Mitochondrial and Cellular Function in Fibroblasts, Induced Neurons, and Astrocytes Derived from Case Study Patients: Insights into Major Depression as a Mitochondria-Associated Disease

Author:

Cardon Iseline1ORCID,Grobecker Sonja1,Kücükoktay Selin1,Bader Stefanie1ORCID,Jahner Tatjana1,Nothdurfter Caroline1,Koschitzki Kevin2ORCID,Berneburg Mark2,Weber Bernhard H. F.34,Stöhr Heidi3ORCID,Höring Marcus5ORCID,Liebisch Gerhard5ORCID,Braun Frank6,Rothammer-Hampl Tanja6,Riemenschneider Markus J.6,Rupprecht Rainer1,Milenkovic Vladimir M.1ORCID,Wetzel Christian H.1ORCID

Affiliation:

1. Department of Psychiatry and Psychotherapy, University of Regensburg, 93053 Regensburg, Germany

2. Department of Dermatology, Regensburg University Hospital, 93053 Regensburg, Germany

3. Institute of Human Genetics, University of Regensburg, 93053 Regensburg, Germany

4. Institute of Clinical Human Genetics, Regensburg University Hospital, 93053 Regensburg, Germany

5. Institute of Clinical Chemistry and Laboratory Medicine, Regensburg University Hospital, 93053 Regensburg, Germany

6. Department of Neuropathology, Regensburg University Hospital, 93053 Regensburg, Germany

Abstract

The link between mitochondria and major depressive disorder (MDD) is increasingly evident, underscored both by mitochondria’s involvement in many mechanisms identified in depression and the high prevalence of MDD in individuals with mitochondrial disorders. Mitochondrial functions and energy metabolism are increasingly considered to be involved in MDD’s pathogenesis. This study focused on cellular and mitochondrial (dys)function in two atypical cases: an antidepressant non-responding MDD patient (“Non-R”) and another with an unexplained mitochondrial disorder (“Mito”). Skin biopsies from these patients and controls were used to generate various cell types, including astrocytes and neurons, and cellular and mitochondrial functions were analyzed. Similarities were observed between the Mito patient and a broader MDD cohort, including decreased respiration and mitochondrial function. Conversely, the Non-R patient exhibited increased respiratory rates, mitochondrial calcium, and resting membrane potential. In conclusion, the Non-R patient’s data offered a new perspective on MDD, suggesting a detrimental imbalance in mitochondrial and cellular processes, rather than simply reduced functions. Meanwhile, the Mito patient’s data revealed the extensive effects of mitochondrial dysfunctions on cellular functions, potentially highlighting new MDD-associated impairments. Together, these case studies enhance our comprehension of MDD.

Funder

Deutsche Forschungsgemeinschaft

Bavarian State Ministry of Science and the Arts

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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