Related Experiment Video
Updated: Nov 11, 2025

Experimental Protocol for Detecting Mitochondrial Function in Hepatocytes Exposed to Organochlorine Pesticides
Published on: September 16, 2020
Targeting the Mitochondria-Proteostasis Axis to Delay Aging
Andreas Zimmermann1,2, Corina Madreiter-Sokolowski3, Sarah Stryeck4
1Institute of Molecular Biosciences, University of Graz, Graz, Austria.
Abstract:
Human life expectancy continues to grow globally, and so does the prevalence of age-related chronic diseases, causing a huge medical and economic burden on society. Effective therapeutic options for these disorders are scarce, and even if available, are typically limited to a single comorbidity in a multifaceted dysfunction that inevitably affects all organ systems. Thus, novel therapies that target fundamental processes of aging itself are desperately needed. In this article, we summarize current strategies that successfully delay aging and related diseases by targeting mitochondria and protein homeostasis. In particular, we focus on autophagy, as a fundamental proteostatic process that is intimately linked to mitochondrial quality control. We present genetic and pharmacological interventions that effectively extend health- and life-span by acting on specific mitochondrial and pro-autophagic molecular targets. In the end, we delve into the crosstalk between autophagy and mitochondria, in what we refer to as the mitochondria-proteostasis axis, and explore the prospect of targeting this crosstalk to harness maximal therapeutic potential of anti-aging interventions.
Insights
Strategies targeting mitochondria and protein homeostasis, particularly autophagy, can delay aging and related diseases. Interventions acting on the mitochondria-proteostasis axis offer promising therapeutic potential for extending healthspan.
Area of Science:
- Gerontology and cellular biology
- Molecular mechanisms of aging
Background:
- Increasing human life expectancy correlates with a rise in age-related chronic diseases, imposing significant societal burdens.
- Current treatments often address single comorbidities, lacking holistic approaches for multifaceted age-related dysfunctions.
- There is a critical need for novel therapies targeting the fundamental processes of aging itself.
Purpose of the Study:
- To summarize current anti-aging strategies focused on mitochondria and protein homeostasis.
- To highlight the role of autophagy in mitochondrial quality control and its link to aging.
- To explore the therapeutic potential of targeting the mitochondria-proteostasis axis.
Main Methods:
- Review of genetic and pharmacological interventions affecting aging.
- Focus on molecular targets within mitochondria and pathways promoting autophagy.
- Analysis of the interplay between mitochondria and protein homeostasis (autophagy).
Main Results:
- Specific interventions targeting mitochondria and pro-autophagic pathways demonstrate efficacy in extending healthspan and lifespan.
- Autophagy plays a crucial role in maintaining mitochondrial quality control.
- The crosstalk between mitochondria and autophagy, termed the mitochondria-proteostasis axis, is a key target.
Conclusions:
- Targeting mitochondria and protein homeostasis, especially autophagy, represents a viable strategy for combating age-related diseases.
- Interventions modulating the mitochondria-proteostasis axis hold significant promise for developing effective anti-aging therapies.
- Further research into this axis could unlock maximal therapeutic potential for extending human healthspan.
Related Concept Videos
Mitochondria
Electron Transport Chain: Complex I and II
ROS generation is regulated and maintained at moderate levels necessary...
Translocation of Proteins into the Mitochondria
Sorting of outer membrane proteins:
Mitochondrial outer membrane proteins are of two types: the transmembrane, beta-barrel porins, and the membrane-anchored, alpha-helical proteins. Beta-barrel porin precursors are translocated by the TOM complex and inserted into the outer mitochondrial membrane by the SAM complex. In contrast,...
Mitochondrial Membranes
Mitochondrial Precursor Proteins
Most of the mitochondrial...

