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Advances in mt-tRNA Mutation-Caused Mitochondrial Disease Modeling: Patients' Brain in a Dish

Authors :
Povea-Cabello, Suleva
Villanueva-Paz, Marina
Suarez-Rivero, Juan M.
Álvarez-Córdoba, Mónica
Villalón-García, Irene
Talaverón-Rey, Marta
Suárez-Carrillo, Alejandra
Munuera, Manuel
Sánchez-Alcázar, José Antonio
Instituto de Salud Carlos III
European Commission
Ministerio de Educación, Cultura y Deporte (España)
Asociación de Enfermos de Patologías Mitocondriales (España)
Source :
Digital.CSIC. Repositorio Institucional del CSIC, instname
Publication Year :
2021
Publisher :
Frontiers Media, 2021.

Abstract

© 2021 Povea-Cabello, Villanueva-Paz, Suárez-Rivero, Álvarez-Córdoba, Villalón-García, Talaverón-Rey, Suárez-Carrillo, Munuera-Cabeza and Sánchez-Alcázar. Mitochondrial diseases are a heterogeneous group of rare genetic disorders that can be caused by mutations in nuclear (nDNA) or mitochondrial DNA (mtDNA). Mutations in mtDNA are associated with several maternally inherited genetic diseases, with mitochondrial dysfunction as a main pathological feature. These diseases, although frequently multisystemic, mainly affect organs that require large amounts of energy such as the brain and the skeletal muscle. In contrast to the difficulty of obtaining neuronal and muscle cell models, the development of induced pluripotent stem cells (iPSCs) has shed light on the study of mitochondrial diseases. However, it is still a challenge to obtain an appropriate cellular model in order to find new therapeutic options for people suffering from these diseases. In this review, we deepen the knowledge in the current models for the most studied mt-tRNA mutation-caused mitochondrial diseases, MELAS (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes) and MERRF (myoclonic epilepsy with ragged red fibers) syndromes, and their therapeutic management. In particular, we will discuss the development of a novel model for mitochondrial disease research that consists of induced neurons (iNs) generated by direct reprogramming of fibroblasts derived from patients suffering from MERRF syndrome. We hypothesize that iNs will be helpful for mitochondrial disease modeling, since they could mimic patient’s neuron pathophysiology and give us the opportunity to correct the alterations in one of the most affected cellular types in these disorders. This work was supported by PI19/00377 grant, Instituto de Salud Carlos III, Spain, and Fondo Europeo de Desarrollo Regional (FEDER-Unión Europea), Spanish Ministry of Education, Culture and Sport, “Ayudas para la Formación de Profesorado Universitario” (FPU), and AEPMI (Asociación de Enfermos de Patología Mitocondrial).

Details

Database :
OpenAIRE
Journal :
Digital.CSIC. Repositorio Institucional del CSIC, instname
Accession number :
edsair.RECOLECTA.....26635b9589eb9e0cf69002b5cb97e3a4