The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Mitochondrial division and fusion in metabolism
Open accessAbstract
Mitochondria govern many metabolic processes. In addition, mitochondria sense the status of metabolism and change their functions to regulate energy production, cell death, and thermogenesis. Recent studies have revealed that mitochondrial structural remodeling through division and fusion is critical to the organelle’s function. It has also become clear that abnormalities in mitochondrial division and fusion are linked to the pathophysiology of metabolic diseases such as diabetes and obesity. Here, we discuss the current understanding of the mechanisms of mitochondrial dynamics and their role in cellular and organismal metabolism.
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Citations
Cites
Mitochondrial Fission, Fusion, and Stress
Youle, R. J., & van der Bliek, A. M. (2012) · Science · doi:10.1126/science.1219855 · Cited by 3,674 · cited 1×
“com Mitochondrial dynamics refer to the perpetual process of fusion, division, movement, and morphological changes which take place in response to the ever-changing physiological demands of cells [13,14].”
Fission and selective fusion govern mitochondrial segregation and elimination by autophagy
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Mitochondrial form and function
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During autophagy mitochondria elongate, are spared from degradation and sustain cell viability
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OPA1 Controls Apoptotic Cristae Remodeling Independently from Mitochondrial Fusion
Frezza, C., Cipolat, S., Martins de Brito, O., Micaroni, M., Beznoussenko, G. V., Rudka, T., Bartoli, D., Polishuck, R. S., Danial, N. N., De Strooper, B., et al. (2006) · Cell · doi:10.1016/j.cell.2006.06.025 · Cited by 1,673
Proteasome and p97 mediate mitophagy and degradation of mitofusins induced by Parkin
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Mitochondrial Dynamics in the Regulation of Nutrient Utilization and Energy Expenditure
Liesa, M., & Shirihai, O. S. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.03.002 · Cited by 1,341
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Fusion and fission: interlinked processes critical for mitochondrial health
Chan, D. C. (2012) · Annual Review of Genetics · doi:10.1146/annurev-genet-110410-132529 · Cited by 1,196 · cited 2×
“Defects in the core components of these systems, three dynamin-related GTPases, give rise to several disease conditions, including neonatal death with severe neural defects (defects in outer membrane protein Drp1, which mediates division), Charcot-Marie-Tooth neuropathy type 2A, a neurodegenerative disease of peripher…”
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Cited by
Bhatti, J. S., Bhatti, G. K., & Reddy, P. H. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2016.11.010 · Cited by 1,655
Self-citationEelen, G., de Zeeuw, P., Treps, L., Harjes, U., Wong, B. W., & Carmeliet, P. (2018) · Physiological Reviews · doi:10.1152/physrev.00001.2017 · Cited by 572
Imbalanced OPA1 processing and mitochondrial fragmentation cause heart failure in mice
Wai, T., García-Prieto, J., Baker, M. J., Merkwirth, C., Benit, P., Rustin, P., Rupérez, F. J., Barbas, C., Ibañez, B., & Langer, T. (2015) · Science · doi:10.1126/science.aad0116 · Cited by 551
Evaluating Cell Metabolism Through Autofluorescence Imaging of NAD(P)H and FAD
Kolenc, O. I., & Quinn, K. P. (2019) · Antioxidants & Redox Signaling · doi:10.1089/ars.2017.7451 · Cited by 365
Mitochondrial fusion/fission dynamics in neurodegeneration and neuronal plasticity
Bertholet, A. M., Delerue, T., Millet, A. M., Moulis, M. F., David, C., Daloyau, M., Arnauné-Pelloquin, L., Davezac, N., Mils, V., Miquel, M. C., et al. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.10.011 · Cited by 363
Metadata
- Authors
- Roy, M., Reddy, P. H., Iijima, M., & Sesaki, H.
- Venue
- Current Opinion in Cell Biology
- Publisher
- Elsevier BV
- Published
- 2015-04
- Volume
- 33
- Pages
- 111-118
- ISSN
- 0955-0674 (ISSN-L)
- OpenAlex
- W2073902042
- Cited by
- 207
- References
- 27
- FWCI
- 1.93
- Type
- journal article
- Language
- en
- Open access
- green
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