Mitochondria–Endoplasmic Reticulum Contact Sites Dynamics and Calcium Homeostasis Are Differentially Disrupted in PINK1‐PD or PRKN‐PD Neurons

Author:

Grossmann Dajana1ORCID,Malburg Nina1,Glaß Hannes1ORCID,Weeren Veronika1,Sondermann Verena1,Pfeiffer Julia F.1,Petters Janine1,Lukas Jan12ORCID,Seibler Philip3ORCID,Klein Christine3ORCID,Grünewald Anne34ORCID,Hermann Andreas125ORCID

Affiliation:

1. Translational Neurodegeneration Section “Albrecht Kossel,” Department of Neurology University Medical Center Rostock, University of Rostock Rostock Germany

2. Center for Transdisciplinary Neurosciences Rostock University Medical Center Rostock, University of Rostock Rostock Germany

3. Institute of Neurogenetics University of Lübeck Lübeck Germany

4. Luxembourg Centre for Systems Biomedicine University of Luxembourg Belvaux Luxembourg

5. Deutsches Zentrum für Neurodegenerative Erkrankungen Rostock/Greifswald Rostock Germany

Abstract

AbstractBackgroundIt is generally believed that the pathogenesis of PINK1/parkin‐related Parkinson's disease (PD) is due to a disturbance in mitochondrial quality control. However, recent studies have found that PINK1 and Parkin play a significant role in mitochondrial calcium homeostasis and are involved in the regulation of mitochondria–endoplasmic reticulum contact sites (MERCSs).ObjectiveThe aim of our study was to perform an in‐depth analysis of the role of MERCSs and impaired calcium homeostasis in PINK1/Parkin‐linked PD.MethodsIn our study, we used induced pluripotent stem cell–derived dopaminergic neurons from patients with PD with loss‐of‐function mutations in PINK1 or PRKN. We employed a split‐GFP‐based contact site sensor in combination with the calcium‐sensitive dye Rhod‐2 AM and applied Airyscan live‐cell super‐resolution microscopy to determine how MERCSs are involved in the regulation of mitochondrial calcium homeostasis.ResultsOur results showed that thapsigargin‐induced calcium stress leads to an increase of the abundance of narrow MERCSs in wild‐type neurons. Intriguingly, calcium levels at the MERCSs remained stable, whereas the increased net calcium influx resulted in elevated mitochondrial calcium levels. However, PINK1‐PD or PRKN‐PD neurons showed an increased abundance of MERCSs at baseline, accompanied by an inability to further increase MERCSs upon thapsigargin‐induced calcium stress. Consequently, calcium distribution at MERCSs and within mitochondria was disrupted.ConclusionsOur results demonstrated how the endoplasmic reticulum and mitochondria work together to cope with calcium stress in wild‐type neurons. In addition, our results suggests that PRKN deficiency affects the dynamics and composition of MERCSs differently from PINK1 deficiency, resulting in differentially affected calcium homeostasis. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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