mitochondria diary

ミトコンドリア病の治療法研究開発のための学術情報収集とシェア

2023-01-01から1ヶ月間の記事一覧

エンパグリフロジンは、Wnt/β-カテニンを活性化して、3型心腎症候群に対するFUNDC1依存性ミトコンドリア品質監視を刺激

” [HTML] Empagliflozin activates Wnt/β-catenin to stimulate FUNDC1-dependent mitochondrial quality surveillance against type-3 cardiorenal syndrome C Cai, F Wu, B Zhuang, Q Ou, X Peng, N Shi… - Molecular …, 2022 - Elsevier … Mitochondrial …

Wnt/β-カテニン/RAS シグナル伝達は、加齢に伴う腎線維症を媒介し、ミトコンドリアの機能不全と関連

” Wnt/β‐catenin/RAS signaling mediates age‐related renal fibrosis and is associated with mitochondrial dysfunction J Miao, J Liu, J Niu, Y Zhang, W Shen, C Luo, Y Liu… - Aging cell, 2019 - Wiley Online Library … 2.7 Wnt/β-catenin/RAS axis …

ミトコンドリアのATP産生障害は、小胞体ストレス誘導を介してWntシグナル伝達をダウンレギュレートする

” [HTML] Impaired mitochondrial ATP production downregulates Wnt signaling via ER stress induction R Costa, R Peruzzo, M Bachmann, G Dalla Monta… - Cell reports, 2019 - Elsevier … a generated zebrafish model lead to reduced Wnt signaling. …

哺乳動物細胞におけるミトコンドリア DNA 編集の課題: 心血管疾患の治療に焦点を当てる

” [HTML] Challenges of mitochondrial DNA editing in mammalian cells: focus on treatment of cardiovascular disease VA Khotina, M Bagheri Ekta, MS Baig, WK Wu… - Vessel Plus, 2022 Atherosclerosis is the major cause of occurrence and developm…

ミトコンドリア病患者の線維芽細胞におけるコエンザイム Q10 の総型および還元型/酸化型

” [HTML] Total and reduced/oxidized forms of coenzyme Q10 in fibroblasts of patients with mitochondrial disease C Watanabe, H Osaka, M Watanabe, A Miyauchi… - Molecular Genetics and …, 2023 … We studied fibroblasts from 24 patients with mi…

神経疾患におけるフェロトーシスの役割

” Role of ferroptosis in neurological diseases MY Yao, T Liu, L Zhang, MJ Wang, Y Yang, J Gao - Neuroscience Letters, 2021 - Elsevier … syndromes with associated epilepsy, which supports the continued clinical evaluation ofEPI-743 as a the…

ヒ素は、ミトコンドリアROS-オートファジー-リソソーム経路を介して膵臓機能障害とフェロトーシスを誘発

” Arsenic induces pancreatic dysfunction and ferroptosis via mitochondrial ROS-autophagy-lysosomal pathway S Wei, T Qiu, X Yao, N Wang, L Jiang, X Jia… - Journal of hazardous …, 2020 - Elsevier … of ferroptosis on pancreatic dysfunction tr…

フェロトーシス ferroptosis のミトコンドリア調節

” Mitochondrial regulation of ferroptosis B Gan - Journal of Cell Biology, 2021 - rupress.org … processes in mitochondria that actively drive ferroptosis, discuss recently discoveredmitochondria-… Therefore, this study proposes that mitoch…

Nrf2誘導はフリードライヒ運動失調症のフェロプトーシスを防ぐ

” [HTML] The Nrf2 induction prevents ferroptosis in Friedreich's Ataxia P La Rosa, S Petrillo, R Turchi, F Berardinelli… - Redox biology, 2021 - Elsevier … As additional indicators of ferroptosis, we further analysed the FRDA mitochondrial…

Ferroptosis フェロトーシスは神経変性疾患においてミトコンドリアによって調節される

” Ferroptosis is regulated by mitochondria in neurodegenerative diseases J Zhou, Y Jin, Y Lei, T Liu, Z Wan, H Meng… - … Diseases, 2020 - karger.com … in neurodegenerative diseases. Key Messages: … of ferroptosis, we conclude that mitochon…

Ferroptosis および癌: ミトコンドリアは「鉄の乙女」の細胞死を満たす

Ferroptosis and cancer: mitochondria meet the “iron maiden” cell death AM Battaglia, R Chirillo, I Aversa, A Sacco, F Costanzo… - Cells, 2020 - mdpi.com … This strongly suggests that ferroptosis may act as an adaptive response to … mitocho…

Ferroptosis フェロトーシスにおけるミトコンドリア調節

" Mitochondria regulation in ferroptosis H Wang, C Liu, Y Zhao, G Gao - European journal of cell biology, 2020 - Elsevier … some oxidative stress diseases, including neurodegenerative … , the pertinence betweenmitochondria and ferroptosis …

OMA1を介した統合ストレス応答は、ミトコンドリア心筋症のフェロトーシス ferroptosis から保護

" [HTML] OMA1-mediated integrated stress response protects against ferroptosis in mitochondrial cardiomyopathy S Ahola, PR Mejías, S Hermans, S Chandragiri… - Cell Metabolism, 2022 - Elsevier … the heart, ultimately culminating in ferropto…

フェロトーシス ferroptosisを標的とする:ミトコンドリア病関連てんかんの治療のための新しい治療戦略

" [HTML] Targeting ferroptosis: A novel therapeutic strategy for the treatment of mitochondrial disease-related epilepsy AH Kahn-Kirby, A Amagata, CI Maeder, JJ Mei… - PLoS …, 2019 - journals.plos.org … that ferroptosis contributes to the …

ミトコンドリア病遺伝学の最新情報: 原発性ミトコンドリア病の分子診断と拡大する表現型に関する最近の洞察

" Mitochondrial disease genetics update: recent insights into the molecular diagnosis and expanding phenotype of primary mitochondrial disease EM McCormick, Z Zolkipli-Cunningham… - Current Opinion in …, 2018 - journals.lww.com … technolog…

遺伝子編集剤の治療的 in vivo 送達

" Therapeutic in vivo delivery of gene editing agents A Raguram, S Banskota, DR Liu - Cell, 2022 - Elsevier … Editing of mitochondrial DNA is challenged by the lack of efficient methods to deliver guideRNAs into mitochondria, precluding th…

ミトコンドリア塩基編集者は、実質的な核のオフターゲット変異を誘導

" Mitochondrial base editor induces substantial nuclear off-target mutations Z Lei, H Meng, L Liu, H Zhao, X Rao, Y Yan, H Wu… - Nature, 2022 - nature.com … Mutations in mitochondrial DNA (mtDNA) are known to be associated with most adult-…

TALEN媒介ミトコンドリアゲノム編集による細胞質雄性不稔の治癒

" Curing cytoplasmic male sterility via TALEN-mediated mitochondrial genome editing T Kazama, M Okuno, Y Watari, S Yanase, C Koizuka… - Nature plants, 2019 - nature.com … to cure mitochondrial diseases 7,8 . In these studies, disease-causi…

CRISPR-Cas9 システム: 遺伝子編集の新たな夜明け

" CRISPR-Cas9 system: A new-fangled dawn in gene editing D Gupta, O Bhattacharjee, D Mandal, MK Sen, D Dey… - Life sciences, 2019 - Elsevier … an N terminal Mitochondrial targeting sequence (MTS) to direct its transport to the mitochondria…

細菌のシチジンデアミナーゼ毒素により、CRISPRフリーのミトコンドリア塩基編集が可能

" A bacterial cytidine deaminase toxin enables CRISPR-free mitochondrial base editing BY Mok, MH de Moraes, J Zeng, DE Bosch, AV Kotrys… - Nature, 2020 - nature.com … double-strand breaks, a capability that has the potential to model mitoc…

mtDNAヘテロプラスミーレベルとコピー数は、m.3243A>Gミトコンドリア病の疾患負荷を示す

" mt DNA heteroplasmy level and copy number indicate disease burden in m. 3243A> G mitochondrial disease JP Grady, SJ Pickett, YS Ng, CL Alston… - EMBO molecular …, 2018 - embopress.org … We thank the patients who participated in this stud…

ミトコンドリア病治療薬の開発

" Drug development for the therapy of mitochondrial diseases V Weissig - Trends in molecular medicine, 2020 - Elsevier … TAK-831, an inhibitor of D-amino acid oxidase, is being tested as an intervention forFriedreich’s ataxia, a mitochondr…

ミトコンドリア病の新たな治療法

" Emerging therapies for mitochondrial diseases M Hirano, V Emmanuele, CM Quinzii - Essays in biochemistry, 2018 - portlandpress.com … CoQ10 Children with mitochondrial diseases with mtDNA mutations or specific OXPHOScomplexes defects Phas…

ミトコンドリアのゲノム編集は病原性 mtDNA 変異を in vivo で修正する

" Genome editing in mitochondria corrects a pathogenic mtDNA mutation in vivo PA Gammage, C Viscomi, ML Simard, ASH Costa… - Nature medicine, 2018 - nature.com … mitochondrial disease, bearing the point mutation m.5024C>T in … disease-rele…

ミトコンドリア病: オルガネラストレス応答の病態への寄与

" Mitochondrial diseases: the contribution of organelle stress responses to pathology A Suomalainen, BJ Battersby - Nature reviews Molecular cell biology, 2018 - nature.com … mitochondrial DNA (mtDNA) maintenance and mitochondrial translat…

オミクス時代のミトコンドリア医学

" Mitochondrial medicine in the omics era J Rahman, S Rahman - The Lancet, 2018 - Elsevier … , and mitochondrial dynamics (table 1). Conversely, dozens of mitochondrial disease mutations… describing mitochondrial disease mutations (collate…

ミトコンドリア病の分子診断へのゲノムアプローチの進歩

" Advancing genomic approaches to the molecular diagnosis of mitochondrial disease SL Stenton, H Prokisch - Essays in Biochemistry, 2018 - portlandpress.com … clinical presentation, are uncommon in mitochondrial disease making the selectio…

mt-tRNA変異に起因するミトコンドリア病モデリングの進歩:皿の中の患者の脳

" [HTML] Advances in mt-tRNA mutation-caused mitochondrial disease modeling: patients' brain in a dish S Povea-Cabello, M Villanueva-Paz… - Frontiers in …, 2021 - frontiersin.org … , MELAS (mitochondrial encephalomyopathy, lactic acidosis,…

ASTKD2 の変異は、マルチ OXPHOS 欠損症を伴うミトコンドリア病に関連

" Mutations in FASTKD2 are associated with mitochondrial disease with multi‐OXPHOS deficiency X Wei, M Du, D Li, S Wen, J Xie, Y Li, A Chen… - … Mutation, 2020 - Wiley Online Library … Alternatively, a patient with FASTKD2 mutation can sho…

ミトコンドリア病:未来への希望

" [HTML] Mitochondrial diseases: hope for the future OM Russell, GS Gorman, RN Lightowlers, DM Turnbull - Cell, 2020 - Elsevier … Several studies have shown that nuclear genetic defects are the main cause of childhoodmitochondrial disease …