Mitochondrial quality control in AMD: does mitophagy play a pivotal role?
Juha M T HyttinenJohanna ViiriKai KaarnirantaJanusz BłasiakPublished in: Cellular and molecular life sciences : CMLS (2018)
Age-related macular degeneration (AMD) is the predominant cause of visual loss in old people in the developed world, whose incidence is increasing. This disease is caused by the decrease in macular function, due to the degeneration of retinal pigment epithelium (RPE) cells. The aged retina is characterised by increased levels of reactive oxygen species (ROS), impaired autophagy, and DNA damage that are linked to AMD pathogenesis. Mitophagy, a mitochondria-specific type of autophagy, is an essential part of mitochondrial quality control, the collective mechanism responsible for this organelle's homeostasis. The abundance of ROS, DNA damage, and the excessive energy consumption in the ageing retina all contribute to the degeneration of RPE cells and their mitochondria. We discuss the role of mitophagy in the cell and argue that its impairment may play a role in AMD pathogenesis. Thus, mitophagy as a potential therapeutic target in AMD and other degenerative diseases is as well explored.
Keyphrases
- age related macular degeneration
- dna damage
- quality control
- reactive oxygen species
- oxidative stress
- cell death
- induced apoptosis
- cell cycle arrest
- endoplasmic reticulum stress
- signaling pathway
- dna repair
- nlrp inflammasome
- diabetic retinopathy
- single cell
- body mass index
- risk factors
- climate change
- cell proliferation
- stem cells
- optic nerve
- pi k akt
- bone marrow
- microbial community