2026-05-22T02:01:23Zhttps://repisalud.isciii.es/rest/oai/requestoai:repisalud.isciii.es:20.500.12105/263632025-12-18T13:01:52Zcom_20.500.12105_2052com_20.500.12105_2051col_20.500.12105_19616col_20.500.12105_19617
Repisalud
author
Coronel Lopez, Raquel
author
García-Moreno, Enrique
author
Siendones, Emilio
author
Barrero, Maria
author
Martinez-Delgado, Beatriz
author
Santos-Ocaña, Carlos
author
Liste-Noya, Isabel
author
Cascajo-Almenara, M V
funder
Instituto de Salud Carlos III
funder
Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
2025-02-21T17:15:30Z
2025-02-21T17:15:30Z
2024
Coronel R, García-Moreno E, Siendones E, Barrero MJ, Martínez-Delgado B, Santos-Ocaña C, Liste I, Cascajo-Almenara MV. Brain organoid as a model to study the role of mitochondria in neurodevelopmental disorders: achievements and weaknesses. Front Cell Neurosci. 2024 Jun 24;18:1403734.
10.3389/fncel.2024.1403734
1662-5102
Frontiers in cellular neuroscience
38978706
https://hdl.handle.net/20.500.12105/26363
Mitochondrial diseases are a group of severe pathologies that cause complex neurodegenerative disorders for which, in most cases, no therapy or treatment is available. These organelles are critical regulators of both neurogenesis and homeostasis of the neurological system. Consequently, mitochondrial damage or dysfunction can occur as a cause or consequence of neurodevelopmental or neurodegenerative diseases. As genetic knowledge of neurodevelopmental disorders advances, associations have been identified between genes that encode mitochondrial proteins and neurological symptoms, such as neuropathy, encephalomyopathy, ataxia, seizures, and developmental delays, among others. Understanding how mitochondrial dysfunction can alter these processes is essential in researching rare diseases. Three-dimensional (3D) cell cultures, which self-assemble to form specialized structures composed of different cell types, represent an accessible manner to model organogenesis and neurodevelopmental disorders. In particular, brain organoids are revolutionizing the study of mitochondrial-based neurological diseases since they are organ-specific and model-generated from a patient's cell, thereby overcoming some of the limitations of traditional animal and cell models. In this review, we have collected which neurological structures and functions recapitulate in the different types of reported brain organoids, focusing on those generated as models of mitochondrial diseases. In addition to advancements in the generation of brain organoids, techniques, and approaches for studying neuronal structures and physiology, drug screening and drug repositioning studies performed in brain organoids with mitochondrial damage and neurodevelopmental disorders have also been reviewed. This scope review will summarize the evidence on limitations in studying the function and dynamics of mitochondria in brain organoids.
eng
3D cultures
Drug repurposing
High-throughput screening
Mitochondrial diseases
Neurodevelopmental disorders
Organoid
Spheroids
Brain organoid as a model to study the role of mitochondria in neurodevelopmental disorders: achievements and weaknesses
review article
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URL
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aadcd13a813697f405a5f67d49a7e0dd
3616518
application/pdf
BrainOrganoidModelStudy_2024.pdf