Mitochondrial Dynamics and Reactive Oxygen Species Regulation

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Burt, A. L., L’Italien, G., Perlman, S. L., Rosenthal, L. S., Kuo, S., Ashizawa, T., Zesiewicz, T., Dietiker, C., Opal, P., Duquette, A., Wilmot, G. R., Shakkottai, V. G., Gomez, C. M., Srinivasan, S. R., Paulson, H., Geschwind, M. D., Worley, S., Onyike, C. U., Billnitzer, A., … Schmahmann, J. D. (2025). Spinocerebellar Ataxia Progression Measured with the Patient‐Reported Outcome Measure of Ataxia. Movement Disorders. Portico. https://doi.org/10.1002/mds.30158
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Mandel, H., Yoo, Y. J., Allen, A. J., Abedian, S., Verzani, Z., Karlson, E. W., Kleinman, L. C., Mudumbi, P. C., Oliveira, C. R., Muszynski, J. A., Gross, R. S., Carton, T. W., Kim, C., Taylor, E., Park, H., Divers, J., Kelly, J. D., Arnold, J., Geary, C. R., … Moffitt, R. A. (2025). Long-COVID incidence proportion in adults and children between 2020 and 2024. Clinical Infectious Diseases. https://doi.org/10.1093/cid/ciaf046
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Larrea, D., Tamucci, K. A., Kabra, K., Velasco, K. R., Yun, T. D., Pera, M., Montesinos, J., Agrawal, R. R., Paradas, C., Smerdon, J. W., Lowry, E. R., Stepanova, A., Yoval-Sanchez, B., Galkin, A., Wichterle, H., & Area-Gomez, E. (2025). Altered mitochondria-associated ER membrane (MAM) function shifts mitochondrial metabolism in amyotrophic lateral sclerosis (ALS). Nature Communications, 16(1). https://doi.org/10.1038/s41467-024-51578-1
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Zhou, W., Karan, K. R., Gu, W., Klein, H., Sturm, G., De Jager, P. L., Bennett, D. A., Hirano, M., Picard, M., & Mills, R. E. (2024). Nuclear mitochondrial DNA insertions are prevalent in the human brain and accumulate over time in fibroblasts. Alzheimer’s & Dementia, 20(S1). Portico. https://doi.org/10.1002/alz.085457
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Fish, L. A., Telpoukhovskaia, M., Algoo, J., Hadad, N., Gurdon, B., Dai, M., Ouellette, A. R., Neuner, S. M., Dunn, A. R., Willcox, J. A. L., Wu, Y., Dumitrescu, L. C., Bellur, O., Zhang, J., O’Connell, K. M., Dammer, E. B., Seyfried, N. T., Muzumdar, S., Gillis, J., … Kaczorowski, C. C. (2024). A cognitive resilience gene expression signature in excitatory intratelencephalic cortical neurons. Alzheimer’s & Dementia, 20(S8). Portico. https://doi.org/10.1002/alz.095063
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Qiao, M. N., Rookyard, A. N., Das, L. N., Zerlin‐Esteves, M., Reyes‐Dumeyer, D., Lee, A. J., Lantigua, R. A., Medrano, M., Mejia, D. R., Honig, L. S., Brown, L. M., Mayeux, R., & Vardarajan, B. N. (2024). Association of CSF Proteome with CSF P‐tau181 levels and other biomarkers of Alzheimer’s Disease. Alzheimer’s & Dementia, 20(S2). Portico. https://doi.org/10.1002/alz.091398
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Luquez, T., Sreenivas, D., Bennett, D. A., De Jager, P. L., & Menon, V. (2024). Cell type‐specific signatures of resilience to cognitive decline in the presence of brain pathologies. Alzheimer’s & Dementia, 20(S1). Portico. https://doi.org/10.1002/alz.088929
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Damuka, N., Gollepalli, K. K., Krizan, I., Bhoopal, B., Miller, M., Deep, O., Bashetti, N., Kumar, J. S., Orr, M. E., Macauley, S. L., Whitlow, C. T., Mintz, A., Lockhart, S. N., Craft, S., & Sai, K. K. S. (2024). Exploring Microtubule Dynamics in Alzheimer’s Disease: Longitudinal Assessment Using [11C]MPC‐6827 PET Imaging in APP/PS1 and PS301S Mouse Models. Alzheimer’s & Dementia, 20(S2). Portico. https://doi.org/10.1002/alz.090993
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Karaa, A., Bertini, E., Carelli, V., Cohen, B., Ennes, G. M., Falk, M. J., Goldstein, A., Gorman, G., Haas, R., Hirano, M., Klopstock, T., Koenig, M. K., Kornblum, C., Lamperti, C., Lehman, A., Longo, N., Molnar, M. J., Parikh, S., Phan, H., Pitceathly, R. D. S., … MMPOWER-3 Trial Investigators (2024). Genotype-specific effects of elamipretide in patients with primary mitochondrial myopathy: a post hoc analysis of the MMPOWER-3 trial. Orphanet journal of rare diseases, 19(1), 431. https://doi.org/10.1186/s13023-024-03421-5

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Blue, E. E., Huang, S. J., Khan, A., Golden-Grant, K., Boyd, B., Rosenthal, E. A., Gillentine, M. A., Fleming, L. R., Adams, D. R., Wolfe, L., Allworth, A., Bamshad, M. J., Caruana, N. J., Chanprasert, S., Chen, J., Dargie, N., Doherty, D., Friederich, M. W., Hisama, F. M., … Glass, I. A. (2024). Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts. Rare, 2, 100040. https://doi.org/10.1016/j.rare.2024.100040
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Hainsworth, A. H., Blackburn, T. P., Bradshaw, E. M., Elahi, F. M., Gorelick, P. B., Isaacs, J. D., Wallin, A., & Williams, S. C. (2024). The promise of molecular science in brain health. What breakthroughs are anticipated in the next 20 years? Cerebral Circulation - Cognition and Behavior, 7, 100364. https://doi.org/10.1016/j.cccb.2024.100364
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Hidalgo‐Gutierrez, A., Shintaku, J., Ramon, J., Barriocanal‐Casado, E., Pesini, A., Saneto, R. P., Garrabou, G., Milisenda, J. C., Matas‐Garcia, A., Gort, L., Ugarteburu, O., Gu, Y., Koganti, L., Wang, T., Tadesse, S., Meneri, M., Sciacco, M., Wang, S., Tanji, K., … Hirano, M. (2024). Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease. Annals of Neurology, 96(6), 1209–1224. Portico. https://doi.org/10.1002/ana.27071
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Tomasello, D. L., Barrasa, M. I., Mankus, D., Alarcon, K. I., Lytton-Jean, A. K. R., Liu, X. S., & Jaenisch, R. (2024). Mitochondrial dysfunction and increased reactive oxygen species production in MECP2 mutant astrocytes and their impact on neurons. Scientific Reports, 14(1). https://doi.org/10.1038/s41598-024-71040-y
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Chen, Q., Aguirre, L., Liang, G., Zhao, H., Dong, T., Borrego, F., de Rojas, I., Hu, Q., Reyes, C., Su, L.-Y., Zhang, B., Lechleiter, J. D., Göring, H. H. H., De Jager, P. L., Kleinman, J. E., Hyde, T. M., Li, P. P., Ruiz, A., Weinberger, D. R., … Ma, L. (2024). Identification of a specific APOE transcript and functional elements associated with Alzheimer’s disease. Molecular Neurodegeneration, 19(1). https://doi.org/10.1186/s13024-024-00751-7
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Zhou, W., Karan, K. R., Gu, W., Klein, H.-U., Sturm, G., De Jager, P. L., Bennett, D. A., Hirano, M., Picard, M., & Mills, R. E. (2024). Somatic nuclear mitochondrial DNA insertions are prevalent in the human brain and accumulate over time in fibroblasts. PLOS Biology, 22(8), e3002723. https://doi.org/10.1371/journal.pbio.3002723
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Paryani, F., Kwon, J.-S., Ng, C. W., Jakubiak, K., Madden, N., Ofori, K., Tang, A., Lu, H., Xia, S., Li, J., Mahajan, A., Davidson, S. M., Basile, A. O., McHugh, C., Vonsattel, J. P., Hickman, R., Zody, M. C., Housman, D. E., Goldman, J. E., … Al-Dalahmah, O. (2024). Multi-omic analysis of Huntington’s disease reveals a compensatory astrocyte state. Nature Communications, 15(1). https://doi.org/10.1038/s41467-024-50626-0
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Pannkuk, E. L., Laiakis, E. C., Garty, G., Bansal, S., Jayatilake, M. M., Tan, Y., Ponnaiya, B., Wu, X., Amundson, S. A., Brenner, D. J., & Fornace, A. J. (2024). Impact of Partial Body Shielding from Very High Dose Rates on Untargeted Metabolomics in Biodosimetry. ACS Omega, 9(32), 35182–35196. https://doi.org/10.1021/acsomega.4c05688
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Damuka, N., Irmen, R. E., Krizan, I., Miller, M., Gollapelli, K. K., Bhoopal, B., Deep, O., Bansode, A., Lockhart, S. N., Orr, M. E., Jadiya, P., Bashetti, N., Kumar, J. V. S., Mintz, A., Whitlow, C. T., Craft, S., Macauley, S. L., & Solingapuram Sai, K. K. (2024). Exploring microtubule dynamics in Alzheimer’s disease: Longitudinal assessment using [11C]MPC‐6827 PET imaging in rodent models of Alzheimer’s‐related pathology. Alzheimer’s & Dementia. Portico. https://doi.org/10.1002/alz.14083
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Kumar, A., Larrea, D., Pero, M. E., Infante, P., Conenna, M., Shin, G. J., Van Elias, V., Grueber, W. B., Di Marcotullio, L., Area-Gomez, E., & Bartolini, F. (2024). MFN2 coordinates mitochondria motility with α-tubulin acetylation and this regulation is disrupted in CMT2A. IScience, 27(6), 109994. https://doi.org/10.1016/j.isci.2024.109994
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Trumpff, C., Monzel, A. S., Sandi, C., Menon, V., Klein, H.-U., Fujita, M., Lee, A., Petyuk, V. A., Hurst, C., Duong, D. M., Seyfried, N. T., Wingo, A. P., Wingo, T. S., Wang, Y., Thambisetty, M., Ferrucci, L., Bennett, D. A., De Jager, P. L., & Picard, M. (2024). Psychosocial experiences are associated with human brain mitochondrial biology. Proceedings of the National Academy of Sciences, 121(27). https://doi.org/10.1073/pnas.2317673121
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Morcillo, P., Kabra, K., Velasco, K., Cordero, H., Jennings, S., Yun, T. D., Larrea, D., Akman, H. O., & Schon, E. A. (2024). Aberrant ER-mitochondria communication is a common pathomechanism in mitochondrial disease. Cell Death & Disease, 15(6). https://doi.org/10.1038/s41419-024-06781-9
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Corral-Sarasa, J., Martínez-Gálvez, J. M., González-García, P., Wendling, O., Jiménez-Sánchez, L., López-Herrador, S., Quinzii, C. M., Díaz-Casado, M. E., & López, L. C. (2024). 4-Hydroxybenzoic acid rescues multisystemic disease and perinatal lethality in a mouse model of mitochondrial disease. Cell Reports, 43(5), 114148. https://doi.org/10.1016/j.celrep.2024.114148
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Nguyen, T. T. T., Torrini, C., Shang, E., Shu, C., Mun, J.-Y., Gao, Q., Humala, N., Akman, H. O., Zhang, G., Westhoff, M.-A., Karpel-Massler, G., Bruce, J. N., Canoll, P., & Siegelin, M. D. (2024). OGDH and Bcl-xL loss causes synthetic lethality in glioblastoma. JCI Insight. https://doi.org/10.1172/jci.insight.172565
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Griffiths, K. K., Wang, A., Jonas, E. A., & Levy, R. J. (2024). Sulfide quinone oxidoreductase contributes to voltage sensing of the mitochondrial permeability transition pore. The FASEB Journal, 38(4). Portico. https://doi.org/10.1096/fj.202301280r
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Vega-Vásquez, T., Langgartner, D., Wang, J. Y., Reber, S. O., Picard, M., & Basualto-Alarcón, C. (2024). Mitochondrial morphology in the mouse adrenal cortex: Influence of chronic psychosocial stress. Psychoneuroendocrinology, 160, 106683. https://doi.org/10.1016/j.psyneuen.2023.106683
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Bartosch, A. M. W., Youth, E. H. H., Hansen, S., Wu, Y., Buchanan, H. M., Kaufman, M. E., Xiao, H., Koo, S. Y., Ashok, A., Sivakumar, S., Soni, R. K., Dumitrescu, L. C., Lam, T. G., Ropri, A. S., Lee, A. J., Klein, H.-U., Vardarajan, B. N., Bennett, D. A., Young-Pearse, T. L., … Teich, A. F. (2023). ZCCHC17 modulates neuronal RNA splicing and supports cognitive resilience in Alzheimer’s disease. The Journal of Neuroscience, JN-RM-2324-22. https://doi.org/10.1523/jneurosci.2324-22.2023
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Blalock, Z. N., Wu, G. W. Y., Lindqvist, D., Trumpff, C., Flory, J. D., Lin, J., Reus, V. I., Rampersaud, R., Hammamieh, R., Gautam, A., Ressler, K. J., Yang, R., Muhie, S., Daigle, B. J., Bierer, L. M., Hood, L., Wang, K., Lee, I., … Dean, K. R. (2024). Circulating cell-free mitochondrial DNA levels and glucocorticoid sensitivity in a cohort of male veterans with and without combat-related PTSD. Translational Psychiatry, 14(1). https://doi.org/10.1038/s41398-023-02721-x
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Wang, L., Rivas, R., Wilson, A., Park, Y. M., Walls, S., Yu, T., & Miller, A. C. (2023). Dose-Dependent Effects of Radiation on Mitochondrial Morphology and Clonogenic Cell Survival in Human Microvascular Endothelial Cells. Cells, 13(1), 39. https://doi.org/10.3390/cells13010039
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Levy, A. M., Ganapathi, M., Chung, W. K., & Tümer, Z. (2023). A deep intronic DLG4 variant resulting in DLG4‐related synaptopathy. Clinical Genetics, 105(1), 77–80. Portico. https://doi.org/10.1111/cge.14411
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Chang, Y.-H., Kang, E. Y.-C., Liu, L., Jenny, L. A., Khang, R., Seo, G. H., Lee, H., Chen, K.-J., Wu, W.-C., Hsiao, M.-C., & Wang, N.-K. (2023). Maternal mosaicism in SSBP1 causing optic atrophy with retinal degeneration: implications for genetic counseling. Orphanet Journal of Rare Diseases, 18(1). https://doi.org/10.1186/s13023-023-02748-9
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Shamanskiy, V., Mikhailova, A. A., Tretiakov, E. O., Ushakova, K., Mikhailova, A. G., Oreshkov, S., Knorre, D. A., Ree, N., Overdevest, J. B., Lukowski, S. W., Gostimskaya, I., Yurov, V., Liou, C.-W., Lin, T.-K., Kunz, W. S., Reymond, A., Mazunin, I., Bazykin, G. A., Fellay, J., … Popadin, K. (2023). Secondary structure of the human mitochondrial genome affects formation of deletions. BMC Biology, 21(1). https://doi.org/10.1186/s12915-023-01606-1
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Thompson, J. L. P., Karaa, A., Pham, H., Yeske, P., Krischer, J., Xiao, Y., Long, Y., Kramer, A., Dimmock, D., Holbert, A., Gorski, C., Engelstad, K. M., Buchsbaum, R., Rosales, X. Q., & Hirano, M. (2023). The evolution of the mitochondrial disease diagnostic odyssey. Orphanet Journal of Rare Diseases, 18(1). https://doi.org/10.1186/s13023-023-02754-x
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Sturm, G., Karan, K. R., Monzel, A. S., Santhanam, B., Taivassalo, T., Bris, C., Ware, S. A., Cross, M., Towheed, A., Higgins-Chen, A., McManus, M. J., Cardenas, A., Lin, J., Epel, E. S., Rahman, S., Vissing, J., Grassi, B., Levine, M., Horvath, S., … Picard, M. (2023). OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases. Communications Biology, 6(1). https://doi.org/10.1038/s42003-022-04303-x
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Arnold, M., Buyukozkan, M., Doraiswamy, P. M., Wu, T., Nho, K., Gudnason, V., Launer, L. J. J., Wang‐Sattler, R., Adamski, J., De Jager, P. L., Ertekin‐Taner, N., Bennett, D. A. A., Saykin, A. J., Peters, A., Suhre, K., Kaddurah‐Daouk, R. F., Kastenmuller, G., & Krumsiek, J. (2023). Individual bioenergetic capacity as a potential source of resilience to Alzheimer’s disease. Alzheimer’s & Dementia, 19(S12). Portico. https://doi.org/10.1002/alz.072776
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Rosenberg, A. M., Saggar, M., Monzel, A. S., Devine, J., Rogu, P., Limoges, A., Junker, A., Sandi, C., Mosharov, E. V., Dumitriu, D., Anacker, C., & Picard, M. (2023). Brain mitochondrial diversity and network organization predict anxiety-like behavior in male mice. Nature Communications, 14(1). https://doi.org/10.1038/s41467-023-39941-0
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Murari, A., Rhooms, S.-K., Vimal, D., Hossain, K. F. B., Saini, S., Villanueva, M., Schlame, M., & Owusu-Ansah, E. (2023). Phospholipids can regulate complex I assembly independent of their role in maintaining mitochondrial membrane integrity. Cell Reports, 42(8), 112846. https://doi.org/10.1016/j.celrep.2023.112846
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Fernandez Garcia, E., Paudel, U., Noji, M. C., Bowman, C. E., Rustgi, A. K., Pitarresi, J. R., Wellen, K. E., Arany, Z., Weissenrieder, J. S., & Foskett, J. K. (2023). The mitochondrial Ca2+ channel MCU is critical for tumor growth by supporting cell cycle progression and proliferation. Frontiers in Cell and Developmental Biology, 11. https://doi.org/10.3389/fcell.2023.1082213
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Agrawal, R. R., Larrea, D., Xu, Y., Shi, L., Zirpoli, H., Cummins, L. G., Emmanuele, V., Song, D., Yun, T. D., Macaluso, F. P., Min, W., Kernie, S. G., Deckelbaum, R. J., & Area-Gomez, E. (2022). Alzheimer’s-Associated Upregulation of Mitochondria-Associated ER Membranes After Traumatic Brain Injury. Cellular and Molecular Neurobiology, 43(5), 2219–2241. https://doi.org/10.1007/s10571-022-01299-0
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Yang, E. J.-N., Boldogh, I. R., Ji, H., Pon, L., & Swayne, T. C. (2023). Imaging of mtHyPer7, a Ratiometric Biosensor for Mitochondrial Peroxide, in Living Yeast Cells. Journal of Visualized Experiments, 196. https://doi.org/10.3791/65428
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Lee, A. J., Klein, H., Schneider, J. A., Bennett, D. A., De Jager, P. L., Narzisi, G., Zody, M., & Vardarajan, B. N. (2023). Association of short tandem repeats with neuropathological features in late‐onset of Alzheimer’s disease brains. Alzheimer’s & Dementia, 19(S1). Portico. https://doi.org/10.1002/alz.066552
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Menale, C., Trinchese, G., Aiello, I., Scalia, G., Dentice, M., Mollica, M. P., Yoon, N. A., & Diano, S. (2023). Nutrient-Dependent Mitochondrial Fission Enhances Osteoblast Function. Nutrients, 15(9), 2222. https://doi.org/10.3390/nu15092222
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Shang, E., Nguyen, T. T. T., Westhoff, M.-A., Karpel-Massler, G., & Siegelin, M. D. (2023). Targeting cellular respiration as a therapeutic strategy in glioblastoma. Oncotarget, 14(1), 419–425. https://doi.org/10.18632/oncotarget.28424
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Monfrini, E., Pesini, A., Biella, F., Sobreira, C. F. R., Emmanuele, V., Brescia, G., Lopez, L. C., Tadesse, S., Hirano, M., Comi, G. P., Quinzii, C. M., & Di Fonzo, A. (2023). Whole-Exome Sequencing Study of Fibroblasts Derived From Patients With Cerebellar Ataxia Referred to Investigate CoQ10 Deficiency. Neurology Genetics, 9(2). https://doi.org/10.1212/nxg.0000000000200058
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Barbuto, S., Kuo, S.-H., Winterbottom, L., Lee, S., Stern, Y., O’Dell, M., & Stein, J. (2022). Home Aerobic Training for Cerebellar Degenerative Diseases: a Randomized Controlled Trial. The Cerebellum, 22(2), 272–281. https://doi.org/10.1007/s12311-022-01394-4
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Padavannil, A., Murari, A., Rhooms, S.-K., Owusu-Ansah, E., & Letts, J. A. (2023). Resting mitochondrial complex I from Drosophila melanogaster adopts a helix-locked state. ELife, 12. CLOCKSS. https://doi.org/10.7554/elife.84415
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Hossain, K. F. B., Murari, A., Mishra, B., & Owusu-Ansah, E. (2022). The membrane domain of respiratory complex I accumulates during muscle aging in Drosophila melanogaster. Scientific Reports, 12(1). https://doi.org/10.1038/s41598-022-26414-5
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