Stress at the gates: Mitochondrial import dysfunctions, response pathways, and therapeutic potential

Dec 6, 2025Mitochondrion

Problems with Mitochondrial Protein Entry, Stress Responses, and Possible Treatments

AI simplified

Longevity & Aging on OpenScience ↗PubMed ↗DOI ↗

Abstract

Mitochondrial protein import is essential for the proper functioning of the organelle, involving over 1000 proteins synthesized in the cytosol.

Mitochondrial proteins are imported through specific translocases, including TOMM and TIMM complexes.
Import deficiencies may activate stress response pathways to restore cellular balance.
Four interconnected pathways are involved in compensating for import alterations: DELE1-HRI axis with ISR, UPRam, UPRmt, and mitophagy.
Low stress conditions activate ISR and UPRmt pathways, while high stress triggers mitophagy to eliminate dysfunctional mitochondria.
Mitochondrial import deficiencies are associated with various diseases, including neurodegenerative disorders and cancer.
Pharmacological compounds mimicking stress response mechanisms could offer future therapeutic options to enhance mitochondrial protein import.

AI simplified

Mitochondrial protein import is necessary to ensure the proper functioning of the organelle of the cell as a whole. More than 1000 proteins are synthesized on cytosolic ribosomes and then imported into mitochondria through translocases such as TOMM and TIMM complexes. Upon entry, they can reach their final mitochondrial compartment, namely the outer mitochondrial membrane (OMM), the intermembrane space (IMS), the inner mitochondrial membrane (IMM), and the matrix. In this review, we will first explore the main mitochondrial protein import mechanisms. Then, we will focus on how import deficiencies may trigger stress paradigms. Stress response pathways are activated to restore correct cellular homeostasis. We will explore four interconnected pathways at the cellular or mitochondrial scale, which can compensate for import alterations. These are the DELE1-HRI axis combined with the ISR, the UPRam, the UPRmt, and mitophagy. Their activation depends on the extent of import alteration, with ISR and UPRmt pathways activated in conditions of low stress. If stress levels are too high, the elimination of dysfunctional mitochondria by mitophagy is triggered. Last, we will explore how mitochondrial import deficiencies are a feature common to multifaceted pathologies, such as neurodegenerative diseases and cancer. We will also present pharmacological compounds mimicking stress response mechanisms and that could be used as a therapeutic option in the near future to restore efficient mitochondrial protein import rates. Overall, this review highlights the critical role of mitochondrial protein import in cellular and mitochondrial stress response, and in disease pathogenesis. It also emphasizes the potential of mitochondrial protein import as a therapeutic target, despite the surprising absence of direct pharmacological treatments to date.

Full Text

Full text is available at the source.

View full text (XML) ↗View full text ↗

Stress at the gates: Mitochondrial import dysfunctions, response pathways, and therapeutic potential

Abstract

Full Text

You found one interesting study. We’ll send the next 7.

what lands in your inbox each week:

Recent issues from the longevity & aging brief

Abstract

Full Text

Related papers

You found one interesting study. We’ll send the next 7.

what lands in your inbox each week:

Recent issues from the longevity & aging brief