Ludwig-Maximilians-Universität, Chair of Metabolic Biochemistry

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Tau-induced mitochondrial membrane perturbation is dependent upon cardiolipin

Biochim Biophys Acta Biomembr. 2020 Feb 1;1862(2):183064

Authors/Editors: Angelique Camilleri
Stephanie Ghio
Mario Caruana
Daniel Weckbecker
Felix Schmidt
Frits Kamp
Andrei Leonov
Sergey Ryazanov
Christian Griesinger
Armin Giese
Ruben J Cauchi
Neville Vassallo
Publication Date: 2020
Type of Publication: Journal Article

Misfolding and aggregate formation by the tau protein has been closely related with neurotoxicity in a large group of human neurodegenerative disorders, which includes Alzheimer's disease. Here, we investigate the membrane-active properties of tau oligomers on mitochondrial membranes, using minimalist in vitro model systems. Thus, exposure of isolated mitochondria to oligomeric tau evoked a disruption of mitochondrial membrane integrity, as evidenced by a combination of organelle swelling, efflux of cytochrome c and loss of the mitochondrial membrane potential. Tau-induced mitochondrial dysfunction occurred independently of the mitochondrial permeability transition (mPT) pore complex. Notably, mitochondria were rescued by pre-incubation with 10-N-nonyl acridine orange (NAO), a molecule that specifically binds cardiolipin (CL), the signature phospholipid of mitochondrial membranes. Additionally, NAO prevented direct binding of tau oligomers to isolated mitochondria. At the same time, tau proteins exhibited high affinity to CL-enriched membranes, whilst permeabilisation of lipid vesicles also strongly correlated with CL content. Intriguingly, using single-channel electrophysiology, we could demonstrate the formation of non-selective ion-conducting tau nanopores exhibiting multilevel conductances in mito-mimetic bilayers. Taken together, the data presented here advances a scenario in which toxic cytosolic entities of tau protein would target mitochondrial organelles by associating with their CL-rich membrane domains, leading to membrane poration and compromised mitochondrial structural integrity.

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