberg AC, Uchigashima M, Hasegawa Y, Hock H, Watanabe M, Akbarian S, Kawasawa YI, Futai K. Activity-Induced Regulation of Synaptic Strength through the Chromatin Reader L3mbtl1. Cell Rep. 2018 06 12; 23(11):3209-3222. PMID: 29898393.
      Citations: 14     Fields:    Translation:AnimalsCells
    4. Hasegawa Y, Mao W, Saha S, Gunner G, Kolpakova J, Martin GE, Futai K. Luciferase shRNA Presents off-Target Effects on Voltage-Gated Ion Channels in Mouse Hippocampal Pyramidal Neurons. eNeuro. 2017 Sep-Oct; 4(5). PMID: 29034317.
      Citations: 8     Fields:    Translation:AnimalsCells
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