Cellular and Molecular Responses to Mitochondrial DNA Deletions in Kearns-Sayre Syndrome: Some Underlying Mechanisms.
Mazyar YazdaniPublished in: Molecular neurobiology (2024)
Kearns-Sayre syndrome (KSS) is a rare multisystem mitochondrial disorder. It is caused by mitochondrial DNA (mtDNA) rearrangements, mostly large-scale deletions of 1.1-10 kb. These deletions primarily affect energy supply through impaired oxidative phosphorylation and reduced ATP production. This impairment gives rise to dysfunction of several tissues, in particular those with high energy demand like brain and muscles. Over the past decades, changes in respiratory chain complexes and energy metabolism have been emphasized, whereas little attention has been paid to other reports on ROS overproduction, protein synthesis inhibition, myelin vacuolation, demyelination, autophagy, apoptosis, and involvement of lipid raft and oligodendrocytes in KSS. Therefore, this paper draws attention towards these relatively underemphasized findings that might further clarify the pathologic cascades following deletions in the mtDNA.
Keyphrases
- mitochondrial dna
- copy number
- oxidative stress
- cell death
- working memory
- endoplasmic reticulum stress
- white matter
- dna damage
- case report
- signaling pathway
- cell cycle arrest
- neoadjuvant chemotherapy
- reactive oxygen species
- resting state
- radiation therapy
- multiple sclerosis
- dna methylation
- emergency department
- fatty acid
- functional connectivity
- locally advanced
- drug induced