RRC ID 86226
著者 Kawano S, Saegusa C, Masano Y, Becker F, Nakamura M, Shiozawa S, Fujikura J, Toyohara T, Abe T, Okano H, Fujioka M.
タイトル Modeling Mitochondrial Disease Using Brain Organoids: A Focus on Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes.
ジャーナル J Vis Exp
Abstract Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes (MELAS) are mitochondrial disorders most commonly caused by a m.3243A>G variant in mitochondrial tRNALeu. To investigate the pathophysiology of MELAS, we generated brain organoids from multiple induced pluripotent stem cell (iPSC) lines derived from a patient with MELAS carrying the m.3243A>G variant. These lines share an identical nuclear genetic background but differ in their heteroplasmy levels involving the m.3243A>G variant. We observed significant differences in organoid size, morphology, and neural induction efficiency, which correlated with the degree of heteroplasmy. Dissociated neurons from the organoids were transferred into a 2D-culture system, which is convenient and suitable for high-throughput drug screening. The organoids also exhibited significant differences in the formation of neural networks, depending on heteroplasmy levels. Our results suggest that patient-derived iPSC-based organoid models represent a useful platform for studying MELAS mechanisms and for drug screening. This video presents comprehensive and user-friendly methods, including protocols for generating organoids and evaluating phenotypes.
巻・号 (224)
公開日 2025-10-10
DOI 10.3791/69303
PMID 41144335
MeSH Brain* / pathology Humans Induced Pluripotent Stem Cells / cytology Induced Pluripotent Stem Cells / pathology MELAS Syndrome* / genetics MELAS Syndrome* / pathology MELAS Syndrome* / physiopathology Neurons / cytology Organoids* / pathology
IF 1.163
リソース情報
ヒト・動物細胞 414C2(HPS4292)