2024年
原著論文
- Takewaki D, Kiguchi Y, Masuoka H, Manu M, Raveney BJE, Narushima S, Kurokawa R, Ogata Y, Kimura Y, Sato N, Ozawa Y, Yagishita S, Araki T, Miyake S, Sato W, Suda W, Yamamura T..
Tyzzerella nexilis strains enriched in mobile genetic elements are involved in progressive multiple sclerosis .
Cell Reports 43: 114785, 2024.
- Ho WJ, Marinova MB, Listijono DR, Bertoldo MJ, Richani D, Kim LJ, Brown A, Riepsamen AH, Cabot S, Frost ER, Bustamante S, Zhong L, Selesniemi K, Wong D, Madawala R, Marchante M, Goss DM, Li C, Araki T, Livingston DJ, Turner N, Sinclair DA, Walters KA, Homer HA, Gilchrist RB, Wu LE..
Fertility protection during chemotherapy treatment by boosting the NAD(P)+ metabolome.
EMBO Mol Med 16: 2583 - 2618, 2024.
- Hagihara H, Shoji H, Hattori S, Sala G, Takamiya Y, Tanaka M, Ihara M, Shibutani M, Hatada I, Hori K, Hoshino M, Nakao A, Mori Y, Okabe S, Matsushita M, Urbach A, Katayama Y, Matsumoto A, Nakayama KI, Katori S, Sato T, Iwasato T, Nakamura H, Goshima Y, Raveau M, Tatsukawa T, Yamakawa K, Takahashi N, Kasai H, Inazawa J, Nobuhisa I, Kagawa T, Taga T, Darwish M, Nishizono H, Takao K, Sapkota K, Nakazawa K, Takagi T, Fujisawa H, Sugimura Y, Yamanishi K, Rajagopal L, Hannah ND, Meltzer HY, Yamamoto T, Wakatsuki S, Araki T, Tabuchi K, Numakawa T, Kunugi H, Huang FL, Hayata-Takano A, Hashimoto H, Tamada K, Takumi T, Kasahara T, Kato T, Graef IA, Crabtree GR, Asaoka N, Hatakama H, Kaneko S, Kohno T, Hattori M, Hoshiba Y, Miyake R, Obi-Nagata K, Hayashi-Takagi A, Becker LJ, Yalcin I, Hagino Y, Kotajima-Murakami H, Moriya Y, Ikeda K, Kim H, Kaang BK, Otabi H, Yoshida Y, Toyoda A, Komiyama NH, Grant SGN, Ida-Eto M, Narita M, Matsumoto KI, Okuda-Ashitaka E, Ohmori I, Shimada T, Yamagata K, Ageta H, Tsuchida K, Inokuchi K, Sassa T, Kihara A, Fukasawa M, Usuda N, Katano T, Tanaka T, Yoshihara Y, Igarashi M, Hayashi T, Ishikawa K, Yamamoto S, Nishimura N, Nakada K, Hirotsune S, Egawa K, Higashisaka K, Tsutsumi Y, Nishihara S, Sugo N, Yagi T, Ueno N, Yamamoto T, Kubo Y, Ohashi R, Shiina N, Shimizu K, Higo-Yamamoto S, Oishi K, Mori H, Furuse T, Tamura M, Shirakawa H, Sato DX, Inoue YU, Inoue T, KomineY, Yamamori T, Sakimura K, Miyakawa T.
Large-scale animal model study uncovers altered brain pH and lactate levels as a transdiagnostic endophenotype of neuropsychiatric disorders involving cognitive impairment.
eLife 12, RP89376, 2024.
総説・著書
2023年
原著論文
- Zhang S, Ohkawara B, Ito M, Huang Z, Zhao F, Nakata T, Takeuchi T, Sakurai H, Komaki H, Kamon M, Araki T, Ohno K.
A mutation in DOK7 in congenital myasthenic syndrome forms aggresome in cultured cells, and reduces DOK7 expression and MuSK phosphorylation in patient-derived iPS cells.
Hum Mol Genet 32: 1511–1523, 2023.
2022年
原著論文
- Nakazawa E, Fukushi T, Tachibana K, Uehara R, Arie F, Akter N, Maruyama M, Morita K, Araki T, Sadato N.
The way forward for neuroethics in Japan: A review of five topics surrounding present challenges.
Neuroscience Research,183:7-16, 2022.
- Hashimoto Y, Kuniishi H, Sakai K, Fukushima Y, Du X , Yamashiro K, Hori K, Imamura M, Hoshino M, Yamada M, Araki T, Itaka K, Sakagami H, Takeda S, Itaka K, Ichinohe N, Muntoni F, Sekiguchi M, Aoki Y.
Brain Dp140 alters glutamatergic transmission and social behaviour in the mdx52 mouse model of Duchenne muscular dystrophy.
Progress in Neurobiology 216: 102288, 2022.
- Nakamori M, Shimizu H, Ogawa K, Hasuike Y, Nakajima T, Sakurai H, Araki T, Okada Y, Kakita A, Mochizuki H.
Cell type-specific abnormalities of central nervous system in myotonic dystrophy type 1.
Brain Communications 4(3):fcac154, 2022.
総説・著書
2021年
主な研究成果
原著論文
- Koike S, Tanaka SC, Okada T, Aso T, Yamashita A, Yamashita O, Asano M, Maikusa N, Morita K, Okada N, Fukunaga M, Uematsu A, Togo H, Miyazaki A, Murata K, Urushibata Y, Autio J, Ose T, Yoshimoto J, Araki T, Glasser MF, Van Essen DC, Maruyama M, Sadato N, Kawato M, Kasai K, Okamoto Y, Hanakawa T, Hayashi T; Brain/MINDS Beyond Human Brain MRI Group.
Brain/MINDS beyond human brain MRI project: A protocol for multi-level harmonization across brain disorders throughout the lifespan
NeuroImage: Clinical 8:102600, 2021.
- Uezumi A, Ikemoto-Uezumi M, Zhou H, Kurosawa T, Yoshimoto Y, Nakatani M, Hitachi K, Yamaguchi H, Wakatsuki S, Araki T, Morita M, Yamada H, Toyoda M, Kanazawa N, Nakazawa N, Hino J, Fukada S, Tsuchida K.
Mesenchymally expressed Bmp3b maintains skeletal muscle integrity and reduction of its expression contributes to sarcopenia.
Journal of Clinical Investigation. 131(1) e139617, 2021.
総説・著書
2020年
主な研究成果
原著論文
- Nagano S, Jinno J, Abdelhamid RF, Jin Y, Shibata M, Watanabe S, Hirokawa S, Nishizawa M, Sakimura K, Onodera O, Okada H, Okada T, Saito Y, Takahashi-Fujigasaki J, Murayama S, Wakatsuki S, Mochizuki H, Araki T.
TDP-43 transports ribosomal protein mRNA to regulate axonal local translation in neuronal axons.
Acta Neuropathologica. 140(5):695-713, 2020.
- Bertoldo MJ, Listijono DR, Ho WJ, Riepsamen AH, Goss DM, Richani D, Jin XL, Mahbub S, Campbell JM, Habibalahi A, Loh WN, Youngson NA, Maniam J, Wong ASA, Selesniemi K, Bustamante S, Li C, Zhao Y, Marinova MB, Kim LJ, Lau L, Wu RM, Mikolaizak AS, Araki T, Le Couteur DG, Turner N, Morris MJ, Walters KA, Goldys E, O'Neill C, Gilchrist RB, Sinclair DA, Homer HA, Wu LE.
NAD+ repletion rescues female fertility during reproductive aging.
Cell Reports. Volume 30, February 2020, Pages 1670-1681
- Huang K, Masuda A, Chen G, Bushra S, Kamon M, Araki T, Kinoshita M, Ohkawara B, Ito M, Ohno K.
Inhibition of cyclooxygenase-1 by nonsteroidal anti-inflammatory drugs demethylates MeR2 enhancer and promotes Mbnl1 transcription in myogenic cells.
Scientific Reports. Volume 10, February 2020, Pages 2558
総説・著書
- 栁下聡介
閉塞性睡眠時無呼吸とアルツハイマー病との関係
オベリスク No.25 issue 1, Jan, 2020.
- 栁下聡介
閉塞性睡眠時無呼吸と認知機能低下
THE LUNG perspectives No.28 issue 1, Feb, 2020.
2019年
原著論文
- Numata-Uematsu Y, Wakatsuki S, Nagano S, Shibata M, Sakai K, Ichinohe N, Mikoshiba K, Ohshima T, Yamashita N, Goshima Y, Araki T.
Inhibition of collapsin response mediator protein-2 phosphorylation ameliorates motor phenotype of ALS model mice expressing SOD1G93A.
Neuroscience Research Volume 139, February 2019, Pages 63-68
- Takahashi Y, Uchino A, Shioya A, Sano T, Matsumoto C, Numata-Uematsu Y, Nagano S, Araki T, Murata M, Murayama S, Saito Y.
Altered immunoreactivity of ErbB4, a causative gene product for ALS19.
Neuropathology 39: 268-278, 2019.
- Tsubota M, Fukuda R, Hayashi Y, Miyazaki T, Ueda S, Yamashita R, Koike N, Sekiguchi F, Wake H, Wakatsuki S, Ujiie Y, Araki T, Nishibori M, Kawabata A.
Role of non-macrophage cell-derived HMGB1 in oxaliplatin-induced peripheral neuropathy and its prevention by the thrombin/thrombomodulin system in rodents: negative impact of anticoagulants.
J Neuroinflammation 16(1):199, 2019.
総説・著書
- Toshiyuki Araki
Regulatory Mechanism of Peripheral Nerve Myelination by Glutamate-Induced Signaling.
Myelin Advances in Experimental Medicine and Biology No.1190 pp 23-31, November, 2019.
- 氏家悠佳, 若月修二, 荒木敏之
低酸素応答による末梢神経の髄鞘形成制御
日本応用酵素協会誌No.53 pp 27-32, Mar, 2019.
- 荒木 敏之
神経軸索変性メカニズムの研究と神経保護的疾患治療法の開発
「公益財団法人テルモ生命科学芸術財団 30周年記念誌」 pp 48-49.
- 荒木 敏之
神経変性・神経発達障害発症メカニズムにおける腸内細菌叢の寄与に関する研究
「ヤクルト・バイオサイエンス研究財団 年報」令和元年(2019年)版 pp 33-38.
2018年
総説・著書
- Toshiyuki Araki, Masayoshi Kamon, Hidetoshi Sakurai
「Disease Modeling and Drug Development with DM1 Patient-Derived iPS Cells」
「Myotonic Dystrophy~Disease Mechanism, Current Management and Therapeutic Development」 pp 189-201. Ed by Masanori Takahashi, Tsuyoshi Matsumura. Springer, 2018
- 栁下聡介
「神経変性疾患では細胞内外に異常蛋白質が蓄積する」
「カラー図解 人体の細胞生物学 」 pp 254-255. 編者 坂井建雄. 石崎泰樹. 日本医事新報社, 2018
- Yagishita S
「Chapter 7:Co-immunoprecipitation Assay to Investigate the Interaction Strength Between Synaptic Proteins Using COS-7 Cells」
「Co-Immunoprecipitation Methods for Brain Tissue」 pp 89-96. Ed by Yuji Odagaki, Dasiel O. Borroto-Escuela. Springer, 2018
2017年
主な研究成果
総説・著書
- 荒木敏之「末梢神経の髄鞘化制御メカニズム」
末梢神経 28巻1号 Page 16-22 日本末梢神経学会、名古屋 2017年
- 荒木敏之、若月修二「神経軸索変性の分子メカニズム」
Dementia Japan 31巻2号 Page 252-257、 日本認知症学会 2017年
原著論文
- Imai S, Koyanagi M, Azimi Z, Nakazato Y, Matsumoto M, Ogihara T, Yonezawa A, Omura T, Nakagawa S, Wakatsuki S, Araki T, Kaneko S, Matsubara K.
Taxanes and platinum derivatives impair Schwann cells prior to induction of neurotoxicity via distinct mechanisms.
Sci Rep 7: 5947 (2017)
- Ueki J, Nakamori M, Nakamura M, Nishikawa M, YoshidaY, Tanaka A, Morizane A, Kamon M, Araki T, Takahash MP, Watanabe A, Inagaki N,Sakurai H.
Myotonic dystrophy type 1 patient-derived iPSCs for the investigation of CTG repeat instability.
Sci Rep 7: 42522 (2017)
2016年
総説・著書
- 荒木敏之「ミトコンドリア機能と末梢神経障害」
末梢神経 27巻2号 Page151-153 日本末梢神経学会、名古屋 2016年
- 若月修二、荒木敏之「酸化ストレスを神経変性に変換する仕組み:鍵分子ZNRF1の活性化メカニズムと変性する軸索におけるオートファジー誘導」
臨床免疫・アレルギー科66(4): 337-344 東京 科学評論社 2016年
- 荒木敏之、畠山英之、武田伸一「疾患特異的iPS細胞を活用した筋疾患研究」
実験医学 34(4):535-539、2016年
- Seiichi Nagano, Toshiyuki Araki「Role of Cysteine Residue of Mutant Cu, Zn-superoxide Dismutase (SOD1) in the Pathogenesis of Amyotrophic Lateral Sclerosis (ALS)」
「Novel Aspects of Amyotrophic Lateral Sclerosis」page 87-100
Humberto Foyaca Sibat;Lurdes de Fatima Ibanez Valdes編、「Update on Amyotrophic Lateral Sclerosis」INTECH(Croatia)2016年
ISBN 978-953-51-2601-0
原著論文
- Takahashi Y, Kanai M, Taminato T, Watanabe S, Matsumoto C, Araki T, Okamoto T, Ogawa M, Murata M.
Compound heterozygous intermediate MJD alleles cause cerebellar ataxia with sensory neuropathy.
Neurol Genet. 3(1): e123 (2016)
- Saito F, Wakatsuki S, Tokunaga S, Araki T.
Glutamate signals through mGluR2 to control Schwann cell differentiation and proliferation.
Sci. Rep. 6,: 29856 (2016)
- Wakatsuki S, Araki T.
NADPH oxidases promote apoptosis by activating ZNRF1 ubiquitin ligase in neurons treated with an exogenously applied oxidant.
Communicative & Integrative Biology 9(2) e1143575 (2016)
2015年
主な研究成果
総説・著書
- Shuji Wakatsuki, Toshiyuki Araki
「Significance of Mechanism-Oriented Research Toward Neuronal Protection Therapy Against Neurodegenerative Disorders ~ ZNRF1 E3 Ubiquitin Ligase as a Critical Mediator for Wallerian Degeneration and Neuronal Apoptosis」
「Neurodegenerative Disorders as Systemic Diseases 」 pp 159-182. Ed by Keiji Wada Springer, 2015
原著論文
2014年
原著論文
- Oie S, Matsuzaki K, Yokoyama W, Tokunaga, S, Waku T, Han SI, Iwasaki N, Mikogai A, Yasuzawa-Tanaka K, Hiyoshi H, Nakajima Y, Araki T, Kimura K, Yanagisawa J, Murayama A.
Hepatic rRNA Transcription Regulates High-Fat Diet-Induced Obesity.
Cell Reports 7(3): 807–820 (2014)
- Wakatsuki S, Araki T, Sehara A.
Neuregulin-1/Glial Growth Factor stimulates Schwann Cell Migration by inducing the alpha5beta1 integrin–ErbB2–Focal Adhesion Kinase Complex Formation.
Genes Cell 19(1):66-77 (2014)
2013年
原著論文
- Togashi K, Wakatsuki S, Furuno A, Tokunaga S, Nagai Y, Araki, T.
Na+/H+ exchangers induce autophagy in neurons and inhibit polyglutamine-induced
aggregate formation.
PLoS One 8(11):e81313 (2013)
- Park JY, Jang SY, Shin YK, Koh H, Suh DJ, Tokunaga S, Araki T, Park HT.
Mitochondrial swelling and microtubule depolymerization are associated with energy depletion in axon degeneration.
Neuroscience. 238:258-269 (2013)
総説・著書
- 荒木敏之「神経軸索の変性からの保護と再生」
末梢神経 Vol 24, No.2 pp205-209 2013年 日本末梢神経学会、名古屋
2012年
原著論文
総説・著書
- 徳永慎治,荒木敏之「NAD合成経路改変によるミトコンドリア障害からの神経保護」
実験医学 Vol 30, No.9 pp1418-1422 2012年 羊土社、東京
- 若月修二,荒木敏之 「ユビキチン・プロテアソーム系によって制御される軸索変性の分子メカニズム」
生化学 Vol 84, No.6 pp463-471 2012年 日本生化学会、東京
2011年
主な研究成果
原著論文
2010年
原著論文
2009年
主な研究成果
原著論文
- Kabuta T, Kinugawa A, Tsuchiya Y, Kabuta C, Setsuie R, Tateno M, Araki T, Wada K,
Familial amyotrophic lateral sclerosis-linked mutant SOD1 aberrantly
interacts with tubulin.
Biochem. Biophys. Res. Commun., 387:121-126, 2009
- Takada H, Kawana T, Ito Y, Kikuno RF, Mamada H, Araki T,
Koga H, Asashima M, Taira M.
The RNA binding protein Mex3b has a fine-tuning system for mRNA regulation in early Xenopus development.
Development 136:2413-2422, 2009
- Yahata N, Yuasa S, Araki T.
NMNAT expression in mitochondrial matrix delays Wallerian degeneration.
J. Neurosci. 29: 6276-6284, 2009
- Wakatsuki S, Yumoto N, Komatsu K, Araki T, Sehara A.
Roles of meltrin beta/ADAM19 in progression of Schwann cell differentiation and myelination during sciatic nerve regeneration.
J. Biol.Chem. 284: 2957-2966, 2009
- Tateno M, Kato S, Sakurai T, Nukina N, Takahashi R, Araki T.
Mutant SOD1 impairs axonal transport of choline acetyltransferase and acetylcholine release by sequestering KAP3.
Hum Mol Genet 18: 942-955, 2009
総論・著書
- 荒木敏之,八幡直樹 「神経軸索の変性と神経回路の修復」
脳21 Vol 12, No.3 pp300-305 2009年 金芳堂、京都
2008年度
主な研究成果
~2007年度
原著論文
総説・著書