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plamartinlab

How cells decide which mitochondria to keep - and which to discard.

PLA MARTÍN LAB - INSTITUTE OF BIOCHEMISTRY AND MOLECULAR BIOLOGY I
UNIVERSITÄTSKLINIKUM DÜSSELDORF - HEINRICH HEINE UNIVERSITÄT

Mitochondria are multifaceted organelles involved in many critical functions essential for cellular homeostasis. They form a highly dynamic network that is constantly remodeled, adapting its function in real time to cellular needs. Uniquely among organelles, mitochondria contain their own genome, mitochondrial DNA (mtDNA), which encodes 13 protein-coding genes of the oxidative phosphorylation (OXPHOS) machinery. Preserving both the structural and genetic integrity of mitochondria is therefore essential for sustained mitochondrial and cellular function.

Research

Our research focus

Our group aims to understand how mitochondrial (dys)function drives disease. We focus on how cells maintain, recognise and eliminate damaged mitochondrial DNA, and how failures in these processes contribute to neurodegeneration, ageing and cancer. Our work follows four main research lines.

QUALITY CONTROL

Selective mtDNA degradation

How cells recognize, traffic and eliminate damaged mitochondrial DNA, and how mitochondria, endosomes and lysosomes work together to keep mtDNA intact.

NEUROBIOLOGY

Mitochondrial Charcot-Marie-Tooth disease

How changes in mitochondrial and lysosomal proteins drive peripheral nerve degeneration, with a focus on CMT caused by mutations in GDAP1 and SBF1.

AGEING & METABOLISM

mtDNA instability and cellular integrity

How defects in mtDNA replication and maintenance affect cell homeostasis, stress responses and tissue function, in metabolism, ageing and neurodegeneration.

CANCER

Mitochondria in lymphoma

How lymphoma cells remodel their  mitochondrial metabolism to grow, survive and adapt to stress, and where this opens new therapeutic vulnerabilities.

I am Professor of Mitochondrial Biology and Metabolism at the Institute of Biochemistry and Molecular Biology I, Heinrich Heine University Düsseldorf. After my PhD in Valencia and postdoctoral years in Cologne, I took up my chair in 2023. What drives our work is a simple question: how does a cell decide what to keep and what to discard?

SELECTED PUBLICATIONS

Recent work

Retromer promotes the lysosomal turnover of mtDNA

Kakanj P, Bones M, … Pla-Martín D · Science Advances · 2025

Mitochondrial membrane proteins and VPS35 orchestrate selective removal of mtDNA

Sen A, Kallabis S, … Pla-Martín D · Nature Communications · 2022