2025/09/01 更新

写真a

オカモト カズキ
岡本 和樹
OKAMOTO Kazuki
所属
脳研究所 基礎神経科学部門 細胞病態学 講師
職名
講師
外部リンク

学位

  • 博士(薬科学) ( 2019年3月   東京大学 )

  • 修士(薬科学) ( 2016年3月   東京大学 )

  • 学士(薬科学) ( 2014年3月   東京大学 )

研究分野

  • ライフサイエンス / 神経形態学

経歴(researchmap)

  • 新潟大学   脳研究所 基礎神経科学部門 細胞病態学分野   講師

    2025年4月 - 現在

      詳細を見る

  • 国立研究開発法人科学技術振興機構   戦略的創造研究推進事業(さきがけ)   さきがけ研究員(兼任)

    2023年10月 - 現在

      詳細を見る

  • 順天堂大学 大学院医学研究科   脳回路形態学   助教

    2021年11月 - 2025年3月

      詳細を見る

    国名:日本国

    researchmap

  • 順天堂大学   医学部 神経生物学・形態学講座   特任助教

    2021年4月 - 2021年10月

      詳細を見る

  • 順天堂大学   医学部 神経生物学・形態学講座   特別研究員PD

    2019年4月 - 2021年3月

      詳細を見る

  • 東京大学   大学院薬学系研究科 薬品作用学教室   特別研究員DC1

    2016年4月 - 2019年3月

      詳細を見る

▶ 全件表示

経歴

  • 新潟大学   脳研究所 基礎神経科学部門 細胞病態学   講師

    2025年4月 - 現在

所属学協会

 

論文

  • Sleep homeostasis in lizards and the role of the cortex. 国際誌

    Sena Hatori, Sho T Yamaguchi, Riho Kobayashi, Kazuki Okamoto, Zhiwen Zhou, Koki T Kotake, Futaba Matsui, Hiroyuki Hioki, Hiroaki Norimoto

    Proceedings of the National Academy of Sciences of the United States of America   122 ( 16 )   e2415929122   2025年4月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Slow-wave sleep (SWS) and rapid eye movement sleep are the two primary components of electrophysiological sleep (e-sleep) in mammals and birds. Slow waves in the cortex not only characterize SWS but are also used as biological markers for sleep homeostasis, given their rebound after sleep deprivation (SD). Recently, it has been reported that the Australian dragon Pogona vitticeps exhibits a two-stage sleep pattern in the dorsal ventricular ridge (DVR), which includes a homologue of the mammalian claustrum (CLA). It remains unclear whether reptilian e-sleep, which has been characterized by activity outside the cortex, compensates for sleep loss, as observed in mammals. We here report a significant rebound in the local field potential (LFP) after 7 h of SD. Meanwhile, the mean bout length of each sleep state remained unaffected. We further investigated a possible role of the cortex in e-sleep regulation and homeostasis in Pogona and found that although a corticotomy had no obvious effect on the LFP features of baseline sleep, it abolished LFP power rebound in the CLA/DVR after SD. These findings suggest that e-sleep homeostasis is a common feature in amniotes and that the cortex is involved in regulating activity rebounds in reptiles and mammals.

    DOI: 10.1073/pnas.2415929122

    PubMed

    researchmap

  • A method to analyze gene expression profiles from hippocampal neurons electrophysiologically recorded in vivo

    Haruya Yagishita, Yasuhiro Go, Kazuki Okamoto, Nariko Arimura, Yuji Ikegaya, Takuya Sasaki

    Frontiers in Neuroscience   18   2024年4月

     詳細を見る

    掲載種別:研究論文(学術雑誌)   出版者・発行元:Frontiers Media SA  

    Hippocampal pyramidal neurons exhibit diverse spike patterns and gene expression profiles. However, their relationships with single neurons are not fully understood. In this study, we designed an electrophysiology-based experimental procedure to identify gene expression profiles using RNA sequencing of single hippocampal pyramidal neurons whose spike patterns were recorded in living mice. This technique involves a sequence of experiments consisting of in vivo juxtacellular recording and labeling, brain slicing, cell collection, and transcriptome analysis. We demonstrated that the expression levels of a subset of genes in individual hippocampal pyramidal neurons were significantly correlated with their spike burstiness, submillisecond-level spike rise times or spike rates, directly measured by in vivo electrophysiological recordings. Because this methodological approach can be applied across a wide range of brain regions, it is expected to contribute to studies on various neuronal heterogeneities to understand how physiological spike patterns are associated with gene expression profiles.

    DOI: 10.3389/fnins.2024.1360432

    researchmap

  • Specific AAV2/PHP.eB-mediated gene transduction of CA2 pyramidal cells via injection into the lateral ventricle. 国際誌

    Kazuki Okamoto, Yuji Kamikubo, Kenta Yamauchi, Shinichiro Okamoto, Megumu Takahashi, Yoko Ishida, Masato Koike, Yuji Ikegaya, Takashi Sakurai, Hiroyuki Hioki

    Scientific reports   13 ( 1 )   323 - 323   2023年1月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Given its limited accessibility, the CA2 area has been less investigated compared to other subregions of the hippocampus. While the development of transgenic mice expressing Cre recombinase in the CA2 has revealed unique features of this area, the use of mouse lines has several limitations, such as lack of specificity. Therefore, a specific gene delivery system is required. Here, we confirmed that the AAV-PHP.eB capsid preferably infected CA2 pyramidal cells following retro-orbital injection and demonstrated that the specificity was substantially higher after injection into the lateral ventricle. In addition, a tropism for the CA2 area was observed in organotypic slice cultures. Combined injection into the lateral ventricle and stereotaxic injection into the CA2 area specifically introduced the transgene into CA2 pyramidal cells, enabling us to perform targeted patch-clamp recordings and optogenetic manipulation. These results suggest that AAV-PHP.eB is a versatile tool for specific gene transduction in CA2 pyramidal cells.

    DOI: 10.1038/s41598-022-27372-8

    PubMed

    researchmap

  • Preferential arborization of dendrites and axons of parvalbumin- and somatostatin-positive GABAergic neurons within subregions of the mouse claustrum 国際誌

    Megumu Takahashi, Tomoyo Kobayashi, Haruhi Mizuma, Kenta Yamauchi, Shinichiro Okamoto, Kazuki Okamoto, Yoko Ishida, Masato Koike, Masahiko Watanabe, Tadashi Isa, Hiroyuki Hioki

    Neuroscience Research   190   92 - 106   2022年11月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    The claustrum coordinates the activities of individual cortical areas through abundant reciprocal connections with the cerebral cortex. Although these excitatory connections have been extensively investigated in three subregions of the claustrum-core region and dorsal and ventral shell regions-the contribution of GABAergic neurons to the circuitry in each subregion remains unclear. Here, we examined the distribution of GABAergic neurons and their dendritic and axonal arborizations in each subregion. Combining in situ hybridization with immunofluorescence histochemistry showed that approximately 10% of neuronal nuclei-positive cells expressed glutamic acid decarboxylase 67 mRNA across the claustral subregions. Approximately 20%, 30%, and 10% of GABAergic neurons were immunoreactive for parvalbumin (PV), somatostatin (SOM), and vasoactive intestinal polypeptide, respectively, in each subregion, and these neurochemical markers showed little overlap with each other. We then reconstructed PV and SOM neurons labeled with adeno-associated virus vectors. The dendrites and axons of PV and SOM neurons were preferentially localized to their respective subregions where their cell bodies were located. Furthermore, the axons were preferentially extended in a rostrocaudal direction, whereas the dendrites were relatively isotropic. The present findings suggest that claustral PV and SOM neurons might execute information processing separately within the core and shell regions.

    DOI: 10.1016/j.neures.2022.11.008

    PubMed

    researchmap

  • Astrocytic cAMP modulates memory via synaptic plasticity 国際誌

    Zhiwen Zhou, Kazuki Okamoto, Junya Onodera, Toshimitsu Hiragi, Megumi Andoh, Masahito Ikawa, Kenji F. Tanaka, Yuji Ikegaya, Ryuta Koyama

    Proceedings of the National Academy of Sciences   118 ( 3 )   2021年1月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Astrocytes play a key role in brain homeostasis and functions such as memory. Specifically, astrocytes express multiple receptors that transduce signals via the second messenger cAMP. However, the involvement of astrocytic cAMP in animal behavior and the underlying glial-neuronal interactions remains largely unknown. Here, we show that an increase in astrocytic cAMP is sufficient to induce synaptic plasticity and modulate memory. We developed a method to increase astrocytic cAMP levels in vivo using photoactivated adenylyl cyclase and found that increased cAMP in hippocampal astrocytes at different time points facilitated memory formation but interrupted memory retention via NMDA receptor-dependent plasticity. Furthermore, we found that the cAMP-induced modulation of memory was mediated by the astrocyte-neuron lactate shuttle. Thus, our study unveils a role of astrocytic cAMP in brain function by providing a tool to modulate astrocytic cAMP in vivo.

    DOI: 10.1073/pnas.2016584118

    PubMed

    researchmap

  • Tb3+-doped fluorescent glass for biology

    Kazuki Okamoto, Teppei Ebina, Naoki Fujii, Kuniaki Konishi, Yu Sato, Tetsuhiko Kashima, Risako Nakano, Hiroyuki Hioki, Haruki Takeuchi, Junji Yumoto, Masanori Matsuzaki, Yuji Ikegaya

    Science Advances   7 ( 2 )   eabd2529 - eabd2529   2021年1月

     詳細を見る

    掲載種別:研究論文(学術雑誌)   出版者・発行元:American Association for the Advancement of Science (AAAS)  

    Optical investigation and manipulation constitute the core of biological experiments. Here, we introduce a new borosilicate glass material that contains the rare-earth ion terbium(III) (Tb<sup>3+</sup>), which emits green fluorescence upon blue light excitation, similar to green fluorescent protein (GFP), and thus is widely compatible with conventional biological research environments. Micropipettes made of Tb<sup>3+</sup>-doped glass allowed us to target GFP-labeled cells for single-cell electroporation, single-cell transcriptome analysis (Patch-seq), and patch-clamp recording under real-time fluorescence microscopic control. The glass also exhibited potent third harmonic generation upon infrared laser excitation and was usable for online optical targeting of fluorescently labeled neurons in the in vivo neocortex. Thus, Tb<sup>3+</sup>-doped glass simplifies many procedures in biological experiments.

    DOI: 10.1126/sciadv.abd2529

    researchmap

  • GABAergic inhibition reduces the impact of synaptic excitation on somatic excitation

    Chiaki Kobayashi, Kazuki Okamoto, Yasuhiro Mochizuki, Hidetoshi Urakubo, Kenta Funayama, Tomoe Ishikawa, Tetsuhiko Kashima, Ayako Ouchi, Agnieszka F. Szymanska, Shin Ishii, Yuji Ikegaya

    Neuroscience Research   146   22 - 35   2019年9月

     詳細を見る

    掲載種別:研究論文(学術雑誌)   出版者・発行元:Elsevier {BV}  

    The effect of excitatory synaptic input on the excitation of the cell body is believed to vary depending on where and when the synaptic activation occurs in dendritic trees and the spatiotemporal modulation by inhibitory synaptic input. However, few studies have examined how individual synaptic inputs influence the excitability of the cell body in spontaneously active neuronal networks mainly because of the lack of an appropriate method. We developed a calcium imaging technique that monitors synaptic inputs to hundreds of spines from a single neuron with millisecond resolution in combination with whole-cell patch-clamp recordings of somatic excitation. In rat hippocampal CA3 pyramidal neurons ex vivo, a fraction of the excitatory synaptic inputs were not detectable in the cell body against background noise. These synaptic inputs partially restored their somatic impact when a GABAA receptor blocker was intracellularly perfused. Thus, GABAergic inhibition reduces the influence of some excitatory synaptic inputs on the somatic excitability. Numerical simulation using a single neuron model demonstrates that the timing and locus of a dendritic GABAergic input are critical to exert this

    DOI: 10.1016/j.neures.2018.09.014

    researchmap

    その他リンク: https://www.ncbi.nlm.nih.gov/pubmed/30243908

  • Exercise Reverses Behavioral and Synaptic Abnormalities after Maternal Inflammation 査読

    Andoh M, Shibata K, Okamoto K, Onodera J, Morishita K, Miura Y, Ikegaya Y, Koyama R

    Cell Reports   27 ( 10 )   2817 - 2825.e5   2019年6月

  • Recurrent connections between CA2 pyramidal cells 査読

    Okamoto K, Ikegaya Y

    Hippocampus   29 ( 4 )   305 - 312   2019年4月

  • Immature electrophysiological properties of human-induced pluripotent stem cell-derived neurons transplanted into the mouse cortex for 7 weeks. 査読

    Kayama T, Okamoto K, Gao M, Ikegaya Y, Sasaki T

    Neuroreport   30 ( 3 )   169 - 173   2019年2月

  • GABAergic malfunction in the anterior cingulate cortex underlying maternal immune activation-induced social deficits. 査読 国際誌

    Kazuki Okamoto, Natsuko Hitora-Imamura, Hiroyuki Hioki, Yuji Ikegaya

    Journal of neuroimmunology   321   92 - 96   2018年8月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Elsevier {BV}  

    Social deficits are one of the major symptoms of psychiatric disorders, including autism spectrum disorders (ASDs) and schizophrenia. However, the underlying mechanism remains ill-defined. Here, we focused on the anterior cingulate cortex (ACC), a brain region that is related to social behaviors, of mice that received poly(I:C)-induced maternal immune activation. Offspring born from poly(I:C)-treated dams exhibited social deficits in a three-chamber task at juvenile stages. Using whole-cell patch clamp recordings, we found that layer 2/3 pyramidal cells were hyperactive in acute ACC slices prepared from poly(I:C)-treated mice compared to those from saline-treated mice. The hyperexcitation was associated with a reduction in inhibitory synapse activity. Local injection of the GABAA receptor enhancer clonazepam into the ACC of poly(I:C)-treated mice restored the social behaviors of the mice. These results suggest that the balanced excitability of ACC neurons is essential for social ability.

    DOI: 10.1016/j.jneuroim.2018.06.006

    PubMed

    researchmap

  • Ethanol facilitates socially evoked memory recall in mice by recruiting pain-sensitive anterior cingulate cortical neurons. 査読

    Sakaguchi T, Iwasaki S, Okada M, Okamoto K, Ikegaya Y

    Nature communications   9 ( 1 )   3526   2018年8月

     詳細を見る

    Alcohol is a traditional social-bonding reinforcer; however, the neural mechanism underlying ethanol-driven social behaviors remains elusive. Here, we report that ethanol facilitates observational fear response. Observer mice exhibited stronger defensive immobility while observing cagemates that received repetitive foot shocks if the observer mice had experienced a brief priming foot shock. This enhancement was associated with an observation-induced recruitment of subsets of anterior cingulate cortex (ACC) neurons in the observer mouse that were responsive to its own pain. The vicariously activated ACC neurons projected their axons preferentially to the basolateral amygdala. Ethanol shifted the ACC neuronal balance toward inhibition, facilitated the preferential ACC neuronal recruitment during observation, and enhanced observational fear response, independent of an oxytocin signaling pathway. Furthermore, ethanol enhanced socially evoked fear response in autism model mice.

    DOI: 10.1038/s41467-018-05894-y

    PubMed

    researchmap

    その他リンク: http://orcid.org/0000-0003-1575-6030

  • Hippocampal ripples down-regulate synapses. 査読 国際誌

    Hiroaki Norimoto, Kenichi Makino, Mengxuan Gao, Yu Shikano, Kazuki Okamoto, Tomoe Ishikawa, Takuya Sasaki, Hiroyuki Hioki, Shigeyoshi Fujisawa, Yuji Ikegaya

    Science (New York, N.Y.)   359 ( 6383 )   1524 - 1527   2018年3月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:American Association for the Advancement of Science ({AAAS})  

    The specific effects of sleep on synaptic plasticity remain unclear. We report that mouse hippocampal sharp-wave ripple oscillations serve as intrinsic events that trigger long-lasting synaptic depression. Silencing of sharp-wave ripples during slow-wave states prevented the spontaneous down-regulation of net synaptic weights and impaired the learning of new memories. The synaptic down-regulation was dependent on the N-methyl-d-aspartate receptor and selective for a specific input pathway. Thus, our findings are consistent with the role of slow-wave states in refining memory engrams by reducing recent memory-irrelevant neuronal activity and suggest a previously unrecognized function for sharp-wave ripples.

    DOI: 10.1126/science.aao0702

    PubMed

    researchmap

  • 3-Hz subthreshold oscillations of CA2 neurons In vivo 査読

    Nobuyoshi Matsumoto, Kazuki Okamoto, Yuki Takagi, Yuji Ikegaya

    HIPPOCAMPUS   26 ( 12 )   1570 - 1578   2016年12月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1002/hipo.22657

    Web of Science

    PubMed

    researchmap

  • Homeostatic Hippocampal Activity against Reduced Glutamatergic Neurotransmission 査読

    Tomoe Ishikawa, Kazuki Okamoto, Yuji Ikegaya

    INTERNATIONAL JOURNAL OF PHARMACOLOGY   11 ( 4 )   318 - 326   2015年

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.3923/ijp.2015.318.326

    Web of Science

    researchmap

  • Ex vivo cultured neuronal networks emit in vivo-like spontaneous activity. 査読

    Kazuki Okamoto, Tomoe Ishikawa, Reimi Abe, Daisuke Ishikawa, Chiaki Kobayashi, Mika Mizunuma, Hiroaki Norimoto, Norio Matsuki, Yuji Ikegaya

    The journal of physiological sciences : JPS   64 ( 6 )   421 - 31   2014年11月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Spontaneous neuronal activity is present in virtually all brain regions, but neither its function nor spatiotemporal patterns are fully understood. Ex vivo organotypic slice cultures may offer an opportunity to investigate some aspects of spontaneous activity, because they self-restore their networks that collapsed during slicing procedures. In hippocampal networks, we compared the levels and patterns of in vivo spontaneous activity to those in acute and cultured slices. We found that the firing rates and excitatory synaptic activity in the in vivo hippocampus are more similar to those in slice cultures compared to acute slices. The soft confidence-weighted algorithm, a machine learning technique without human bias, also revealed that hippocampal slice cultures resemble the in vivo hippocampus in terms of the overall tendency of the parameters of spontaneous activity.

    DOI: 10.1007/s12576-014-0337-4

    PubMed

    researchmap

▶ 全件表示

MISC

  • テルビウムドープガラスの蛍光を手がかりにした標的パッチクランプ法

    岡本和樹, 藤井直樹, 蝦名鉄平, 小西邦昭, 佐藤由宇, 中野利沙子, 日置寛之, 山口瞬, 竹内春樹, 湯本潤司, 松崎政紀, 池谷裕二

    日本薬学会年会要旨集(CD-ROM)   139th   ROMBUNNO.23O‐pm14S   2019年

     詳細を見る

    記述言語:日本語  

    J-GLOBAL

    researchmap

  • Corrigendum: 3-Hz Subthreshold Oscillations of CA2 Neurons In Vivo (vol 26, pg 1570, 2016)

    Nobuyoshi Matsumoto, Kazuki Okamoto, Yuki Takagi, Yuji Ikegaya

    HIPPOCAMPUS   27 ( 1 )   111 - 111   2017年1月

     詳細を見る

  • Empathic deficits in a mouse model of autism spectrum disorder

    Tetsuya Sakaguchi, Yuji Ikegaya, Satoshi Iwasaki, Kazuki Okamoto

    INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY   19   292 - 293   2016年6月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)  

    Web of Science

    researchmap

受賞

  • IDDI小幡賞

    2023年11月   イノベーション創薬研究所  

     詳細を見る

共同研究・競争的資金等の研究

  • 長軸へ拡張した海馬神経回路解析

    研究課題/領域番号:22K15230

    2022年4月 - 2025年3月

    制度名:科学研究費助成事業

    研究種目:若手研究

    提供機関:日本学術振興会

    岡本 和樹

      詳細を見る

    配分額:4550000円 ( 直接経費:3500000円 、 間接経費:1050000円 )

    researchmap

  • 大脳皮質パルブアルブミン発現細胞ネットワークの結合則

    研究課題/領域番号:20K16112

    2020年4月 - 2022年3月

    制度名:科学研究費助成事業

    研究種目:若手研究

    提供機関:日本学術振興会

    岡本 和樹

      詳細を見る

    配分額:4290000円 ( 直接経費:3300000円 、 間接経費:990000円 )

    脳回路を構成する神経細胞の一部はGABA作動性細胞であり、回路の抑制を担う。これらシナプス結合の測定には形態学と生理学の双方からのアプローチが要求されるが、GABAを介した抑制性シナプスの場合、生理的に測定できる範囲に限界があり、未解明な部分も多い。本研究は、形態学手法と生理学手法を組み合わせ、軸索形態の「てがかり」からGABA細胞、特にパルブアルブミン発現細胞(PV細胞)の生理的結合を予測できるモデルを構築することを目的とした。生理測定で得られたシナプス入力を形態的なシナプス位置に基づいて解析することで、結合形成のパターン抽出、およびシナプス強度の算出を行った。

    researchmap

  • 海馬CA2野再帰回路の機能解明

    研究課題/領域番号:19J01590

    2019年4月 - 2022年3月

    制度名:科学研究費助成事業

    研究種目:特別研究員奨励費

    提供機関:日本学術振興会

    岡本 和樹

      詳細を見る

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

    海馬にはCA2野という異質な亜領域がある。CA2野の独自性は近年注目を集めるようになったが、他の領域と比べてあまり研究されてこなかった背景がある。本研究では、研究代表者自身が過去に発見したCA2野の再起回路構造に着目している。この回路構造は海馬では珍しく、従来CA3野にしか存在しないと考えられてきた。現状、再帰回路と機能の因果性を直接示した研究はないものの、CA3野が担う学習や記憶に関連した機能を持つものとされている。これはCA2野にも当てはまるのかは定かではない。そこで、新たに発見したCA2野の再起回路がCA3野と類似した機能を持つのか、あるいは独自の機能を持つのかを解明することを目的とする。CA2野は小さな領域であるため、実験的なアプローチが難しい。また、再起回路というシナプス結合の検出・操作にも電気生理学的、形態学的な手法を要する。
    そこで本年度は、海馬CA2野を優先して標識するツールを発見した。これは従来のCre/loxPシステムと遺伝子組み換えマウスを用いた手法とは異なるアプローチであり、野生型マウスに対してCA2特異的な操作を可能とするものである。さらに、この手法によって、当初の課題であった海馬CA2錐体細胞へのスパースな遺伝子導入を実現することができた。現在はCA2錐体細胞の一部にだけチャネルロドプシンを発現させることで、未発現細胞をコントロールとしながら、CA2内部のシナプス結合性の検証を進めている。海馬CA2野を標識するツールについても並行して論文発表を準備中である。

    researchmap

  • 海馬CA3野における神経回路基盤の解明

    研究課題/領域番号:16J07503

    2016年4月 - 2019年3月

    制度名:科学研究費助成事業

    研究種目:特別研究員奨励費

    提供機関:日本学術振興会

    岡本 和樹

      詳細を見る

    配分額:3400000円 ( 直接経費:3400000円 )

    申請研究では、海馬神経細胞の正確なシナプス結合確率およびシナプス強度の測定を目的とした。そうした内在的な結合性のもと、海馬がもっとも効率化された記憶容量と処理能力を持つかを検証した。ひとつひとつのシナプスのつながりは微弱なため、その手段として、単一細胞の活動を記録・制御するパッチクランプ法を複数の神経細胞から同時におこなう必要があった。再帰性シナプス結合の評価のためには数百もの細胞ペアのデータ収集が要求されるが、これまでは設備の関係上2つの細胞からの同時記録が限界であり、データ収集効率の悪さが課題であった。前年度において、国内初となる6つの細胞から記録できる設備を立ち上げ、同時に30もの細胞ペアからパッチクランプ記録が可能となった。申請者はこの技量を向上させ、海馬からの大規模なシナプス回路解析を行った。海馬の亜領域の中には、CA2野という領域が存在する。近年社会記憶などの独自の機能が発見され注目を集めるようになったCA2領域であるが、その神経回路は未知の部分が多い。海馬の計算論を語る上で、CA3の再帰回路は重要な位置づけにあるが、そもそも海馬CA2に再帰回路が存在するのかどうかは長らく謎であった。申請者は海馬CA2野から500ペアの記録に成功し、海馬CA2野の再帰回路を新たに発見した。また、CA1野およびCA3野からの再帰回路シナプス測定も行い、CA2野の神経回路がもつ特徴を見出した。この成果はHippocampus誌に受理された。

    researchmap