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Dynamics of mitochondria in living cells: Shape changes, dislocations, fusion, and fission of mitochondria
Abstract
Mitochondria are semi‐autonomous organelles which are endowed with the ability to change their shape (e.g., by elongation, shortening, branching, buckling, swelling) and their location inside a living cell. In addition they may fuse or divide. These dynamics are discussed. Dislocation of mitochondria may result from their interaction with elements of the cytoskeleton, with microtubules in particular, and from processes intrinsic to the mitochondria themselves. Morphological criteria and differences in the fate of some mitochondria argue for the presence of more than one mitochondrial population in some animal cells. Whether these reflect genetic differences remains obscure. Emphasis is laid on the methods for visualizing mitochondria in cells and following their behaviour. Fluorescence methods provide unique possibilities because of their high resolving power and because some of the mitochondria‐specific fluorochromes can be used to reveal the membrane potential. Fusion and fission often occur in short time intervals within the same group of mitochondria. At sites of fusion of two mitochondria material of the inner membrane, the matrix compartment seems to accumulate. The original arrangement of the fusion partners is maintained for some minutes. Fission is a dynamic event which, like fusion, in most cases observed in vertebrate cell cultures is not a straightforward process but rather requires several “trials” until the division finally occurs. Regarding fusion and fission hitherto unpublished phase contrast micrographs, and electron micrographs have been included. © 1994 Wiley‐Liss, Inc.
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“Mitochondrial fusion allows for greater adenosine triphosphate (ATP) production during conditions of high metabolic activity”
From Sex Differences in Traumatic Brain Injury: What We Know and What We Should Know (2019) · cites this paper as [132]
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Bereiter‐Hahn, J., Münnich, A., & Woiteneck, P. (1998) · Cell Structure and Function · doi:10.1247/csf.23.85 · Cited by 45
Self-citationMitochondrial dynamics in filamentous fungi
Westermann, B., & Prokisch, H. (2002) · Fungal Genetics and Biology · doi:10.1016/s1087-1845(02)00019-1 · Cited by 45
Sexuality of Mitochondria: Fusion, Recombination, and Plasmids
Kawano, S., Takano, H., & Kuroiwa, T. (1995) · International review of cytology · doi:10.1016/s0074-7696(08)62496-1 · Cited by 45
Mitochondrial Dynamics at Different Levels: From Cristae Dynamics to Interorganellar Cross Talk
Kondadi, A. K., & Reichert, A. S. (2024) · Annual Review of Biophysics · doi:10.1146/annurev-biophys-030822-020736 · Cited by 46
Role of Mitochondrial Dysfunctions in Neurodegenerative Disorders: Advances in Mitochondrial Biology
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Mitochondrial displacements in response to nanomechanical forces
Silberberg, Y. R., Pelling, A. E., Yakubov, G. E., Crum, W. R., Hawkes, D. J., & Horton, M. A. (2008) · Journal of Molecular Recognition · doi:10.1002/jmr.868 · Cited by 44
Mitophagy, mitochondrial dynamics and the general stress response in yeast
Müller, M., & Reichert, A. S. (2011) · Biochemical Society Transactions · doi:10.1042/bst0391514 · Cited by 43
Time representation of mitochondrial morphology and function after acute spinal cord injury
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Enantioselective cellular localisation of europium( iii ) coordination complexes
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Saks, V. A., Santos, P. D. D., Gellerich, F. N., & Diolez, P. (1998) · Molecular and Cellular Biochemistry · doi:10.1023/a:1006828106322 · Cited by 44
Cell and animal models of mtDNA biology: progress and prospects
Khan, S. M., Smigrodzki, R. M., & Swerdlow, R. H. (2006) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00224.2006 · Cited by 43
Kowald, A., Jendrach, M., Pohl, S., Bereiter‐Hahn, J., & Hammerstein, P. (2005) · Aging Cell · doi:10.1111/j.1474-9726.2005.00169.x · Cited by 43
Self-citationDiaz, G., Falchi, A. M., Gremo, F., Isola, R., & Diana, A. (2000) · FEBS Letters · doi:10.1016/s0014-5793(00)01683-5 · Cited by 43
High‐pressure freezing of epithelial cells on sapphire coverslips
Reipert, S., Fischer, I., & Wiche, G. (2003) · Journal of Microscopy · doi:10.1111/j.1365-2818.2004.01260.x · Cited by 43
Regulation of mitochondrial dynamics and neurodegenerative diseases.
Han, X.-J., Tomizawa, K., Fujimura, A., Ohmori, I., Nishiki, T., Matsushita, M., & Matsui, H. (2011) · PubMed · doi:10.18926/amo/43824 · Cited by 41
Metadata
- Authors
- Bereiter‐Hahn, J., & Vöth, M.
- Affiliations
- Goethe University Frankfurt (DE)
- Corresponding author
- Bereiter‐Hahn, J.
- Venue
- Microscopy Research and Technique
- Publisher
- Wiley
- Published
- 1994-02-15
- Volume
- 27
- Issue
- 3
- Pages
- 198-219
- ISSN
- 1059-910X (ISSN-L)
- 1097-0029
- OpenAlex
- W2060811345
- Cited by
- 900
- References
- 223
- Citations by year
- 2026: 12 · 2025: 19 · 2024: 24 · 2023: 20 · 2022: 24 · 2021: 33 · 2020: 31 · 2019: 33 · 2018: 33 · 2017: 32 · 2016: 28 · 2015: 33 · 2014: 45 · 2013: 33 · 2012: 52
- FWCI
- 1.07
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Microscopy Research and Technique (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Keywords
- mitochondrial dynamics, mitochondrial fusion, mitochondrial fission, microtubules, mitochondrial membrane potential, mitochondrial swelling, mitochondrial heterogeneity, fluorescence microscopy
- MeSH terms
- Animals, Cell Movement, Cytoskeletal Proteins, Fluorescent Dyes, HeLa Cells, Humans, Membrane Fusion, Microscopy, Fluorescence, Microtubules, Mitochondria, Xenopus, Cell Size
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