Kensuke Futai PhD
Title Assistant Professor
Institution University of Massachusetts Medical School
Department Psychiatry
Address University of Massachusetts Medical School
303 Belmont Street
Worcester MA 01605
Email
Other Positions
Institution UMMS - Graduate School of Biomedical Sciences
Department Interdisciplinary Graduate Program

Institution UMMS - Graduate School of Biomedical Sciences
Department Neuroscience

Institution UMMS - Programs, Centers and Institutes
Department Brudnick Neuropsychiatric Research Institute
Awards and Honors
2012 Whitehall Foundation
Narrative
 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.

Publications
1. Futai K, Doty CD, Baek B, Ryu J, Sheng M. Specific trans-synaptic interaction with inhibitory interneuronal neurexin underlies differential ability of neuroligins to induce functional inhibitory synapses. J Neurosci. 2013 Feb 20; 33(8):3612-23.
  View in: PubMed
 
2. Almeida S, Zhang Z, Coppola G, Mao W, Futai K, Karydas A, Geschwind MD, Tartaglia MC, Gao F, Gianni D, Sena-Esteves M, Geschwind DH, Miller BL, Farese RV, Gao FB. Induced Pluripotent Stem Cell Models of Progranulin-Deficient Frontotemporal Dementia Uncover Specific Reversible Neuronal Defects. Cell Rep. 2012 Oct 9.
  View in: PubMed
 
3. Hayashi Y, Okamoto K, Bosch M, Futai K. Roles of neuronal activity-induced gene products in hebbian and homeostatic synaptic plasticity, tagging, and capture. Adv Exp Med Biol. 2012; 970:335-54.
  View in: PubMed
 
4. Carlén M, Meletis K, Siegle JH, Cardin JA, Futai K, Vierling-Claassen D, Rühlmann C, Jones SR, Deisseroth K, Sheng M, Moore CI, Tsai LH. A critical role for NMDA receptors in parvalbumin interneurons for gamma rhythm induction and behavior. Mol Psychiatry. 2012 May; 17(5):537-48.
  View in: PubMed
 
5. Jo J, Son GH, Winters BL, Kim MJ, Whitcomb DJ, Dickinson BA, Lee YB, Futai K, Amici M, Sheng M, Collingridge GL, Cho K. Muscarinic receptors induce LTD of NMDAR EPSCs via a mechanism involving hippocalcin, AP2 and PSD-95. Nat Neurosci. 2010 Oct; 13(10):1216-24.
  View in: PubMed
 
6. Hoogenraad CC, Popa I, Futai K, Martinez-Sanchez E, Sanchez-Martinez E, Wulf PS, van Vlijmen T, Dortland BR, Oorschot V, Govers R, Monti M, Heck AJ, Sheng M, Klumperman J, Rehmann H, Jaarsma D, Kapitein LC, van der Sluijs P. Neuron specific Rab4 effector GRASP-1 coordinates membrane specialization and maturation of recycling endosomes. PLoS Biol. 2010 Jan; 8(1):e1000283.
  View in: PubMed
 
7. Ryu J, Futai K, Feliu M, Weinberg R, Sheng M. Constitutively active Rap2 transgenic mice display fewer dendritic spines, reduced extracellular signal-regulated kinase signaling, enhanced long-term depression, and impaired spatial learning and fear extinction. J Neurosci. 2008 Aug 13; 28(33):8178-88.
  View in: PubMed
 
8. Ochiishi T, Futai K, Okamoto K, Kameyama K, Kosik KS. Regulation of AMPA receptor trafficking by delta-catenin. Mol Cell Neurosci. 2008 Dec; 39(4):499-507.
  View in: PubMed
 
9. Hung AY, Futai K, Sala C, Valtschanoff JG, Ryu J, Woodworth MA, Kidd FL, Sung CC, Miyakawa T, Bear MF, Weinberg RJ, Sheng M. Smaller dendritic spines, weaker synaptic transmission, but enhanced spatial learning in mice lacking Shank1. J Neurosci. 2008 Feb 13; 28(7):1697-708.
  View in: PubMed
 
10. Kim MJ, Futai K, Jo J, Hayashi Y, Cho K, Sheng M. Synaptic accumulation of PSD-95 and synaptic function regulated by phosphorylation of serine-295 of PSD-95. Neuron. 2007 Nov 8; 56(3):488-502.
  View in: PubMed
 
11. Futai K, Kim MJ, Hashikawa T, Scheiffele P, Sheng M, Hayashi Y. Retrograde modulation of presynaptic release probability through signaling mediated by PSD-95-neuroligin. Nat Neurosci. 2007 Feb; 10(2):186-95.
  View in: PubMed
 
12. Futai K. [Hellow, PSJ]. Nippon Seirigaku Zasshi. 2005; 67(5):183-4.
  View in: PubMed
 
13. Nakagawa T, Futai K, Lashuel HA, Lo I, Okamoto K, Walz T, Hayashi Y, Sheng M. Quaternary structure, protein dynamics, and synaptic function of SAP97 controlled by L27 domain interactions. Neuron. 2004 Oct 28; 44(3):453-67.
  View in: PubMed
 
14. Sala C, Futai K, Yamamoto K, Worley PF, Hayashi Y, Sheng M. Inhibition of dendritic spine morphogenesis and synaptic transmission by activity-inducible protein Homer1a. J Neurosci. 2003 Jul 16; 23(15):6327-37.
  View in: PubMed
 
15. Futai K, Okada M, Matsuyama K, Takahashi T. High-fidelity transmission acquired via a developmental decrease in NMDA receptor expression at an auditory synapse. J Neurosci. 2001 May 15; 21(10):3342-9.
  View in: PubMed
 
16. Ito I, Futai K, Katagiri H, Watanabe M, Sakimura K, Mishina M, Sugiyama H. Synapse-selective impairment of NMDA receptor functions in mice lacking NMDA receptor epsilon 1 or epsilon 2 subunit. J Physiol. 1997 Apr 15; 500 ( Pt 2):401-8.
  View in: PubMed
 
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Co-Authors  
Gao, Fen-Biao
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Physical Neighbors  
Breslin, Daniel
Cavallero, Linda
Kolodziej, Monika
Thompson, Rachel
Merritt, Virginia

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