4.6 Article

Mitochondrial replacement in an iPSC model of Leber's hereditary optic neuropathy

期刊

AGING-US
卷 9, 期 4, 页码 1341-1350

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/aging.101231

关键词

Leber's hereditary optic neuropathy; disease model; induced pluripotent stem cells; retinal ganglion cells; cybrid

资金

  1. National Health and Medical Research Council (NHMRC) [1084256]
  2. Australian Mitochondrial Disease Foundation
  3. Brockhoff foundation
  4. University of Melbourne
  5. Ophthalmic Research Institute of Australia
  6. NHMRC Practitioner Fellowship [APP1103329]
  7. Australian Research Council Future Fellowship [FT140100047]
  8. Peggy and Leslie Cranbourne Foundation Fellowship
  9. Medical Advances Without Animals Trust Fellowship
  10. Victorian Government
  11. National Health and Medical Research Council of Australia [1084256] Funding Source: NHMRC

向作者/读者索取更多资源

Cybrid technology was used to replace Leber hereditary optic neuropathy (LHON) causing mitochondrial DNA (mtDNA) mutations from patient-specific fibroblasts with wildtype mtDNA, and mutation-free induced pluripotent stem cells (iPSCs) were generated subsequently. Retinal ganglion cell (RGC) differentiation demonstrates increased cell death in LHON-RGCs and can be rescued in cybrid corrected RGCs.

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