» Articles » PMID: 20725092

Mitochondrial Shape Changes: Orchestrating Cell Pathophysiology

Overview
Journal EMBO Rep
Specialty Molecular Biology
Date 2010 Aug 21
PMID 20725092
Citations 137
Authors
Affiliations
Soon will be listed here.
Abstract

Mitochondria are highly dynamic organelles, the location, size and distribution of which are controlled by a family of proteins that modulate mitochondrial fusion and fission. Recent evidence indicates that mitochondrial morphology is crucial for cell physiology, as changes in mitochondrial shape have been linked to neurodegeneration, calcium signalling, lifespan and cell death. Because immune cells contain few mitochondria, these organelles have been considered to have only a marginal role in this physiological context-which is conversely well characterized from the point of view of signalling. Nevertheless, accumulating evidence shows that mitochondrial dynamics have an impact on the migration and activation of immune cells and on the innate immune response. Here, we discuss the roles of mitochondrial dynamics in cell pathophysiology and consider how studying dynamics in the context of the immune system could increase our knowledge about the role of dynamics in key signalling cascades.

Citing Articles

Hypoxia-Induced Metabolic and Functional Changes in Oral CSCs: Implications for Stemness and Viability Modulation Through BNIP3-Driven Mitophagy.

Li X, Chaouhan H, Yu S, Wang I, Yu T, Chuang Y J Cell Mol Med. 2025; 29(3):e70400.

PMID: 39945227 PMC: 11822456. DOI: 10.1111/jcmm.70400.


Nutrient status alters developmental fates via a switch in mitochondrial homeodynamics.

Zhang J, Liu S, Li Y, Xu G, Deng H, King-Jones K Nat Commun. 2025; 16(1):1258.

PMID: 39893174 PMC: 11787341. DOI: 10.1038/s41467-025-56528-z.


A pathogenic mutation in the ALS/FTD gene VCP induces mitochondrial hypermetabolism by modulating the permeability transition pore.

Vanderhaeghe S, Prerad J, Tharkeshwar A, Goethals E, Vints K, Beckers J Acta Neuropathol Commun. 2024; 12(1):161.

PMID: 39390590 PMC: 11465669. DOI: 10.1186/s40478-024-01866-0.


GTPBP8 modulates mitochondrial fission through a Drp1-dependent process.

He X, Wang L, Tsang H, Liu X, Yang X, Pu S J Cell Sci. 2024; 137(8).

PMID: 38587461 PMC: 11112121. DOI: 10.1242/jcs.261612.


Autologous non-invasively derived stem cells mitochondria transfer shows therapeutic advantages in human embryo quality rescue.

Jiang Z, Shi C, Han H, Fu M, Zhu H, Han T Biol Res. 2023; 56(1):60.

PMID: 37978575 PMC: 10657142. DOI: 10.1186/s40659-023-00470-1.


References
1.
Bellot G, Garcia-Medina R, Gounon P, Chiche J, Roux D, Pouyssegur J . Hypoxia-induced autophagy is mediated through hypoxia-inducible factor induction of BNIP3 and BNIP3L via their BH3 domains. Mol Cell Biol. 2009; 29(10):2570-81. PMC: 2682037. DOI: 10.1128/MCB.00166-09. View

2.
Dimmer K, Navoni F, Casarin A, Trevisson E, Endele S, Winterpacht A . LETM1, deleted in Wolf-Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability. Hum Mol Genet. 2007; 17(2):201-14. DOI: 10.1093/hmg/ddm297. View

3.
Glick D, Barth S, Macleod K . Autophagy: cellular and molecular mechanisms. J Pathol. 2010; 221(1):3-12. PMC: 2990190. DOI: 10.1002/path.2697. View

4.
Novak I, Kirkin V, McEwan D, Zhang J, Wild P, Rozenknop A . Nix is a selective autophagy receptor for mitochondrial clearance. EMBO Rep. 2009; 11(1):45-51. PMC: 2816619. DOI: 10.1038/embor.2009.256. View

5.
Harder Z, Zunino R, McBride H . Sumo1 conjugates mitochondrial substrates and participates in mitochondrial fission. Curr Biol. 2004; 14(4):340-5. DOI: 10.1016/j.cub.2004.02.004. View