Javascript must be enabled to continue!
Effect of mitochondrial circulation on mitochondrial age density distribution
View through CrossRef
AbstractRecent publications report that although the mitochondria population in an axon can be quickly replaced by a combination of retrograde and anterograde axonal transport (often within less than 24 hours), the axon contains much older mitochondria. This suggests that not all mitochondria that reach the soma are degraded and that some are recirculating back into the axon. To explain this, we developed a model that simulates mitochondria distribution when a portion of mitochondria that return to the soma are redirected back to the axon rather than being destroyed in somatic lysosomes. Utilizing the developed model, we studied how the percentage of returning mitochondria affects the mean age and age density distributions of mitochondria at different distances from the soma. We also investigated whether turning off the mitochondrial anchoring switch can reduce the mean age of mitochondria. For this purpose, we studied the effect of reducing the value of a parameter that characterizes the probability of mitochondria transition to the stationary (anchored) state. The reduction in mitochondria mean age observed when the anchoring probability is reduced suggests that some injured neurons may be saved if the percentage of stationary mitochondria is decreased. The replacement of possibly damaged stationary mitochondria with newly synthesized ones may restore the energy supply in an injured axon. We also performed a sensitivity study of the mean age of stationary mitochondria to the parameter that determines what portion of mitochondria re-enter the axon and the parameter that determines the probability of mitochondria transition to the stationary state.
Title: Effect of mitochondrial circulation on mitochondrial age density distribution
Description:
AbstractRecent publications report that although the mitochondria population in an axon can be quickly replaced by a combination of retrograde and anterograde axonal transport (often within less than 24 hours), the axon contains much older mitochondria.
This suggests that not all mitochondria that reach the soma are degraded and that some are recirculating back into the axon.
To explain this, we developed a model that simulates mitochondria distribution when a portion of mitochondria that return to the soma are redirected back to the axon rather than being destroyed in somatic lysosomes.
Utilizing the developed model, we studied how the percentage of returning mitochondria affects the mean age and age density distributions of mitochondria at different distances from the soma.
We also investigated whether turning off the mitochondrial anchoring switch can reduce the mean age of mitochondria.
For this purpose, we studied the effect of reducing the value of a parameter that characterizes the probability of mitochondria transition to the stationary (anchored) state.
The reduction in mitochondria mean age observed when the anchoring probability is reduced suggests that some injured neurons may be saved if the percentage of stationary mitochondria is decreased.
The replacement of possibly damaged stationary mitochondria with newly synthesized ones may restore the energy supply in an injured axon.
We also performed a sensitivity study of the mean age of stationary mitochondria to the parameter that determines what portion of mitochondria re-enter the axon and the parameter that determines the probability of mitochondria transition to the stationary state.
Related Results
Mitochondria Fusion and Fission
Mitochondria Fusion and Fission
Abstract
Mitochondrial structural dynamics is regulated by the fusion or fission of these organelles. Recently published evidence indicates the ...
Fundamental Concepts and Methodology for the Analysis of Animal Population Dynamics, with Particular Reference to Univoltine Species
Fundamental Concepts and Methodology for the Analysis of Animal Population Dynamics, with Particular Reference to Univoltine Species
This paper presents some concepts and methodology essential for the analysis of population dynamics of univoltine species. Simple stochastic difference equations, comprised of endo...
Study on Structure Parameters of Reverse Circulation Drill Bit Secondary Injector Device Based on Injector Coefficient
Study on Structure Parameters of Reverse Circulation Drill Bit Secondary Injector Device Based on Injector Coefficient
Abstract
The hollow-through DTH hammer reverse circulation continuous coring drilling technology has been successfully applied to well drilling. During its applicati...
GW24-e3762 Role Of mitochondrial fission In cardiac microvascular endothelial cells after ischaemia/reperfusion
GW24-e3762 Role Of mitochondrial fission In cardiac microvascular endothelial cells after ischaemia/reperfusion
Objectives
This study is aimed to establish a simulated ischaemia/reperfusion (SI/R) model in cultured CMECs from adult rat, and investigate the role of mitochond...
Principles of the mitochondrial fusion and fission cycle in neurons
Principles of the mitochondrial fusion and fission cycle in neurons
Mitochondrial fusion-fission dynamics play a crucial role in many important cell processes. These dynamics control mitochondrial morphology, which in turn influences several import...
Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations
Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations
A number of human diseases are caused by inherited mitochondrial DNA mutations. Two of these diseases, MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-lik...
Abstract 283: SGK1-Dependent Sirt3 Phosphorylation Regulates Mitochondrial Dynamics
Abstract 283: SGK1-Dependent Sirt3 Phosphorylation Regulates Mitochondrial Dynamics
Mitochondrial dynamics (i.e. fusion and fission) is impaired in models of obesity and can result in target organ dysfunction. However, the mechanisms that regulate mitochondrial dy...
Defective mitochondrial-lysosomal axis promotes extracellular vesicles release of mitochondrial components in Huntington’s Disease
Defective mitochondrial-lysosomal axis promotes extracellular vesicles release of mitochondrial components in Huntington’s Disease
ABSTRACTMitochondrial and autophagy dysfunction are mechanisms proposed to be involved in the pathogenesis of several neurodegenerative diseases. Huntington’s disease (HD) is a pro...

