Crosstalk between mitochondrial (dys)function and mitochondrial abundance
| Autor: | Guillaume Rommelaere, Aurélia De Pauw, Anaïs Wanet, Patricia Renard, Sébastien Michel, Thierry Arnould |
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| Rok vydání: | 2012 |
| Předmět: |
DNA Replication
Transcription Genetic Physiology Clinical Biochemistry Biology Mitochondrion DNA Mitochondrial Mitochondrial Proteins Mitochondrial myopathy Stress Physiological Mitophagy Autophagy medicine Animals Homeostasis Humans Cellular Senescence Cell Biology medicine.disease Mitochondria Cell biology Gene Expression Regulation mitochondrial fusion Mitochondrial biogenesis DNAJA3 Biogenesis Molecular Chaperones Peptide Hydrolases Signal Transduction |
| Zdroj: | Journal of Cellular Physiology. 227:2297-2310 |
| ISSN: | 0021-9541 |
| Popis: | A controlled regulation of mitochondrial mass through either the production (biogenesis) or the degradation (mitochondrial quality control) of the organelle represents a crucial step for proper mitochondrial and cell function. Key steps of mitochondrial biogenesis and quality control are overviewed, with an emphasis on the role of mitochondrial chaperones and proteases that keep mitochondria fully functional, provided the mitochondrial activity impairment is not excessive. In this case, the whole organelle is degraded by mitochondrial autophagy or "mitophagy". Beside the maintenance of adequate mitochondrial abundance and functions for cell homeostasis, mitochondrial biogenesis might be enhanced, through discussed signalling pathways, in response to various physiological stimuli, like contractile activity, exposure to low temperatures, caloric restriction and stem cells differentiation. In addition, mitochondrial dysfunction might also initiate a retrograde response, enabling cell adaptation through increased mitochondrial biogenesis. Although the examples cited above suggest that the control of mitochondrial mass, through biogenesis or quality control, is beneficial to the cell/organism demands, the data generated from diverse pathologies suggest that modulations in mitochondrial abundance/functions may participate to the pathogenesis. Increased mitochondrial abundance is generally described to characterize mitochondrial myopathies as well as most cancers, and is generally accompanied by qualitative modifications of mitochondria, thereby affecting programmed cells death susceptibility. On the contrary, in ageing, obesity and type 2 diabetes, mitochondrial biogenesis and functions are generally down-regulated. The development of insulin resistance, favoured by an impaired mitochondrial function, tends to reduce the abundance of the organelle, through a vicious circle. J. Cell. Physiol. © 2011 Wiley-Liss, Inc. |
| Databáze: | OpenAIRE |
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