Artikel ; Online: Mitochondrial dysfunction characterized in human induced pluripotent stem cell disease models in MELAS syndrome: A brief summary.
2023 Band 72, Seite(n) 102–105
Abstract: Human induced pluripotent stem cells (hiPSCs) for MELAS syndrome (mitochondrial myopathy, encephalopathy, lactic acidosis, stroke-like episodes) may allow deeper understanding of how tissue-specific mitochondrial dysfunction result in multi-systemic ... ...
Abstract | Human induced pluripotent stem cells (hiPSCs) for MELAS syndrome (mitochondrial myopathy, encephalopathy, lactic acidosis, stroke-like episodes) may allow deeper understanding of how tissue-specific mitochondrial dysfunction result in multi-systemic disease. Here, we summarize how the m.3243G mtDNA mutation affects mitochondrial function in different tissues using iPSC and iPSC-differentiated cell type disease models and what significant findings have been replicated in the independent studies. Through this brief review and with a focus on mitochondrial dysfunction in iPSC-differentiated cell types, namely fibroblast, neuron, and retinal pigment epithelium cells, we aim to bring awareness of hiPSC as a robust mitochondrial disease model even if many unanswered questions remain. |
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Mesh-Begriff(e) | Humans ; MELAS Syndrome/genetics ; Induced Pluripotent Stem Cells ; Acidosis, Lactic ; Cell Differentiation ; Mitochondria |
Sprache | Englisch |
Erscheinungsdatum | 2023-08-25 |
Erscheinungsland | Netherlands |
Dokumenttyp | Review ; Journal Article |
ZDB-ID | 2056923-3 |
ISSN | 1872-8278 ; 1567-7249 |
ISSN (online) | 1872-8278 |
ISSN | 1567-7249 |
DOI | 10.1016/j.mito.2023.08.003 |
Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
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