메뉴 건너뛰기




Volumn 25, Issue 3, 2016, Pages 514-523

SMN deficiency does not induce oxidative stress in SMA iPSC-derived astrocytes or motor neurons

Author keywords

[No Author keywords available]

Indexed keywords

8 HYDROXYDEOXYGUANOSINE; CATALASE; OXYGEN; REACTIVE OXYGEN METABOLITE; SURVIVAL MOTOR NEURON PROTEIN; GCLC PROTEIN, HUMAN; GLUTAMATE CYSTEINE LIGASE; GLUTATHIONE PEROXIDASE; GLUTATHIONE PEROXIDASE 1; NFE2L2 PROTEIN, HUMAN; NQO1 PROTEIN, HUMAN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE (PHOSPHATE) DEHYDROGENASE (QUINONE); SMALL INTERFERING RNA; SUPEROXIDE DISMUTASE; TRANSCRIPTION FACTOR NRF2;

EID: 84960888922     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddv489     Document Type: Article
Times cited : (30)

References (54)
  • 3
    • 0033033434 scopus 로고    scopus 로고
    • A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy
    • Lorson, C.L., Hahnen, E., Androphy, E.J. and Wirth, B. (1999) A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy. Proc. Natl Acad. Sci. USA., 96, 6307-6311.
    • (1999) Proc. Natl Acad. Sci. USA , vol.96 , pp. 6307-6311
    • Lorson, C.L.1    Hahnen, E.2    Androphy, E.J.3    Wirth, B.4
  • 4
    • 0033983258 scopus 로고    scopus 로고
    • An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMN
    • Lorson, C.L. and Androphy, E.J. (2000) An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMN. Hum. Mol. Genet., 9, 259-265.
    • (2000) Hum. Mol. Genet , vol.9 , pp. 259-265
    • Lorson, C.L.1    Androphy, E.J.2
  • 5
    • 77955894067 scopus 로고    scopus 로고
    • Antisense correction of SMN2 splicing in the CNS rescues necrosis in a type III SMA mouse model
    • Hua, Y., Sahashi, K., Hung, G., Rigo, F., Passini, M.A., Bennett, C.F. and Krainer, A.R. (2010) Antisense correction of SMN2 splicing in the CNS rescues necrosis in a type III SMA mouse model. Genes. Dev., 24, 1634-1644.
    • (2010) Genes. Dev , vol.24 , pp. 1634-1644
    • Hua, Y.1    Sahashi, K.2    Hung, G.3    Rigo, F.4    Passini, M.A.5    Bennett, C.F.6    Krainer, A.R.7
  • 6
    • 84877859235 scopus 로고    scopus 로고
    • Antisense oligonucleotides for the treatment of spinal muscular atrophy
    • Porensky, P.N. and Burghes, A.H. (2013) Antisense oligonucleotides for the treatment of spinal muscular atrophy. Hum. Gene. Ther., 24, 489-498.
    • (2013) Hum. Gene. Ther , vol.24 , pp. 489-498
    • Porensky, P.N.1    Burghes, A.H.2
  • 12
    • 77955602597 scopus 로고    scopus 로고
    • Systemic delivery of scAAV9 expressing SMN prolongs survival in a model of spinal muscular atrophy
    • Valori, C.F., Ning, K., Wyles, M., Mead, R.J., Grierson, A.J., Shaw, P.J. and Azzouz, M. (2010) Systemic delivery of scAAV9 expressing SMN prolongs survival in a model of spinal muscular atrophy. Sci. Transl. Med., 2, 35ra42.
    • (2010) Sci. Transl. Med , vol.2
    • Valori, C.F.1    Ning, K.2    Wyles, M.3    Mead, R.J.4    Grierson, A.J.5    Shaw, P.J.6    Azzouz, M.7
  • 13
    • 84858026947 scopus 로고    scopus 로고
    • Decreasing disease severity in symptomatic, Smn(-/-);SMN2(+/+), spinal muscular atrophy mice following scAAV9-SMN delivery
    • Glascock, J.J., Osman, E.Y., Wetz, M.J., Krogman, M.M., Shababi, M. and Lorson, C.L. (2012) Decreasing disease severity in symptomatic, Smn(-/-);SMN2(+/+), spinal muscular atrophy mice following scAAV9-SMN delivery. Hum. Gene. Ther., 23, 330-335.
    • (2012) Hum. Gene. Ther , vol.23 , pp. 330-335
    • Glascock, J.J.1    Osman, E.Y.2    Wetz, M.J.3    Krogman, M.M.4    Shababi, M.5    Lorson, C.L.6
  • 16
    • 20144385587 scopus 로고    scopus 로고
    • SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN
    • Le, T.T., Pham, L.T., Butchbach, M.E., Zhang, H.L., Monani, U. R., Coovert, D.D., Gavrilina, T.O., Xing, L., Bassell, G.J. and Burghes, A.H. (2005) SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN. Hum. Mol. Genet., 14, 845-857.
    • (2005) Hum. Mol. Genet , vol.14 , pp. 845-857
    • Le, T.T.1    Pham, L.T.2    Butchbach, M.E.3    Zhang, H.L.4    Monani, U.R.5    Coovert, D.D.6    Gavrilina, T.O.7    Xing, L.8    Bassell, G.J.9    Burghes, A.H.10
  • 18
    • 67651083390 scopus 로고    scopus 로고
    • Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?
    • Burghes, A.H. and Beattie, C.E. (2009) Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick? Nat. Rev. Neurosci., 10, 597-609.
    • (2009) Nat. Rev. Neurosci , vol.10 , pp. 597-609
    • Burghes, A.H.1    Beattie, C.E.2
  • 19
    • 84862518720 scopus 로고    scopus 로고
    • Inhibition of apoptosis blocks human motor neuron cell death in a stem cell model of spinal muscular atrophy
    • Sareen, D., Ebert, A.D., Heins, B.M., McGivern, J.V., Ornelas, L. and Svendsen, C.N. (2012) Inhibition of apoptosis blocks human motor neuron cell death in a stem cell model of spinal muscular atrophy. PLoS One, 7, e39113.
    • (2012) PLoS One , vol.7
    • Sareen, D.1    Ebert, A.D.2    Heins, B.M.3    McGivern, J.V.4    Ornelas, L.5    Svendsen, C.N.6
  • 20
    • 84858054407 scopus 로고    scopus 로고
    • Motor neuron rescue in spinal muscular atrophy mice demonstrates that sensorymotor defects are a consequence, not a cause, of motor neuron dysfunction
    • Gogliotti, R.G., Quinlan, K.A., Barlow, C.B., Heier, C.R., Heckman, C.J. and Didonato, C.J. (2012) Motor neuron rescue in spinal muscular atrophy mice demonstrates that sensorymotor defects are a consequence, not a cause, of motor neuron dysfunction. J. Neurosci., 32, 3818-3829.
    • (2012) J. Neurosci , vol.32 , pp. 3818-3829
    • Gogliotti, R.G.1    Quinlan, K.A.2    Barlow, C.B.3    Heier, C.R.4    Heckman, C.J.5    Didonato, C.J.6
  • 22
    • 84884512903 scopus 로고    scopus 로고
    • Improvement of neuromuscular synaptic phenotypes without enhanced survival and motor function in severe spinal muscular atrophy mice selectively rescued in motor neurons
    • Paez-Colasante, X., Seaberg, B., Martinez, T.L., Kong, L., Sumner, C.J. and Rimer, M. (2013) Improvement of neuromuscular synaptic phenotypes without enhanced survival and motor function in severe spinal muscular atrophy mice selectively rescued in motor neurons. PLoS One, 8, e75866.
    • (2013) PLoS One , vol.8
    • Paez-Colasante, X.1    Seaberg, B.2    Martinez, T.L.3    Kong, L.4    Sumner, C.J.5    Rimer, M.6
  • 23
    • 77956603926 scopus 로고    scopus 로고
    • Reduced survival of motor neuron (SMN) protein in motor neuronal progenitors functions cell autonomously to cause spinal muscular atrophy in model mice expressing the human centromeric (SMN2) gene
    • Park, G.H., Maeno-Hikichi, Y., Awano, T., Landmesser, L.T. and Monani, U.R. (2010) Reduced survival of motor neuron (SMN) protein in motor neuronal progenitors functions cell autonomously to cause spinal muscular atrophy in model mice expressing the human centromeric (SMN2) gene. J. Neurosci., 30, 12005-12019.
    • (2010) J. Neurosci , vol.30 , pp. 12005-12019
    • Park, G.H.1    Maeno-Hikichi, Y.2    Awano, T.3    Landmesser, L.T.4    Monani, U.R.5
  • 27
    • 0025811297 scopus 로고
    • Control of embryonic motoneuron survival in vivo by ciliary neurotrophic factor
    • Oppenheim, R.W., Prevette, D., Yin, Q.W., Collins, F. and Mac-Donald, J. (1991) Control of embryonic motoneuron survival in vivo by ciliary neurotrophic factor. Science, 251, 1616-1618.
    • (1991) Science , vol.251 , pp. 1616-1618
    • Oppenheim, R.W.1    Prevette, D.2    Yin, Q.W.3    Collins, F.4    Mac-Donald, J.5
  • 28
    • 0033615957 scopus 로고    scopus 로고
    • Programmed cell death of embryonic motoneurons triggered through the Fas death receptor
    • Raoul, C., Henderson, C.E. and Pettmann, B. (1999) Programmed cell death of embryonic motoneurons triggered through the Fas death receptor. J. Cell. Biol., 147, 1049-1062.
    • (1999) J. Cell. Biol , vol.147 , pp. 1049-1062
    • Raoul, C.1    Henderson, C.E.2    Pettmann, B.3
  • 31
    • 58449137250 scopus 로고    scopus 로고
    • An autopsy case of spinal muscular atrophy type III (Kugelberg-Welander disease)
    • Kuru, S., Sakai, M., Konagaya, M., Yoshida, M., Hashizume, Y. and Saito, K. (2009) An autopsy case of spinal muscular atrophy type III (Kugelberg-Welander disease). Neuropathology, 29, 63-67.
    • (2009) Neuropathology , vol.29 , pp. 63-67
    • Kuru, S.1    Sakai, M.2    Konagaya, M.3    Yoshida, M.4    Hashizume, Y.5    Saito, K.6
  • 32
    • 79957445159 scopus 로고    scopus 로고
    • Defective neuromuscular junction organization and postnatal myogenesis in mice with severe spinal muscular atrophy
    • Dachs, E., Hereu, M., Piedrafita, L., Casanovas, A., Caldero, J. and Esquerda, J.E. (2011) Defective neuromuscular junction organization and postnatal myogenesis in mice with severe spinal muscular atrophy. J. Neuropathol. Exp. Neurol., 70, 444-461.
    • (2011) J. Neuropathol. Exp. Neurol , vol.70 , pp. 444-461
    • Dachs, E.1    Hereu, M.2    Piedrafita, L.3    Casanovas, A.4    Caldero, J.5    Esquerda, J.E.6
  • 33
    • 84880836806 scopus 로고    scopus 로고
    • Spinal muscular atrophy astrocytes exhibit abnormal calcium regulation and reduced growth factor production
    • McGivern, J.V., Patitucci, T.N., Nord, J.A., Barabas, M.E., Stucky, C.L. and Ebert, A.D. (2013) Spinal muscular atrophy astrocytes exhibit abnormal calcium regulation and reduced growth factor production. Glia, 61, 1418-1428.
    • (2013) Glia , vol.61 , pp. 1418-1428
    • McGivern, J.V.1    Patitucci, T.N.2    Nord, J.A.3    Barabas, M.E.4    Stucky, C.L.5    Ebert, A.D.6
  • 34
    • 35549006420 scopus 로고    scopus 로고
    • Glial cells as intrinsic components of non-cell-autonomous neurodegenerative disease
    • Lobsiger, C.S. and Cleveland, D.W. (2007) Glial cells as intrinsic components of non-cell-autonomous neurodegenerative disease. Nat. Neurosci., 10, 1355-1360.
    • (2007) Nat. Neurosci , vol.10 , pp. 1355-1360
    • Lobsiger, C.S.1    Cleveland, D.W.2
  • 38
    • 84859650546 scopus 로고    scopus 로고
    • Partial restoration of cardio-vascular defects in a rescued severe model of spinal muscular atrophy
    • Shababi, M., Habibi, J., Ma, L., Glascock, J.J., Sowers, J.R. and Lorson, C.L. (2012) Partial restoration of cardio-vascular defects in a rescued severe model of spinal muscular atrophy. J. Mol. Cell Cardiol., 52, 1074-1082.
    • (2012) J. Mol. Cell Cardiol , vol.52 , pp. 1074-1082
    • Shababi, M.1    Habibi, J.2    Ma, L.3    Glascock, J.J.4    Sowers, J.R.5    Lorson, C.L.6
  • 39
    • 84874649253 scopus 로고    scopus 로고
    • Recapitulation of spinal motor neuron-specific disease phenotypes in a human cell model of spinal muscular atrophy
    • Wang, Z.B., Zhang, X. and Li, X.J. (2013) Recapitulation of spinal motor neuron-specific disease phenotypes in a human cell model of spinal muscular atrophy. Cell. Res., 23, 378-393.
    • (2013) Cell. Res , vol.23 , pp. 378-393
    • Wang, Z.B.1    Zhang, X.2    Li, X.J.3
  • 42
    • 80055074312 scopus 로고    scopus 로고
    • Astrocytes carrying the superoxide dismutase 1 (SOD1G93A) mutation induce wild-type motor neuron degeneration in vivo
    • Papadeas, S.T., Kraig, S.E., O'Banion, C., Lepore, A.C. and Maragakis, N.J. (2011) Astrocytes carrying the superoxide dismutase 1 (SOD1G93A) mutation induce wild-type motor neuron degeneration in vivo. Proc. Natl Acad. Sci. USA., 108, 17803-17808.
    • (2011) Proc. Natl Acad. Sci. USA , vol.108 , pp. 17803-17808
    • Papadeas, S.T.1    Kraig, S.E.2    O'Banion, C.3    Lepore, A.C.4    Maragakis, N.J.5
  • 44
    • 81855206164 scopus 로고    scopus 로고
    • Brief report: phenotypic rescue of induced pluripotent stem cell-derived motoneurons of a spinal muscular atrophy patient
    • Chang, T., Zheng, W., Tsark, W., Bates, S., Huang, H., Lin, R.J. and Yee, J.K. (2011) Brief report: phenotypic rescue of induced pluripotent stem cell-derived motoneurons of a spinal muscular atrophy patient. Stem Cells, 29, 2090-2093.
    • (2011) Stem Cells , vol.29 , pp. 2090-2093
    • Chang, T.1    Zheng, W.2    Tsark, W.3    Bates, S.4    Huang, H.5    Lin, R.J.6    Yee, J.K.7
  • 47
    • 0027074364 scopus 로고
    • Oxidative DNA damage estimated by 8-hydroxydeoxyguanosine excretion in humans: influence of smoking, gender and body mass index
    • Loft, S., Vistisen, K., Ewertz, M., Tjonneland, A., Overvad, K. and Poulsen, H.E. (1992) Oxidative DNA damage estimated by 8-hydroxydeoxyguanosine excretion in humans: influence of smoking, gender and body mass index. Carcinogenesis, 13, 2241-2247.
    • (1992) Carcinogenesis , vol.13 , pp. 2241-2247
    • Loft, S.1    Vistisen, K.2    Ewertz, M.3    Tjonneland, A.4    Overvad, K.5    Poulsen, H.E.6
  • 48
    • 84867511739 scopus 로고    scopus 로고
    • SMN is required for sensory-motor circuit function in Drosophila
    • Imlach, W.L., Beck, E.S., Choi, B.J., Lotti, F., Pellizzoni, L. and McCabe, B.D. (2012) SMN is required for sensory-motor circuit function in Drosophila. Cell, 151, 427-439.
    • (2012) Cell , vol.151 , pp. 427-439
    • Imlach, W.L.1    Beck, E.S.2    Choi, B.J.3    Lotti, F.4    Pellizzoni, L.5    McCabe, B.D.6
  • 51
    • 33745028132 scopus 로고    scopus 로고
    • The role of mitochondria in inherited neurodegenerative diseases
    • Kwong, J.Q., Beal, M.F. and Manfredi, G. (2006) The role of mitochondria in inherited neurodegenerative diseases. J. Neurochem., 97, 1659-1675.
    • (2006) J. Neurochem , vol.97 , pp. 1659-1675
    • Kwong, J.Q.1    Beal, M.F.2    Manfredi, G.3
  • 52
    • 84904648362 scopus 로고    scopus 로고
    • Mitochondria-targeted catalase reverts the neurotoxicity of hSOD1G(9)(3)A astrocytes without extending the survival of ALS-linked mutant hSOD1 mice
    • Pehar, M., Beeson, G., Beeson, C.C., Johnson, J.A. and Vargas, M. R. (2014) Mitochondria-targeted catalase reverts the neurotoxicity of hSOD1G(9)(3)A astrocytes without extending the survival of ALS-linked mutant hSOD1 mice. PLoS One, 9, e103438.
    • (2014) PLoS One , vol.9
    • Pehar, M.1    Beeson, G.2    Beeson, C.C.3    Johnson, J.A.4    Vargas, M.R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.