Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathy
Articolo
Data di Pubblicazione:
2002
Abstract:
The possibility that some combinations of mtDNA polymorphisms, previously associated with Leber's hereditary optic neuropathy (LHON), may affect mitochondrial respiratory function was tested in osteosarcoma-derived transmitochondrial cytoplasmic hybrids (cybrids). In this cellular system, in the presence of the same nuclear background, different exogenous mtDNAs are used to repopulate a parental cell line previously devoid of its original mtDNA. No detectable differences in multiple parameters exploring respiratory function were observed when mtDNAs belonging to European haplogroups X, H, T and J were used. Different possible explanations for the previously established association between haplogroup J and LHON 11778/ND4 and 14484/ND6 pathogenic mutations are discussed, including the unconventional proposal that mtDNA haplogroup J may exert a protective rather than detrimental effect.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
HUMAN MTDNA; MITOCHONDRIAL HAPLOGROUPS; LEBER HEREDITARY OPTIC NEUROPATHY; LHON; CELL CYBRIDS
Elenco autori:
Carelli, V; Vergani, L; Bernazzi, B; Zampieron, C; Bucchi, L; Valentino, M; Rengo, Chiara; Torroni, Antonio; Martinuzzi, A.
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