메뉴 건너뛰기




Volumn 49, Issue 7, 2006, Pages 651-664

Spastin in the human and mouse central nervous system with special reference to its expression in the hippocampus of mouse pilocarpine model of status epilepticus and temporal lobe epilepsy

Author keywords

Central nervous system; Distribution; Epilepsy; Hippocampus; Human; Mouse; Spastin

Indexed keywords

MESSENGER RNA; PILOCARPINE; SPASTIN;

EID: 33750012332     PISSN: 01970186     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuint.2006.05.008     Document Type: Article
Times cited : (12)

References (36)
  • 1
    • 0015113564 scopus 로고
    • Familial spastic paraplegia (a review with four case reports)
    • Arjundas G., Ramamurthi B., and Chettur L. Familial spastic paraplegia (a review with four case reports). J. Assoc. Phys. India 19 (1971) 653-657
    • (1971) J. Assoc. Phys. India , vol.19 , pp. 653-657
    • Arjundas, G.1    Ramamurthi, B.2    Chettur, L.3
  • 3
    • 0041550246 scopus 로고
    • The association of familial spastic paraplegia and epilepsy in one family
    • Bruyn G.W., and Mechelse K. The association of familial spastic paraplegia and epilepsy in one family. Psychiatr. Neurol. Neurochir. 65 (1962) 280-292
    • (1962) Psychiatr. Neurol. Neurochir. , vol.65 , pp. 280-292
    • Bruyn, G.W.1    Mechelse, K.2
  • 4
    • 0025134468 scopus 로고
    • Cortical neurons expressing the cholecystokinin gene in the rat: distribution in the adult brain, ontogeny, and some of their projections
    • Burgunder J.M., and Young III W.S. Cortical neurons expressing the cholecystokinin gene in the rat: distribution in the adult brain, ontogeny, and some of their projections. J. Comp. Neurol. 300 (1990) 26-46
    • (1990) J. Comp. Neurol. , vol.300 , pp. 26-46
    • Burgunder, J.M.1    Young III, W.S.2
  • 5
    • 0037231374 scopus 로고    scopus 로고
    • Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus
    • Charvin D., Cifuentes-Diaz C., Fonknechten N., Joshi V., Hazan J., Melki J., and Betuing S. Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus. Hum. Mol. Genet. 12 (2003) 71-78
    • (2003) Hum. Mol. Genet. , vol.12 , pp. 71-78
    • Charvin, D.1    Cifuentes-Diaz, C.2    Fonknechten, N.3    Joshi, V.4    Hazan, J.5    Melki, J.6    Betuing, S.7
  • 6
    • 24944560482 scopus 로고    scopus 로고
    • Spastin subcellular localization is regulated through usage of different translation start sites and active export from the nucleus
    • Claudiani P., Riano E., Errico A., Andolfi G., and Rugarli E.I. Spastin subcellular localization is regulated through usage of different translation start sites and active export from the nucleus. Exp. Cell Res. 309 (2005) 358-369
    • (2005) Exp. Cell Res. , vol.309 , pp. 358-369
    • Claudiani, P.1    Riano, E.2    Errico, A.3    Andolfi, G.4    Rugarli, E.I.5
  • 7
    • 0037081740 scopus 로고    scopus 로고
    • Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics
    • Errico A., Ballabio A., and Rugarli E.I. Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics. Hum. Mol. Genet. 11 (2002) 153-163
    • (2002) Hum. Mol. Genet. , vol.11 , pp. 153-163
    • Errico, A.1    Ballabio, A.2    Rugarli, E.I.3
  • 8
    • 5744240094 scopus 로고    scopus 로고
    • Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axon
    • Errico A., Claudiani P., D'Addio M., and Rugarli E.I. Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axon. Hum. Mol. Genet. 13 (2004) 2121-2132
    • (2004) Hum. Mol. Genet. , vol.13 , pp. 2121-2132
    • Errico, A.1    Claudiani, P.2    D'Addio, M.3    Rugarli, E.I.4
  • 9
    • 13944283245 scopus 로고    scopus 로고
    • Linking axonal degeneration to microtubule remodeling by spastin-mediated microtubule severing
    • Evans K.J., Gomes E.R., Reisenweber S.M., Gundersen G.G., and Lauring B.P. Linking axonal degeneration to microtubule remodeling by spastin-mediated microtubule severing. J. Cell Biol. 168 (2005) 599-606
    • (2005) J. Cell Biol. , vol.168 , pp. 599-606
    • Evans, K.J.1    Gomes, E.R.2    Reisenweber, S.M.3    Gundersen, G.G.4    Lauring, B.P.5
  • 10
    • 0036267195 scopus 로고    scopus 로고
    • Hereditary spastic paraplegia: the pace quickens
    • Fink J.K. Hereditary spastic paraplegia: the pace quickens. Ann. Neurol. 51 (2002) 669-672
    • (2002) Ann. Neurol. , vol.51 , pp. 669-672
    • Fink, J.K.1
  • 16
    • 0035208727 scopus 로고    scopus 로고
    • A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members
    • Mead S.H., Proukakis C., Wood N., Crosby A.H., Plant G.T., and Warner T.T. A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members. J. Neurol. Neurosurg. Psychiatry 71 (2001) 788-791
    • (2001) J. Neurol. Neurosurg. Psychiatry , vol.71 , pp. 788-791
    • Mead, S.H.1    Proukakis, C.2    Wood, N.3    Crosby, A.H.4    Plant, G.T.5    Warner, T.T.6
  • 17
    • 0032969563 scopus 로고    scopus 로고
    • AAA+: a class of chaperone-like ATPases associated with the assembly, operation, and disassembly of protein complexes
    • Neuwald A.F., Aravind L., Spouge J.L., and Koonin E.V. AAA+: a class of chaperone-like ATPases associated with the assembly, operation, and disassembly of protein complexes. Genome Res. 9 (1999) 27-43
    • (1999) Genome Res. , vol.9 , pp. 27-43
    • Neuwald, A.F.1    Aravind, L.2    Spouge, J.L.3    Koonin, E.V.4
  • 19
    • 0034773892 scopus 로고    scopus 로고
    • Autopsy case of autosomal recessive hereditary spastic paraplegia with reference to the muscular pathology
    • Nomura H., Koike F., Tsuruta Y., Iwaki A., and Iwaki T. Autopsy case of autosomal recessive hereditary spastic paraplegia with reference to the muscular pathology. Neuropathology 21 (2001) 212-217
    • (2001) Neuropathology , vol.21 , pp. 212-217
    • Nomura, H.1    Koike, F.2    Tsuruta, Y.3    Iwaki, A.4    Iwaki, T.5
  • 20
    • 0033845095 scopus 로고    scopus 로고
    • Neurological and neuroradiological progression in hereditary spastic paraplegia with a thin corpus callosum
    • Okubo S., Ueda M., Kamiya T., Mizumura S., Terashi A., and Katayama Y. Neurological and neuroradiological progression in hereditary spastic paraplegia with a thin corpus callosum. Acta Neurol. Scand. 102 (2000) 196-199
    • (2000) Acta Neurol. Scand. , vol.102 , pp. 196-199
    • Okubo, S.1    Ueda, M.2    Kamiya, T.3    Mizumura, S.4    Terashi, A.5    Katayama, Y.6
  • 21
    • 0031973716 scopus 로고    scopus 로고
    • The AAA team: related ATPases with diverse functions
    • Patel S., and Latterich M. The AAA team: related ATPases with diverse functions. Trends Cell Biol. 8 (1998) 65-71
    • (1998) Trends Cell Biol. , vol.8 , pp. 65-71
    • Patel, S.1    Latterich, M.2
  • 23
    • 12344250580 scopus 로고    scopus 로고
    • The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B
    • Reid E., Connell J., Edwards T.L., Duley S., Brown S.E., and Sanderson C.M. The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B. Hum. Mol. Genet. 14 (2005) 19-38
    • (2005) Hum. Mol. Genet. , vol.14 , pp. 19-38
    • Reid, E.1    Connell, J.2    Edwards, T.L.3    Duley, S.4    Brown, S.E.5    Sanderson, C.M.6
  • 24
    • 0016173785 scopus 로고
    • Hereditary spastic paraplegia in western Norway
    • Skre H. Hereditary spastic paraplegia in western Norway. Clin. Genet. 6 (1974) 165-183
    • (1974) Clin. Genet. , vol.6 , pp. 165-183
    • Skre, H.1
  • 25
    • 0025885121 scopus 로고
    • Hereditary spastic paraplegia with epileptic myoclonus
    • Sommerfelt K., Kyllerman M., and Sanner G. Hereditary spastic paraplegia with epileptic myoclonus. Acta Neurol. Scand. 84 (1991) 157-160
    • (1991) Acta Neurol. Scand. , vol.84 , pp. 157-160
    • Sommerfelt, K.1    Kyllerman, M.2    Sanner, G.3
  • 26
    • 0001432872 scopus 로고
    • Beitrage zur Pathologie des Ruckenmarks
    • Strmpell A. Beitrage zur Pathologie des Ruckenmarks. Arch. Psychiatr. Nervenkr. 10 (1880) 676-717
    • (1880) Arch. Psychiatr. Nervenkr. , vol.10 , pp. 676-717
    • Strmpell, A.1
  • 29
    • 4344633672 scopus 로고    scopus 로고
    • Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese cases
    • Tang B.S., Chen X., Zhao G.H., Shen L., Yan X.X., Jiang H., and Luo W. Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese cases. Chin. Med. J. (Engl.) 117 (2004) 1002-1005
    • (2004) Chin. Med. J. (Engl.) , vol.117 , pp. 1002-1005
    • Tang, B.S.1    Chen, X.2    Zhao, G.H.3    Shen, L.4    Yan, X.X.5    Jiang, H.6    Luo, W.7
  • 30
    • 3042731113 scopus 로고    scopus 로고
    • Metabotropic glutamate receptor2/3 in the hippocampus of patients with mesial temporal lobe epilepsy, of rats and mice after pilocarpine-induced status epilepticus
    • Tang F.R., Chia S.C., Chen P.M., Gao H., Lee W.L., Yeo T.S., Burgunder J.M., Probst A., Sim M.K., and Ling E.A. Metabotropic glutamate receptor2/3 in the hippocampus of patients with mesial temporal lobe epilepsy, of rats and mice after pilocarpine-induced status epilepticus. Epilepsy Res. 59 (2004) 167-180
    • (2004) Epilepsy Res. , vol.59 , pp. 167-180
    • Tang, F.R.1    Chia, S.C.2    Chen, P.M.3    Gao, H.4    Lee, W.L.5    Yeo, T.S.6    Burgunder, J.M.7    Probst, A.8    Sim, M.K.9    Ling, E.A.10
  • 31
    • 20444451699 scopus 로고    scopus 로고
    • Glutamate receptor 1 immunopositive neurons in the gliotic CA1 area of the mouse hippocampus after pilocarpine induced status epilepticus
    • Tang F.R., Chia S.C., Zhang S., Chen P.M., Gao H., Liu C.P., Khanna S., and Lee W.L. Glutamate receptor 1 immunopositive neurons in the gliotic CA1 area of the mouse hippocampus after pilocarpine induced status epilepticus. Eur. J. Neursci. 21 (2005) 2361-2374
    • (2005) Eur. J. Neursci. , vol.21 , pp. 2361-2374
    • Tang, F.R.1    Chia, S.C.2    Zhang, S.3    Chen, P.M.4    Gao, H.5    Liu, C.P.6    Khanna, S.7    Lee, W.L.8
  • 32
    • 1542395710 scopus 로고    scopus 로고
    • Expression of different isoforms of protein kinase C in the rat hippocampus after pilocarpine induced status epilepticus with special reference to CA1 area and the dentate gyrus
    • Tang F.R., Lee W.L., Gao H., Chen Y., Loh Y.T., and Chia S.C. Expression of different isoforms of protein kinase C in the rat hippocampus after pilocarpine induced status epilepticus with special reference to CA1 area and the dentate gyrus. Hippocampus 14 (2004) 87-98
    • (2004) Hippocampus , vol.14 , pp. 87-98
    • Tang, F.R.1    Lee, W.L.2    Gao, H.3    Chen, Y.4    Loh, Y.T.5    Chia, S.C.6
  • 33
    • 0030987023 scopus 로고    scopus 로고
    • A family with hereditary spastic paraparesis and epilepsy
    • Webb S., Flanagan N., Callaghan N., and Hutchinson M. A family with hereditary spastic paraparesis and epilepsy. Epilepsia 38 (1997) 495-499
    • (1997) Epilepsia , vol.38 , pp. 495-499
    • Webb, S.1    Flanagan, N.2    Callaghan, N.3    Hutchinson, M.4
  • 36
    • 0027264723 scopus 로고
    • Hereditary spastic paraplegia associated with epilepsy, mental retardation and hearing impairment
    • Yih J.S., Wang S.J., Su M.S., Tsai S.C., Lin R.H., Lin K.N., and Liu H.C. Hereditary spastic paraplegia associated with epilepsy, mental retardation and hearing impairment. Paraplegia 31 (1993) 408-411
    • (1993) Paraplegia , vol.31 , pp. 408-411
    • Yih, J.S.1    Wang, S.J.2    Su, M.S.3    Tsai, S.C.4    Lin, R.H.5    Lin, K.N.6    Liu, H.C.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.