The constriction and scission machineries involved in mitochondrial fission

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ER Tubules Mark Sites of Mitochondrial Division

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Mitochondrial Dynamics Controls T Cell Fate through Metabolic Programming

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Mitochondria in Apoptosis: Bcl-2 Family Members and Mitochondrial Dynamics

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Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission

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Tubular network formation protects mitochondria from autophagosomal degradation during nutrient starvation

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Metabolic regulation of mitochondrial dynamics

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Reversible association with motor proteins (RAMP): A streptavidin-based method to manipulate organelle positioning

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Phosphorylation of Dynamin-Related Protein 1 (DRP1) Regulates Mitochondrial Dynamics and Skeletal Muscle Wasting in Cancer Cachexia

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Comprehensive Analysis of Mitochondrial Dynamics Alterations in Heart Diseases

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Neurotrophins induce fission of mitochondria along embryonic sensory axons

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Loss of Fis1 impairs proteostasis during skeletal muscle aging in Drosophila

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Mitochondrial dynamics in neurological diseases: a narrative review

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How neurons maintain their axons long-term: an integrated view of axon biology and pathology

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Role of Flavonoids in Modulation of Mitochondria Dynamics during Oxidative Stress

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Novel findings on ultrastructural protection of skeletal muscle fibers during hibernation of Daurian ground squirrels: Mitochondria, nuclei, cytoskeleton, glycogen

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The anti-viral dynamin family member MxB participates in mitochondrial integrity

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Mitochondrial dynamics in the neonatal brain – a potential target following injury?

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NovelDNM1Lvariants impair mitochondrial dynamics through divergent mechanisms

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Role of apolipoprotein E in electronegative low-density lipoprotein-induced mitochondrial dysfunction in cardiomyocytes

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Novel ultrastructural findings on cardiac mitochondria of huddling Brandt's voles in mild cold environment

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Inactivation of cardiolipin synthase triggers changes in mitochondrial morphology

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Role of Mitochondrial Dynamics in Cocaine’s Neurotoxicity

Wen, S., Aki, T., Funakoshi, T., Unuma, K., & Uemura, K. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105418 · Cited by 25

CypD deficiency confers neuroprotection against mitochondrial abnormality caused by lead in SH-SY5Y cell

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Unraveling mitochondrial dysfunction: comprehensive perspectives on its impact on neurodegenerative diseases

Yusoff, A. A. M., & Khair, S. Z. N. M. (2024) · Reviews in the Neurosciences · doi:10.1515/revneuro-2024-0080 · Cited by 23

Novel insight into mitochondrial dynamin-related protein-1 as a new chemo-sensitizing target in resistant cancer cells

Alkafaas, S. S., Obeid, O. K., Radwan, M. A., Elsalahaty, M. I., Elkafas, S. S., Hafez, W., Janković, N., & Hessien, M. (2024) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2024.107574 · Cited by 21

Plant Mitophagy in Comparison to Mammals: What Is Still Missing?

Ren, K., Feng, L., Sun, S., & Zhuang, X. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22031236 · Cited by 22

USP15 regulates p66Shc stability associated with Drp1 activation in liver ischemia/reperfusion

Tian, X., Zhao, Y., Yang, Z., Lu, Q., Zhou, L., & Zheng, S. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05277-8 · Cited by 20

Targeting mitochondrial dysfunctions in pancreatic cancer evokes new therapeutic opportunities

Sarwar, A., Zhu, M., Su, Q., Zhu, Z., Yang, T., Chen, Y., Peng, X., & Zhang, Y. (2022) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2022.103858 · Cited by 20

Drp1: Focus on Diseases Triggered by the Mitochondrial Pathway

Sun, F., Fang, M., Zhang, H., Song, Q., Li, S., Li, Y., Jiang, S., & Yang, L. (2024) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-024-01245-5 · Cited by 21

The Shape of Mitochondrial Dysfunction in Down Syndrome

Zamponi, E., & Helguera, P. R. (2019) · Developmental Neurobiology · doi:10.1002/dneu.22673 · Cited by 20

Regulation of mitochondrial fission by GIPC-mediated Drp1 retrograde transport

Ramonett, A., Kwak, E.-A., Ahmed, T., Flores, P. C., Ortiz, H. R., Lee, Y. S., Vanderah, T. W., Largent-Milnes, T., Kashatus, D. F., Langlais, P. R., et al. (2021) · Molecular Biology of the Cell · doi:10.1091/mbc.e21-06-0286 · Cited by 19

Multifaceted role of dynamin-related protein 1 in cardiovascular disease: From mitochondrial fission to therapeutic interventions

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Miro1 functions as an inhibitory regulator of MFN at elevated mitochondrial Ca2+ levels

Fatiga, F. F., Wang, L., Hsu, T., Capuno, J. I., & Fu, C. (2021) · Journal of Cellular Biochemistry · doi:10.1002/jcb.30138 · Cited by 20

Targeting mitochondrial structure and dynamics for therapeutic intervention in cancer

Iwata, W., Haggerty, N., Sesaki, H., & Iijima, M. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003453 · Cited by 19

Fission Impossible (?)—New Insights into Disorders of Peroxisome Dynamics

Carmichael, R. E., Islinger, M., & Schrader, M. (2022) · Cells · doi:10.3390/cells11121922 · Cited by 21

Inhibition of Drp1 Sensitizes Cancer Cells to Cisplatin-Induced Apoptosis through Transcriptional Inhibition of c-FLIP Expression

Woo, S. M., Min, K., & Kwon, T. K. (2020) · Molecules · doi:10.3390/molecules25245793 · Cited by 18

Sestrin2 and mitochondrial quality control: Potential impact in myogenic differentiation

Piochi, L. F., Machado, I. F., Palmeira, C. M., & Rolo, A. P. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101309 · Cited by 21

A Molecular Perspective on Mitochondrial Membrane Fusion: From the Key Players to Oligomerization and Tethering of Mitofusin

Vecchis, D. D., Brandner, A. F., Baaden, M., Cohen, M. M., & Taly, A. (2019) · The Journal of Membrane Biology · doi:10.1007/s00232-019-00089-y · Cited by 20

Region-specific mitophagy in nucleus pulposus, annulus fibrosus, and cartilage endplate of intervertebral disc degeneration: mechanisms and therapeutic strategies

Feng, C., Hu, Z., Zhao, M., Leng, C., Li, G., Yang, F., & Fan, X. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1579507 · Cited by 22

Aldehyde dehydrogenase 2 preserves mitochondrial morphology and attenuates hypoxia/reoxygenation-induced cardiomyocyte injury

Zhang, R. (2020) · World Journal of Emergency Medicine · doi:10.5847/wjem.j.1920-8642.2020.04.007 · Cited by 16

The Role of Mitochondrial Dynamin in Stroke

Li, C., Chen, C., Qin, H., Ao, C., Chen, J., Tan, J., & Zeng, L. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/2504798 · Cited by 19

Biological properties of the BCL-2 family protein BCL-RAMBO, which regulates apoptosis, mitochondrial fragmentation, and mitophagy

Kataoka, T. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1065702 · Cited by 17

NSD2 modulates Drp1-mediated mitochondrial fission in chronic renal allograft interstitial fibrosis by methylating STAT1

Zhang, J., Xie, W., Ni, B., Li, Z., Feng, D., Zhang, Y., Han, Q., Zhou, H., Gu, M., & Tan, R. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2023.107051 · Cited by 17

Dynamic regulation of subcellular mitochondrial position for localized metabolite levels

Alshaabi, H., Heininger, M., & Cunniff, B. (2019) · The Journal of Biochemistry · doi:10.1093/jb/mvz058 · Cited by 18

Divide et Impera: Drp1-mediated Mitochondrial Fission in Glioma Malignancy.

Eugenio-Pérez, D., Briones‐Herrera, A., Martínez‐Klimova, E., & Pedraza‐Chaverrí, J. (2019) · Europe PMC (PubMed Central) · Cited by 17

Mitochondrial connections with immune system in Zebrafish

do Amaral, M. A., Paredes, L. C., Padovani, B. N., Mendonça-Gomes, J. M., Montes, L. F., Câmara, N. O. S., & Morales, C. (2021) · Fish and Shellfish Immunology Reports · doi:10.1016/j.fsirep.2021.100019 · Cited by 17

Approaches to Mitigate Mitochondrial Dysfunction in Sensorineural Hearing Loss

Okur, M. N., & Djalilian, H. R. (2022) · Annals of Biomedical Engineering · doi:10.1007/s10439-022-03103-y · Cited by 18

Genetic Neuropathy Due to Impairments in Mitochondrial Dynamics

Sharma, G., Pfeffer, G., & Shutt, T. E. (2021) · Biology · doi:10.3390/biology10040268 · Cited by 18

Mitochondrial transport, partitioning, and quality control at the heart of cell proliferation and fate acquisition

Sharma, R. K., Chafik, A., & Bertolin, G. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00256.2021 · Cited by 16

Mitochondria in Cancer Stem Cells: From an Innocent Bystander to a Central Player in Therapy Resistance

Garimella, S. V., Gampa, S. C., & Chaturvedi, P. (2023) · Stem Cells and Cloning Advances and Applications · doi:10.2147/sccaa.s417842 · Cited by 16

Proteolytic regulation of mitochondrial dynamics

Dietz, J. V., Bohovych, I., Viana, M. P., & Khalimonchuk, O. (2019) · Mitochondrion · doi:10.1016/j.mito.2019.04.008 · Cited by 15

High-fat diet exacerbates 1-Bromopropane-induced loss of dopaminergic neurons in the substantia nigra of mice through mitochondrial damage associated necroptotic pathway

Song, M., Qiang, Y., Wang, S., Shan, S., Zhang, L., Liu, C., Song, F., & Zhao, X. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.116280 · Cited by 14

Role of mitochondrial quality control in neurodegenerative disease progression

Liu, T., Sun, W., Guo, S., Yuan, Z., Zhu, M., Lu, J., Chen, T., Qu, Y., Feng, C., & Yang, T. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2025.1588645 · Cited by 16

Do You Remember Mitochondria?

Messina, F., Cecconi, F., & Rodolfo, C. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00271 · Cited by 14

Mitochondria-Shaping Proteins and Chemotherapy

Xie, L., Zhou, T., Xie, Y., Bode, A. M., & Cao, Y. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.769036 · Cited by 13

On the offense and defense: mitochondrial recovery programs amidst targeted pathogenic assault

Mahmud, S. A., Qureshi, M. A., & Pellegrino, M. W. (2021) · FEBS Journal · doi:10.1111/febs.16126 · Cited by 13

Role of GTPases in the regulation of mitochondrial dynamics in Parkinson's disease

Zhang, X., Huang, W., Fan, Y.-Y., Sun, Y. J., & Ge, X. (2019) · Experimental Cell Research · doi:10.1016/j.yexcr.2019.06.005 · Cited by 14

Axonal transport dysfunction of mitochondria in traumatic brain injury: A novel therapeutic target

Shin, S. S., Karlsson, M., Mazandi, V. M., Ranganathan, A., Hallowell, T., Delso, N., & Kilbaugh, T. J. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113311 · Cited by 13

Loss and recovery of myocardial mitochondria in mice under different tail suspension time: Apoptosis and mitochondrial fission, fusion and autophagy

Wang, Z., Wang, X. T., Chen, Y.-F., Wang, C., Chen, L., Jiang, M., Liu, X., Zhang, X., Feng, Y., & Xu, J. (2023) · Experimental Physiology · doi:10.1113/ep090518 · Cited by 11

Enhanced T cell immune activity mediated by Drp1 promotes the efficacy of PD-1 inhibitors in treating lung cancer

Ma, J., Song, J., Yi, X., Zhang, S., Sun, L., Huang, L., & Han, C. (2024) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-023-03582-5 · Cited by 13

SS‐31 does not prevent or reduce muscle atrophy 7 days after a 65 kdyne contusion spinal cord injury in young male mice

Graham, Z., DeBerry, J. J., Cardozo, C. P., & Bamman, M. M. (2022) · Physiological Reports · doi:10.14814/phy2.15266 · Cited by 10

Mitochondrial quality control in abdominal aortic aneurysm: From molecular mechanisms to therapeutic strategies

Wang, D., Jia, L., Zhao, C., Wang, H., Dai, Z., Jing, Y., Jiang, B., & Xin, S. (2023) · The FASEB Journal · doi:10.1096/fj.202202158rr · Cited by 12

Principles of mitochondrial vesicle transport

McLelland, G., & Fon, E. A. (2018) · Current Opinion in Physiology · doi:10.1016/j.cophys.2018.02.005 · Cited by 12

Plasticity in salt bridge allows fusion-competent ubiquitylation of mitofusins and Cdc48 recognition

Anton, V., Buntenbroich, I., Schuster, R., Gaedke, F., Simões, T., Altin, S., Calabrese, G., Riemer, J., Schauss, A. C., & Escobar‐Henriques, M. (2019) · Life Science Alliance · doi:10.26508/lsa.201900491 · Cited by 13

Geometric instability catalyzes mitochondrial fission

Irajizad, E., Ramachandran, R., & Agrawal, A. (2018) · Molecular Biology of the Cell · doi:10.1091/mbc.e18-01-0018 · Cited by 10

Hexokinase II dissociation alone cannot account for changes in heart mitochondrial function, morphology and sensitivity to permeability transition pore opening following ischemia

Pereira, G. C., Lee, L. J., Rawlings, N., Ouwendijk, J., Parker, J. E., Andrienko, T., Henley, J. M., & Halestrap, A. P. (2020) · PLoS ONE · doi:10.1371/journal.pone.0234653 · Cited by 11

A link between protein acetylation and mitochondrial dynamics under energy metabolism: A comprehensive overview

Gu, H., Yang, K., Wu, Q., Shen, Z., Li, X., & Sun, C. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30461 · Cited by 11

MSCs Ameliorate Hepatic IR Injury by Modulating Phenotypic Transformation of Kupffer Cells Through Drp-1 Dependent Mitochondrial Dynamics

Shang, L., Wang, M., Liu, Y., Zhu, X., & Wang, S. (2023) · Stem Cell Reviews and Reports · doi:10.1007/s12015-023-10566-6 · Cited by 11

Defining the Role of Mitochondrial Fission in Corneal Myofibroblast Differentiation

Jeon, K., Kumar, A., Wozniak, K. T., Nehrke, K. W., & Huxlin, K. R. (2022) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.63.4.2 · Cited by 12

Convergent and divergent mechanisms of peroxisomal and mitochondrial division

Subramani, S. E., Shukla, N., & Farré, J. (2023) · The Journal of Cell Biology · doi:10.1083/jcb.202304076 · Cited by 10

Drp1 regulated PINK1-dependent mitophagy protected duck follicular granulosa cells from acute heat stress injury

Yang, C., Luo, P., Yang, Y., Fu, X., Li, B., Shen, X., Xu, D., Huang, Y., Tian, Y., & Liu, W. (2023) · Poultry Science · doi:10.1016/j.psj.2023.103247 · Cited by 10

Distinct Contributions of the Peroxisome-Mitochondria Fission Machinery During Sexual Development of the Fungus Podospora anserina

Navarro-Espíndola, R., Takano‐Rojas, H., Suaste-Olmos, F., & Peraza‐Reyes, L. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00640 · Cited by 12

DRP1: shedding light on the complex nexus of mitochondrial fission and breast cancer

You, L., Wang, M., Liu, X., Song, M., Zhou, J., Feng, J., & Liu, J. (2024) · Future Oncology · doi:10.1080/14796694.2024.2447813 · Cited by 9

Balancing act: Drp1 inhibition and mitochondrial homeostasis in cardiovascular diseases

Dubey, N., Goyal, A., Parakh, N., Narang, R., Arava, S. K., Kumar, A., Yadav, M., & Yadav, H. N. (2025) · Vascular Pharmacology · doi:10.1016/j.vph.2025.107531 · Cited by 9

Cyclin-dependent Kinase 5 and Neurodegenerative Diseases

Song, M., Qiang, Y., Zhao, X., & Song, F. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04047-1 · Cited by 10

GTPBP8 modulates mitochondrial fission through a Drp1-dependent process

He, X., Wang, L., Tsang, H. Y., Liu, X., Yang, X., Pu, S., Guo, Z., Yang, C., Wu, Q., Zhou, Z., et al. (2024) · Journal of Cell Science · doi:10.1242/jcs.261612 · Cited by 9

GOLPH3 Participates in Mitochondrial Fission and Is Necessary to Sustain Bioenergetic Function in MDA-MB-231 Breast Cancer Cells

Polanco, C. M., Cavieres, V. A., Galarza, A. J., Jara, C., Torres, A. K., Cancino, J., Varas‐Godoy, M., Burgos, P. V., Tapia‐Rojas, C., & Mardones, G. A. (2024) · Cells · doi:10.3390/cells13040316 · Cited by 8

Biogenesis, inheritance, and 3D ultrastructure of the microsporidian mitosome

Hacker, C., Sendra, K. M., Keisham, P., Filipescu, T., Lucocq, J. E., Salimi, F., Ferguson, S., Bhella, D., MacNeill, S. A., Embley, T. M., et al. (2023) · Life Science Alliance · doi:10.26508/lsa.202201635 · Cited by 9

The Large GTPase Guanylate-Binding Protein-1 (GBP-1) Promotes Mitochondrial Fission in Glioblastoma

Kalb, R. C., Nyabuto, G. O., Morran, M. P., Maity, S., Justinger, J. S., Nestor‐Kalinoski, A. L., & Vestal, D. J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252011236 · Cited by 7

Dictyostelium Dynamin Superfamily GTPases Implicated in Vesicle Trafficking and Host-Pathogen Interactions

Katic, A., Hüsler, D., Letourneur, F., & Hilbi, H. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.731964 · Cited by 5

Research progress on ncRNAs regulation of mitochondrial dynamics in diabetes

Wu, Y., Lan, H., Zhang, D., Hu, Z., Zhang, J., Li, Z., Xia, P., Tang, X., Cai, X., & Yu, P. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30878 · Cited by 7

Adverse effects of 2-Methoxyestradiol on mouse oocytes during reproductive aging

Jiang, X., Xu, X., Wang, B., Song, K., Zhang, J., Chen, Y., Tian, Y., Weng, J., Liang, Y., & Ma, W. (2022) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2022.110277 · Cited by 7

MAPL loss dysregulates bile and liver metabolism in mice

Goyon, V., Besse‐Patin, A., Zunino, R., Ignatenko, O., Nguyen, M., Coyaud, É., Lee, J. M., Nguyen, B., Raught, B., & McBride, H. M. (2023) · EMBO Reports · doi:10.15252/embr.202357972 · Cited by 6

Dynamin-2 R465W mutation induces long range perturbation in highly ordered oligomeric structures

Hinostroza, F., Neely, A., Araya‐Durán, I., Marabolí, V., Canan, J., Rojas, M., Aguayo, D., Latorre, R., González-Nilo, F. D., & Cárdenas, A. M. (2020) · Scientific Reports · doi:10.1038/s41598-020-75216-0 · Cited by 7

SEPTIN9 locally activates the RhoGEF ARHGEF18 to promote early stages of mitochondrial fission

Shannon, R., Balachandran, Y., Wang, X., Boutry, M., Xie, H., Kim, P. K., & Trimble, W. S. (2025) · The Journal of Cell Biology · doi:10.1083/jcb.202406017 · Cited by 6

Mitochondrial dynamics and signaling in stem cell differentiation

Verma, R. K., Madan, S., & Rikhy, R. (2026) · Journal of Cell Science · doi:10.1242/jcs.263847 · Cited by 6

Sexually dimorphic hepatic mitochondrial adaptations to exercise: a mini-review

Kugler, B. A., Thyfault, J. P., & McCoin, C. S. (2023) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00711.2022 · Cited by 5

Mitochondrial dynamics, biogenesis, mitophagy and oxidative stress in gestational obesity: A review

Rodríguez-Córdoba, K. M., Agreda-Soto, S., Garzón, J. A. C., & Pustovrh, M. C. (2024) · Endocrine and Metabolic Science · doi:10.1016/j.endmts.2024.100205 · Cited by 7

Fatty Acids at the Crossroads of Mitochondria Dynamics in Macrophages

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