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The role of mitochondrial dysfunction in age-related diseases
The aging process is accompanied by the onset of disease and a general decline in wellness. Insights into the aging process have revealed a number of cellular hallmarks of aging, among these epigenetic alterations, loss of proteostasis, mitochondrial dysfunction, cellular senescence, and stem cell e...
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Published in: | Biochimica et biophysica acta 2015-11, Vol.1847 (11), p.1387-1400 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The aging process is accompanied by the onset of disease and a general decline in wellness. Insights into the aging process have revealed a number of cellular hallmarks of aging, among these epigenetic alterations, loss of proteostasis, mitochondrial dysfunction, cellular senescence, and stem cell exhaustion. Mitochondrial dysfunction increasingly appears to be a common factor connecting several of these hallmarks, driving the aging process and afflicting tissues throughout the body. Recent research has uncovered a much more complex involvement of mitochondria in the cell than has previously been appreciated and revealed novel ways in which mitochondrial defects feed into disease pathology. In this review we evaluate ways in which problems in mitochondria contribute to disease beyond the well-known mechanisms of oxidative stress and bioenergetic deficits, and we predict the direction that mitochondrial disease research will take in years to come.
•Mitochondrial dysfunction may be at the root of protein aggregation.•ROS signaling and metabolic restructuring are determinants of stem cell fate.•Mitochondria are central components of the innate immune response.•Deregulation of covalent modifications of mitochondrial proteins has been found in multiple diseases. |
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ISSN: | 0005-2728 0006-3002 1879-2650 1878-2434 |
DOI: | 10.1016/j.bbabio.2015.05.021 |