Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathy

被引:52
作者
Carelli, V
Vergani, L
Bernazzi, B
Zampieron, C
Bucchi, L
Valentino, ML
Rengo, C
Torroni, A
Martinuzzi, A
机构
[1] Conegliano Res Ctr, IRCCS E Medea Sci Inst, I-31015 Conegliano, TV, Italy
[2] Univ Bologna, Ist Clin Neurol, Bologna, Italy
[3] Univ Padua, Dipartimento Sci Neurol & Psichiatriche, Padua, Italy
[4] Univ Roma La Sapienza, Dipartimento Genet & Biol Mol, I-00185 Rome, Italy
[5] Univ Cattolica Sacro Cuore, Ist Med Legale, Rome, Italy
[6] Univ Pavia, Dipatimento Genet & Microbiol, I-27100 Pavia, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2002年 / 1588卷 / 01期
关键词
mtDNA; mitochondrial haplogroup; haplogroup J; LHON; cybrid;
D O I
10.1016/S0925-4439(02)00097-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:7 / 14
页数:8
相关论文
共 39 条
[1]   Titrating the effects of mitochondrial complex I impairment in the cell physiology [J].
Barrientos, A ;
Moraes, CT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (23) :16188-16197
[2]  
Brown MD, 1997, AM J HUM GENET, V60, P381
[3]   LEBER HEREDITARY OPTIC NEUROPATHY - A MODEL FOR MITOCHONDRIAL NEURODEGENERATIVE DISEASES [J].
BROWN, MD ;
VOLJAVEC, AS ;
LOTT, MT ;
MACDONALD, I ;
WALLACE, DC .
FASEB JOURNAL, 1992, 6 (10) :2791-2799
[4]  
BROWN MD, 1992, GENETICS, V130, P163
[5]   Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation [J].
Brown, MD ;
Trounce, IA ;
Jun, AS ;
Allen, JC ;
Wallace, DC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (51) :39831-39836
[6]   MITOCHONDRIAL-DNA AND HUMAN-EVOLUTION [J].
CANN, RL ;
STONEKING, M ;
WILSON, AC .
NATURE, 1987, 325 (6099) :31-36
[7]  
Carelli V, 1999, ANN NEUROL, V45, P320, DOI 10.1002/1531-8249(199903)45:3<320::AID-ANA7>3.3.CO
[8]  
2-C
[9]   Leber's hereditary optic neuropathy: Biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype [J].
Carelli, V ;
Ghelli, A ;
Ratta, M ;
Bacchilega, E ;
Sangiorgi, S ;
Mancini, R ;
Leuzzi, V ;
Cortelli, P ;
Montagna, P ;
Lugaresi, E ;
Esposti, MD .
NEUROLOGY, 1997, 48 (06) :1623-1632
[10]   Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient [J].
Carelli, V ;
Barboni, P ;
Zacchini, A ;
Mancini, R ;
Monari, L ;
Cevoli, S ;
Liguori, R ;
Sensi, M ;
Lugaresi, E ;
Montagna, P .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1998, 160 (02) :183-188