Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome.

Federico Sadun, Valerio Carelli, Raffaele Lodi, Paolo Pinton, Carlotta Giorgi, Caterina Tonon, Rocco Liguori, Maria Lucia Valentino, Claudio Bianchini, Stefania Evangelisti, Giacomo Savini, Piero Barboni, Chiara La Morgia, Mariantonietta Capristo, Valentina Del Dotto, Francesca Tagliavini, Leonardo Caporali, Simone Patergnani, Alberto Danese, Emanuela Scimonelli, Michele Carbonelli, Laura Ludovica Gramegna, Giulia Amore, Alessandra Maresca

Journal: Scientific reports 2020;10(1):4785

PMID: 32179840

Abstract

Wolfram syndrome (WS) is a recessive multisystem disorder defined by the association of diabetes mellitus and optic atrophy, reminiscent of mitochondrial diseases. The role played by mitochondria remains elusive, with contradictory results on the occurrence of mitochondrial dysfunction. We evaluated 13 recessive WS patients by deep clinical phenotyping, including optical coherence tomography (OCT), serum lactic acid at rest and after standardized exercise, brain Magnetic Resonance Imaging, and brain and muscle Magnetic Resonance Spectroscopy (MRS). Finally, we investigated mitochondrial bioenergetics, network morphology, and calcium handling in patient-derived fibroblasts. Our results do not support a primary mitochondrial dysfunction in WS patients, as suggested by MRS studies, OCT pattern of retinal nerve fiber layer loss, and, in fibroblasts, by mitochondrial bioenergetics and network morphology results. However, we clearly found calcium mishandling between endoplasmic reticulum (ER) and mitochondria, which, under specific metabolic conditions of increased energy requirements and in selected tissue or cell types, may turn into a secondary mitochondrial dysfunction. Critically, we showed that Wolframin (WFS1) protein is enriched at mitochondrial-associated ER membranes and that in patient-derived fibroblasts WFS1 protein is completely absent. These findings support a loss-of-function pathogenic mechanism for missense mutations in WFS1, ultimately leading to defective calcium influx within mitochondria.

Address: IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna, Italy. [email protected].; Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy. [email protected].; IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna, Italy.; Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy.; IRCCS Istituto delle Scienze Neurologiche di Bologna, UO Diagnostica Funzionale Neuroradiologica, Bologna, Italy.; Department of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, Laboratory for Technologies of Advanced Therapies (LTTA), University of Ferrara, Ferrara, Italy.; Maria Cecilia Hospital, GVM Care & Research, 48033, Cotignola, Ravenna, Italy.; Ospedale Oftalmico Roma, Rome, Italy.; Studio Oculistico D'Azeglio, Bologna, Italy.; IRCCS G.B. Bietti Foundation, Rome, Italy.
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