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Volumn 56, Issue 4, 2015, Pages 2269-2278

Changes in mitochondrial morphology and bioenergetics in human lymphoblastoid cells with four novel opa1 mutations

Author keywords

Autosomal dominant optic atrophy; Mitochondrial bioenergetics; Mitochondrial network; OPA1

Indexed keywords

ADENOSINE TRIPHOSPHATE; CHAPERONIN 60; ISOPROTEIN; MESSENGER RNA; REACTIVE OXYGEN METABOLITE; GUANOSINE TRIPHOSPHATASE; OPA1 PROTEIN, HUMAN;

EID: 84939623351     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.14-16288     Document Type: Article
Times cited : (26)

References (38)
  • 1
    • 0018397542 scopus 로고
    • Dominant optic atrophy. The clinical profile
    • Kline LB, Glaser JS. Dominant optic atrophy. The clinical profile. Arch Ophthalmol. 1979;97:1680-1686.
    • (1979) Arch Ophthalmol , vol.97 , pp. 1680-1686
    • Kline, L.B.1    Glaser, J.S.2
  • 3
    • 0036369531 scopus 로고    scopus 로고
    • Hamel CP OPA1 (Kjer type) dominant optic atrophy: A novel mitochondrial disease
    • Delettre C, Lenaers G, Pelloquin L, Belenguer P, Hamel CP OPA1 (Kjer type) dominant optic atrophy: a novel mitochondrial disease. Mol Genet Metab. 2002;75:97-107.
    • (2002) Mol Genet Metab , vol.75 , pp. 97-107
    • Delettre, C.1    Lenaers, G.2    Pelloquin, L.3    Belenguer, P.4
  • 5
    • 0020691778 scopus 로고
    • Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy
    • Kjer P, Jensen OA, Klinken L. Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy. Acta Ophthalmol (Copenh). 1983;61:300-312.
    • (1983) Acta Ophthalmol (Copenh) , vol.61 , pp. 300-312
    • Kjer, P.1    Jensen, O.A.2    Klinken, L.3
  • 6
    • 20244381365 scopus 로고    scopus 로고
    • Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy
    • Delettre C, Lenaers G, Griffoin JM, et al. Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy. Nat Genet. 2000;26:207-210.
    • (2000) Nat Genet , vol.26 , pp. 207-210
    • Delettre, C.1    Lenaers, G.2    Griffoin, J.M.3
  • 7
    • 0033772264 scopus 로고    scopus 로고
    • OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
    • Alexander C, Votruba M, Pesch UE, et al. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. Nat Genet. 2000; 26:211-215.
    • (2000) Nat Genet , vol.26 , pp. 211-215
    • Alexander, C.1    Votruba, M.2    Pesch, U.E.3
  • 9
    • 33745699393 scopus 로고    scopus 로고
    • OPA1 controls apoptotic cristae remodeling independently from mitochon-drial fusion
    • Frezza C, Cipolat S, Martins de Brito O, et al. OPA1 controls apoptotic cristae remodeling independently from mitochon-drial fusion. Cell. 2006;126:177-189.
    • (2006) Cell , vol.126 , pp. 177-189
    • Frezza, C.1    Cipolat, S.2    De Martins Brito, O.3
  • 11
    • 27444446030 scopus 로고    scopus 로고
    • Release of OPA1 during apoptosis participates in the rapid and complete release of cytochrome c and subsequent mitochondrial fragmentation
    • Arnoult D, Grodet A, Lee YJ, Estaquier J, Blackstone C. Release of OPA1 during apoptosis participates in the rapid and complete release of cytochrome c and subsequent mitochondrial fragmentation. JBiol Chem. 2005;280:35742-35750.
    • (2005) Jbiol Chem , vol.280 , pp. 35742-35750
    • Arnoult, D.1    Grodet, A.2    Lee, Y.J.3    Estaquier, J.4    Blackstone, C.5
  • 12
    • 0035683581 scopus 로고    scopus 로고
    • Mutation spectrum and splicing variants in the OPA1 gene
    • Delettre C, Griffoin JM, Kaplan J, et al. Mutation spectrum and splicing variants in the OPA1 gene. Hum Genet. 2001;109: 584-591.
    • (2001) Hum Genet , vol.109 , pp. 584-591
    • Delettre, C.1    Griffoin, J.M.2    Kaplan, J.3
  • 13
    • 3042533781 scopus 로고    scopus 로고
    • Developmental expression profile of the optic atrophy gene product: OPA1 is not localized exclusively in the mammalian retinal ganglion cell layer
    • Aijaz S, Erskine L, Jeffery G, Bhattacharya SS, Votruba M. Developmental expression profile of the optic atrophy gene product: OPA1 is not localized exclusively in the mammalian retinal ganglion cell layer. Invest Ophthalmol Vis Sci. 2004;45: 1667-1673.
    • (2004) Invest Ophthalmol Vis Sci , vol.45 , pp. 1667-1673
    • Aijaz, S.1    Erskine, L.2    Jeffery, G.3    Bhattacharya, S.S.4    Votruba, M.5
  • 14
    • 33748690957 scopus 로고    scopus 로고
    • OPA1 expression in the human retina and optic nerve
    • Wang AG, Fann MJ, Yu HY, Yen MY. OPA1 expression in the human retina and optic nerve. Exp Eye Res. 2006;83:1171-1178.
    • (2006) Exp Eye Res , vol.83 , pp. 1171-1178
    • Wang, A.G.1    Fann, M.J.2    Yu, H.Y.3    Yen, M.Y.4
  • 16
    • 43049117153 scopus 로고    scopus 로고
    • Metalloprotease-mediated OPA1 processing is modulated by the mitochondrial membrane potential
    • Guillery O, Malka F, Landes T, et al. Metalloprotease-mediated OPA1 processing is modulated by the mitochondrial membrane potential. Biol Cell. 2008;100:315-325.
    • (2008) Biol Cell , vol.100 , pp. 315-325
    • Guillery, O.1    Malka, F.2    Landes, T.3
  • 17
    • 84896264348 scopus 로고    scopus 로고
    • The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission
    • Anand R, Wai T, Baker MJ, et al. The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission. J Cell Biol. 2014;204:919-929.
    • (2014) J Cell Biol , vol.204 , pp. 919-929
    • Anand, R.1    Wai, T.2    Baker, M.J.3
  • 18
    • 33746299692 scopus 로고    scopus 로고
    • Regulationof mitochondrial morphology through proteolytic cleavage of OPA1
    • Ishihara N, Fujita Y, Oka T, Mihara K Regulationof mitochondrial morphology through proteolytic cleavage of OPA1. EMBO J. 2006;25:2966-2977.
    • (2006) EMBO J , vol.25 , pp. 2966-2977
    • Ishihara, N.1    Fujita, Y.2    Oka, T.3    Mihara, K.4
  • 19
    • 34548313688 scopus 로고    scopus 로고
    • OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L
    • Song Z, Chen H, Fiket M, Alexander C, Chan DC. OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L. JCell Biol. 2007;178:749-755.
    • (2007) Jcell Biol , vol.178 , pp. 749-755
    • Song, Z.1    Chen, H.2    Fiket, M.3    Alexander, C.4    Chan, D.C.5
  • 20
    • 33845976357 scopus 로고    scopus 로고
    • Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology
    • Duvezin-Caubet S, Jagasia R, Wagener J, et al. Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology. JBiol Chem. 2006; 281:37972-37979.
    • (2006) Jbiol Chem , vol.281 , pp. 37972-37979
    • Duvezin-Caubet, S.1    Jagasia, R.2    Wagener, J.3
  • 21
    • 84897538678 scopus 로고    scopus 로고
    • Proteolytic cleavage of Opa1 stimulates mitochondrial inner membrane fusion and couples fusion to oxidative phosphorylation
    • Mishra P, Carelli V, Manfredi G, Chan DC. Proteolytic cleavage of Opa1 stimulates mitochondrial inner membrane fusion and couples fusion to oxidative phosphorylation. Cell Metab. 2014;19:630-641.
    • (2014) Cell Metab , vol.19 , pp. 630-641
    • Mishra, P.1    Carelli, V.2    Manfredi, G.3    Chan, D.C.4
  • 22
    • 9144238312 scopus 로고    scopus 로고
    • Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy
    • Lodi R, Tonon C, Valentino ML, et al. Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy. Ann Neurol. 2004;56:719-723.
    • (2004) Ann Neurol , vol.56 , pp. 719-723
    • Lodi, R.1    Tonon, C.2    Valentino, M.L.3
  • 23
    • 54449084658 scopus 로고    scopus 로고
    • A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function
    • Spinazzi M, Cazzola S, Bortolozzi M, et al. A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function. Hum Mol Genet. 2008;17:3291-3302.
    • (2008) Hum Mol Genet , vol.17 , pp. 3291-3302
    • Spinazzi, M.1    Cazzola, S.2    Bortolozzi, M.3
  • 24
    • 38849190029 scopus 로고    scopus 로고
    • OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion
    • Zanna C, Ghelli A, Porcelli AM, et al. OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. Brain. 2008;131: 352-367.
    • (2008) Brain , vol.131 , pp. 352-367
    • Zanna, C.1    Ghelli, A.2    Porcelli, A.M.3
  • 25
    • 84864193527 scopus 로고    scopus 로고
    • Defective mitochondrial fusion, altered respiratory function, and distorted cristae structure in skin fibroblasts with heterozygous OPA1 mutations
    • Agier V, Oliviero P, Laine J, et al. Defective mitochondrial fusion, altered respiratory function, and distorted cristae structure in skin fibroblasts with heterozygous OPA1 mutations. Biochim Biophys Acta. 2012;1822:1570-1580.
    • (2012) Biochim Biophys Acta , vol.1822 , pp. 1570-1580
    • Agier, V.1    Oliviero, P.2    Laine, J.3
  • 26
    • 27544466847 scopus 로고    scopus 로고
    • Mitochondrial morphology and dynamics in yeast and multicellular eukaryotes
    • Okamoto K, Shaw JM. Mitochondrial morphology and dynamics in yeast and multicellular eukaryotes. Annu Rev Genet. 2005;39:503-536.
    • (2005) Annu Rev Genet , vol.39 , pp. 503-536
    • Okamoto, K.1    Shaw, J.M.2
  • 27
    • 22544451586 scopus 로고    scopus 로고
    • Disruption of fusion results in mitochondrial heterogeneity and dysfunction
    • Chen H, Chomyn A, Chan DC. Disruption of fusion results in mitochondrial heterogeneity and dysfunction. J Biol Chem. 2005;280:26185-26192.
    • (2005) J Biol Chem , vol.280 , pp. 26185-26192
    • Chen, H.1    Chomyn, A.2    Chan, D.C.3
  • 28
    • 75149120931 scopus 로고    scopus 로고
    • Novel mutations of the OPA1 gene in Chinese dominant optic atrophy
    • 392-396
    • Yen MY, Wang AG, Lin YC, Fann MJ, Hsiao KJ. Novel mutations of the OPA1 gene in Chinese dominant optic atrophy. Ophthalmology. 2010;117:392-396. e391.
    • (2010) Ophthalmology , pp. 391
    • Yen, M.Y.1    Wang, A.G.2    Lin, Y.C.3    Fann, M.J.4    Hsiao, K.J.5
  • 29
    • 0034881326 scopus 로고    scopus 로고
    • Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA
    • Nakada K, Inoue K, Ono T, et al. Inter-mitochondrial complementation: mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA. Nat Med. 2001;7:934-940.
    • (2001) Nat Med , vol.7 , pp. 934-940
    • Nakada, K.1    Inoue, K.2    Ono, T.3
  • 30
    • 79953659917 scopus 로고    scopus 로고
    • OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophy
    • Yu-Wai-Man P, Trenell MI, Hollingsworth KG, Griffiths PG, Chinnery PF. OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophy. Brain. 2011;134:e164.
    • (2011) Brain , vol.134
    • Yu-Wai-Man, P.1    Trenell, M.I.2    Hollingsworth, K.G.3    Griffiths, P.G.4    Chinnery, P.F.5
  • 31
    • 79959418295 scopus 로고    scopus 로고
    • Mitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophy
    • Van Bergen NJ, Crowston JG, Kearns LS, et al. Mitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophy. PLoS One. 2011;6:e21347.
    • (2011) Plos One , vol.6
    • Van Bergen, N.J.1    Crowston, J.G.2    Kearns, L.S.3
  • 33
    • 70350694223 scopus 로고    scopus 로고
    • Importance of the bioenergetic reserve capacity in response to cardiomyocyte stress induced by 4-hydroxynonenal
    • Hill BG, Dranka BP, Zou L, Chatham JC, Darley-Usmar VM. Importance of the bioenergetic reserve capacity in response to cardiomyocyte stress induced by 4-hydroxynonenal. Biochem J. 2009;424:99-107.
    • (2009) Biochem J , vol.424 , pp. 99-107
    • Hill, B.G.1    Dranka, B.P.2    Zou, L.3    Chatham, J.C.4    Darley-Usmar, V.M.5
  • 35
    • 80054051101 scopus 로고    scopus 로고
    • The regulation and physiology of mitochondrial proton leak
    • Divakaruni AS, Brand MD. The regulation and physiology of mitochondrial proton leak. Physiology (Bethesda). 2011;26: 192-205.
    • (2011) Physiology (Bethesda) , vol.26 , pp. 192-205
    • Divakaruni, A.S.1    Brand, M.D.2
  • 36
    • 0030995005 scopus 로고    scopus 로고
    • The physiological significance of mitochondrial proton leak in animal cells and tissues
    • Rolfe DF, Brand MD. The physiological significance of mitochondrial proton leak in animal cells and tissues. Biosci Rep. 1997;17:9-16.
    • (1997) Biosci Rep , vol.17 , pp. 9-16
    • Rolfe, D.F.1    Brand, M.D.2
  • 37
    • 84884909413 scopus 로고    scopus 로고
    • Mitochondrial cristae shape determines respiratory chain supercomplexes assembly and respiratory efficiency
    • Cogliati S, Frezza C, Soriano ME, et al. Mitochondrial cristae shape determines respiratory chain supercomplexes assembly and respiratory efficiency. Cell. 2013;155:160-171.
    • (2013) Cell , vol.155 , pp. 160-171
    • Cogliati, S.1    Frezza, C.2    Soriano, M.E.3


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