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Volumn 394, Issue 4, 1998, Pages 506-519

Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene

Author keywords

Axonal degeneration; Demyelination; Pelizaeus Merzbacher disease

Indexed keywords

PROTEOLIPID;

EID: 0032543261     PISSN: 00219967     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-9861(19980518)394:4<506::AID-CNE8>3.0.CO;2-5     Document Type: Article
Times cited : (121)

References (62)
  • 1
    • 0020489908 scopus 로고
    • Cloning and characterisation of the abundant cytoplasmic 7S RNA from mouse cells
    • Balmain, A., R. Krumlauf, J.K. Vass, and G.D. Birnie (1982) Cloning and characterisation of the abundant cytoplasmic 7S RNA from mouse cells. Nucleic Acids Res. 10:4259-4277.
    • (1982) Nucleic Acids Res. , vol.10 , pp. 4259-4277
    • Balmain, A.1    Krumlauf, R.2    Vass, J.K.3    Birnie, G.D.4
  • 4
    • 0028293176 scopus 로고
    • Morphological changes in oligodendrocytes in the intact mouse optic nerve following intravitreal injection of tumour necrosis factor
    • Butt, A.M. and H.G. Jenkins (1994) Morphological changes in oligodendrocytes in the intact mouse optic nerve following intravitreal injection of tumour necrosis factor. J. Neuroimmunol. 51:27-33.
    • (1994) J. Neuroimmunol. , vol.51 , pp. 27-33
    • Butt, A.M.1    Jenkins, H.G.2
  • 5
    • 0029919187 scopus 로고    scopus 로고
    • Macrophage microglial-mediated primary demyelination and motor disease induced by the central nervous system production of interleukin-3 in transgenic mice
    • Chiang, C.S., H.C. Powell, L.H. Gold, A. Samimi, and I.L. Campbell (1996) Macrophage microglial-mediated primary demyelination and motor disease induced by the central nervous system production of interleukin-3 in transgenic mice. J. Clin. Invest. 97:1512-1524.
    • (1996) J. Clin. Invest. , vol.97 , pp. 1512-1524
    • Chiang, C.S.1    Powell, H.C.2    Gold, L.H.3    Samimi, A.4    Campbell, I.L.5
  • 6
    • 0030602822 scopus 로고    scopus 로고
    • Myelination in the absence of galactocerebroside and sulfatide: Normal structure with abnormal function and regional instability
    • Coetzee, T., N. Fujita, J. Dupree, R. Shi, A. Blight, K. Suzuki, and B. Popko (1996) Myelination in the absence of galactocerebroside and sulfatide: Normal structure with abnormal function and regional instability. Cell 86:209-213.
    • (1996) Cell , vol.86 , pp. 209-213
    • Coetzee, T.1    Fujita, N.2    Dupree, J.3    Shi, R.4    Blight, A.5    Suzuki, K.6    Popko, B.7
  • 7
    • 0023493525 scopus 로고
    • An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region
    • Cremers, F.P.M., R.A. Pfeiffer, T.J.R. van de Pol, M.H. Hofker, T.A. Kruse, B. Wieringa, and H.H. Ropers (1987) An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region. Hum. Genet. 77:23-27.
    • (1987) Hum. Genet. , vol.77 , pp. 23-27
    • Cremers, F.P.M.1    Pfeiffer, R.A.2    Van De Pol, T.J.R.3    Hofker, M.H.4    Kruse, T.A.5    Wieringa, B.6    Ropers, H.H.7
  • 8
    • 0025949638 scopus 로고
    • Local control of axonal properties by Schwann cells: Neurofilaments and axonal transport in homologous and heterologous nerve grafts
    • De Waegh, S.M. and S.T. Brady (1991) Local control of axonal properties by Schwann cells: Neurofilaments and axonal transport in homologous and heterologous nerve grafts. J. Neurosci. Res. 30:201-212.
    • (1991) J. Neurosci. Res. , vol.30 , pp. 201-212
    • De Waegh, S.M.1    Brady, S.T.2
  • 9
    • 0026580004 scopus 로고
    • Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells
    • De Waegh, S.M., V.M.Y. Lee, and S.T. Brady (1992) Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells. Cell 68:451-463.
    • (1992) Cell , vol.68 , pp. 451-463
    • De Waegh, S.M.1    Lee, V.M.Y.2    Brady, S.T.3
  • 10
    • 0019975488 scopus 로고
    • Ultrastructure of the central nervous system in a myelin deficient rat
    • Dentinger, M.P., K.D. Barron, and C.K. Csiza (1982) Ultrastructure of the central nervous system in a myelin deficient rat. J. Neurocytol. 11:671-691.
    • (1982) J. Neurocytol. , vol.11 , pp. 671-691
    • Dentinger, M.P.1    Barron, K.D.2    Csiza, C.K.3
  • 11
    • 0023404814 scopus 로고
    • Abnormal compact myelin in the myelin-deficient rat: Absence of proteolipid protein correlates with a defect in the intraperiod line
    • Duncan, I.D., J.P. Hammang, and B.D. Trapp (1987) Abnormal compact myelin in the myelin-deficient rat: Absence of proteolipid protein correlates with a defect in the intraperiod line. Proc. Natl. Acad. Sci. USA 84:6287-6291.
    • (1987) Proc. Natl. Acad. Sci. USA , vol.84 , pp. 6287-6291
    • Duncan, I.D.1    Hammang, J.P.2    Trapp, B.D.3
  • 12
    • 0028240173 scopus 로고
    • Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease
    • Ellis, D. and S. Malcolm (1994) Proteolipid protein gene dosage effect in Pelizaeus-Merzbacher disease. Nature Genet. 6:333-334.
    • (1994) Nature Genet. , vol.6 , pp. 333-334
    • Ellis, D.1    Malcolm, S.2
  • 13
    • 0026493451 scopus 로고
    • Rumpshaker: An X-linked mutation causing hypomyelination. Developmental differences in myelination and glial cells between the optic nerve and spinal cord
    • Fanarraga, M.L., I.R. Griffiths, M.C. McCulloch, J.A. Barrie, P.G.E. Kennedy, and P.J. Brophy (1992) Rumpshaker: An X-linked mutation causing hypomyelination. Developmental differences in myelination and glial cells between the optic nerve and spinal cord. Glia 5:161-170.
    • (1992) Glia , vol.5 , pp. 161-170
    • Fanarraga, M.L.1    Griffiths, I.R.2    McCulloch, M.C.3    Barrie, J.A.4    Kennedy, P.G.E.5    Brophy, P.J.6
  • 14
    • 0029076362 scopus 로고
    • Microglia: Intrinsic immuneffector cell of the brain
    • Gehrmann, J., Y. Matsumoto, and G.W. Kreutzberg (1995) Microglia: Intrinsic immuneffector cell of the brain. Brain Res. Rev. 20:269-287.
    • (1995) Brain Res. Rev. , vol.20 , pp. 269-287
    • Gehrmann, J.1    Matsumoto, Y.2    Kreutzberg, G.W.3
  • 15
    • 0026615047 scopus 로고
    • 0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons
    • 0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons. Cell 71:565-576.
    • (1992) Cell , vol.71 , pp. 565-576
    • Giese, K.P.1    Martini, R.2    Lemke, G.3    Soriano, P.4    Schachner, M.5
  • 17
    • 0030174240 scopus 로고    scopus 로고
    • Overexpression of 2′,3′-cyclic nucleotide 3′-phosphodiesterase in transgenic mice alters oligodendrocyte development and produces aberrant myelination
    • Gravel, M., J. Peterson, V.W. Yong, V. Kottis, B. Trapp, and P.E. Braun (1996) Overexpression of 2′,3′-cyclic nucleotide 3′-phosphodiesterase in transgenic mice alters oligodendrocyte development and produces aberrant myelination. Mol. Cell. Neurosci. 7:453-466.
    • (1996) Mol. Cell. Neurosci. , vol.7 , pp. 453-466
    • Gravel, M.1    Peterson, J.2    Yong, V.W.3    Kottis, V.4    Trapp, B.5    Braun, P.E.6
  • 18
    • 0030271561 scopus 로고    scopus 로고
    • Myelin mutants: Model systems to study normal and abnormal myelination
    • Griffiths, I.R. (1996) Myelin mutants: Model systems to study normal and abnormal myelination. Bioessays 18:789-797.
    • (1996) Bioessays , vol.18 , pp. 789-797
    • Griffiths, I.R.1
  • 20
    • 0025231337 scopus 로고
    • Rumpshaker mouse: A new X-linked mutation affecting myelination: Evidence for a defect in PLP expression
    • Griffiths, I.R., I. Scott, M.C. McCulloch, J.A, Barrie, K. McPhilemy, and B.M. Cattanach (1990) Rumpshaker mouse: A new X-linked mutation affecting myelination: Evidence for a defect in PLP expression. J. Neurocytol. 19:273-283.
    • (1990) J. Neurocytol. , vol.19 , pp. 273-283
    • Griffiths, I.R.1    Scott, I.2    McCulloch, M.C.3    Barrie, J.A.4    McPhilemy, K.5    Cattanach, B.M.6
  • 21
    • 0029080438 scopus 로고
    • Transgenic and natural mouse models of proteolipid protein (PLP) related dysmyelination and demyelination
    • Griffiths, I.R., A. Schneider, J. Anderson, and K.-A. Nave (1995) Transgenic and natural mouse models of proteolipid protein (PLP) related dysmyelination and demyelination. Brain Pathol. 5:275-281.
    • (1995) Brain Pathol. , vol.5 , pp. 275-281
    • Griffiths, I.R.1    Schneider, A.2    Anderson, J.3    Nave, K.-A.4
  • 23
    • 0006283636 scopus 로고
    • Development and maturation of central nervous system myelin: Comparison of immunohistochemical localization of proteolipid protein and basic protein in myelin and oligodendrocytes
    • Hartman, B.K., H.C. Agrawal, D. Agrawal, and S. Kalmbach (1982) Development and maturation of central nervous system myelin: Comparison of immunohistochemical localization of proteolipid protein and basic protein in myelin and oligodendrocytes. Proc. Natl. Acad. Sci. USA 79:4217-4220.
    • (1982) Proc. Natl. Acad. Sci. USA , vol.79 , pp. 4217-4220
    • Hartman, B.K.1    Agrawal, H.C.2    Agrawal, D.3    Kalmbach, S.4
  • 24
    • 0015165838 scopus 로고
    • Ultrastructural and light-microscopic studies of the developing feline spinal cord white matter. I. the nodes of Ranvier
    • Hildebrand, C. (1971) Ultrastructural and light-microscopic studies of the developing feline spinal cord white matter. I. The nodes of Ranvier. Acta Physiol. Scand. 364(Suppl.):81-108.
    • (1971) Acta Physiol. Scand. , vol.364 , Issue.SUPPL. , pp. 81-108
    • Hildebrand, C.1
  • 26
    • 0029980997 scopus 로고    scopus 로고
    • The proteolipid protein gene: Double, double, . . . and trouble
    • Hodes, M.E. and S.R. Dlouhy (1996) The proteolipid protein gene: Double, double, . . . and trouble. Am. J. Hum. Genet. 59:12-15.
    • (1996) Am. J. Hum. Genet. , vol.59 , pp. 12-15
    • Hodes, M.E.1    Dlouhy, S.R.2
  • 27
    • 0027759985 scopus 로고
    • Genetics of Pelizaeus-Merzbacher disease
    • Hodes, M.E., V.M. Pratt, and S.R. Dlouhy (1993) Genetics of Pelizaeus-Merzbacher disease. Dev. Neurosci. 15:383-394.
    • (1993) Dev. Neurosci. , vol.15 , pp. 383-394
    • Hodes, M.E.1    Pratt, V.M.2    Dlouhy, S.R.3
  • 30
    • 0030176138 scopus 로고    scopus 로고
    • Cell death of oligodendrocytes or demyelination induced by overexpression of proteolipid protein depending on expressed gene dosage
    • Inoue, Y., T. Kagawa, Y. Matsumura, K. Ikenaka, and K. Mikoshiba (1996) Cell death of oligodendrocytes or demyelination induced by overexpression of proteolipid protein depending on expressed gene dosage. Neurosci. Res. 25:161-172.
    • (1996) Neurosci. Res. , vol.25 , pp. 161-172
    • Inoue, Y.1    Kagawa, T.2    Matsumura, Y.3    Ikenaka, K.4    Mikoshiba, K.5
  • 31
    • 0028893387 scopus 로고
    • Over-expression of the DM-20 myelin proteolipid causes central nervous system demyelination in transgenic mice
    • Johnson, R.S., J.C. Roder, and J.R. Riordan (1995) Over-expression of the DM-20 myelin proteolipid causes central nervous system demyelination in transgenic mice. J. Neurochem. 64:967-976.
    • (1995) J. Neurochem. , vol.64 , pp. 967-976
    • Johnson, R.S.1    Roder, J.C.2    Riordan, J.R.3
  • 32
    • 0002397825 scopus 로고
    • A sex-linked recessive form of spastic paraplegia
    • Johnston, A.W. and V.A. McKusick (1962) A sex-linked recessive form of spastic paraplegia. Am. J. Hum. Genet. 14:83-94.
    • (1962) Am. J. Hum. Genet. , vol.14 , pp. 83-94
    • Johnston, A.W.1    McKusick, V.A.2
  • 35
    • 0028143554 scopus 로고
    • Modulation of the axonal microtubule cytoskeleton by myelinating Schwann cells
    • Kirkpatrick, L.L. and S.T. Brady (1994) Modulation of the axonal microtubule cytoskeleton by myelinating Schwann cells. J. Neurosci. 14:7440-7450.
    • (1994) J. Neurosci. , vol.14 , pp. 7440-7450
    • Kirkpatrick, L.L.1    Brady, S.T.2
  • 37
    • 0028236505 scopus 로고
    • The rumpshaker mutation in spastic paraplegia
    • Kobayashi, H., E.P. Hoffman, and H.G. Marks (1994) The rumpshaker mutation in spastic paraplegia. Nature Genet. 7:351-352.
    • (1994) Nature Genet. , vol.7 , pp. 351-352
    • Kobayashi, H.1    Hoffman, E.P.2    Marks, H.G.3
  • 38
    • 0029982692 scopus 로고    scopus 로고
    • Molecular genetics of familial spastic paraplegia: A multitude of responsible genes
    • Kobayashi, H., C.A. Garcia, G. Alfonso, H.G. Marks, and E.P. Hoffman (1996) Molecular genetics of familial spastic paraplegia: A multitude of responsible genes. J. Neurol. Sci. 137:131-138.
    • (1996) J. Neurol. Sci. , vol.137 , pp. 131-138
    • Kobayashi, H.1    Garcia, C.A.2    Alfonso, G.3    Marks, H.G.4    Hoffman, E.P.5
  • 39
    • 0023153460 scopus 로고
    • Defective biosynthesis of proteolipid protein in Pelizaeus-Merzbacher disease
    • Koeppen, A.H., N.A. Ronca, E.A. Greenfield, and M.B. Hans (1987) Defective biosynthesis of proteolipid protein in Pelizaeus-Merzbacher disease. Ann. Neurol. 21:159-170.
    • (1987) Ann. Neurol. , vol.21 , pp. 159-170
    • Koeppen, A.H.1    Ronca, N.A.2    Greenfield, E.A.3    Hans, M.B.4
  • 40
    • 0031081587 scopus 로고    scopus 로고
    • Dying-back oligodendrogliopathy: A late sequel of myelin-associated glycoprotein deficiency
    • Lassmann, H., U. Bartsch, D. Montag, and M. Schachner (1997) Dying-back oligodendrogliopathy: A late sequel of myelin-associated glycoprotein deficiency. Glia 19:104-110.
    • (1997) Glia , vol.19 , pp. 104-110
    • Lassmann, H.1    Bartsch, U.2    Montag, D.3    Schachner, M.4
  • 41
    • 0000029565 scopus 로고
    • Proteins of myelin
    • P. Morell (ed): New York: Plenum Press
    • Lees, M.B. and S.W. Brostoff (1984) Proteins of myelin. In P. Morell (ed): Myelin. New York: Plenum Press, pp. 197-224.
    • (1984) Myelin , pp. 197-224
    • Lees, M.B.1    Brostoff, S.W.2
  • 42
    • 0007208587 scopus 로고
    • Diffuse sclerosis with preserved myelin islands
    • Löwenberg, K. and T.S. Hill (1933) Diffuse sclerosis with preserved myelin islands. Arch. Neurol. Psychiatr. 29:1232-1245.
    • (1933) Arch. Neurol. Psychiatr. , vol.29 , pp. 1232-1245
    • Löwenberg, K.1    Hill, T.S.2
  • 43
    • 0030773792 scopus 로고    scopus 로고
    • The pathobiology of the oligodendrocyte
    • Ludwin, S.K. (1997) The pathobiology of the oligodendrocyte. J. Neuropathol. Exp. Neurol. 56:111-124.
    • (1997) J. Neuropathol. Exp. Neurol. , vol.56 , pp. 111-124
    • Ludwin, S.K.1
  • 46
    • 0016335085 scopus 로고
    • Periodate-lysine-paraformaldehyde fixative. A new fixation for immunoeleetron microscopy
    • McLean, I.W. and P.K. Nakane (1974) Periodate-lysine-paraformaldehyde fixative. A new fixation for immunoeleetron microscopy. J. Histochem. Cytochem. 12:1077-1083.
    • (1974) J. Histochem. Cytochem. , vol.12 , pp. 1077-1083
    • McLean, I.W.1    Nakane, P.K.2
  • 47
    • 0022133330 scopus 로고
    • Nucleotide sequence of two mRNAs for rat brain myelin proteolipid protein
    • Milner, R.J., C. Lai, K.-A. Nave, D. Lenoir, J. Ogata, and J.G. Sutcliffe (1985) Nucleotide sequence of two mRNAs for rat brain myelin proteolipid protein. Cell 42:931-939.
    • (1985) Cell , vol.42 , pp. 931-939
    • Milner, R.J.1    Lai, C.2    Nave, K.-A.3    Lenoir, D.4    Ogata, J.5    Sutcliffe, J.G.6
  • 50
    • 0029960739 scopus 로고    scopus 로고
    • Adult-onset neurodegenerative disorder due to proteolipid protein gene mutation in the mother of a man with Pelizaeus-Merzbacher disease
    • Nance, M.A., S. Boyadjiev, V.M. Pratt, S. Taylor, M.E. Hodes, and S.R. Dlouhy (1996) Adult-onset neurodegenerative disorder due to proteolipid protein gene mutation in the mother of a man with Pelizaeus-Merzbacher disease. Neurology 47:1333-1335.
    • (1996) Neurology , vol.47 , pp. 1333-1335
    • Nance, M.A.1    Boyadjiev, S.2    Pratt, V.M.3    Taylor, S.4    Hodes, M.E.5    Dlouhy, S.R.6
  • 51
    • 0005457564 scopus 로고    scopus 로고
    • Myelin-specific genes and their mutations in the mouse
    • K.R. Jessen and W.D. Richardson (eds): Oxford: Bios
    • Nave, K.-A. (1996) Myelin-specific genes and their mutations in the mouse. In K.R. Jessen and W.D. Richardson (eds): Glial Cell Development. Basic Principles and Clinical Relevance. Oxford: Bios, pp. 141-164.
    • (1996) Glial Cell Development. Basic Principles and Clinical Relevance , pp. 141-164
    • Nave, K.-A.1
  • 52
    • 0002768920 scopus 로고    scopus 로고
    • X-linked developmental defects in myelination: From mouse mutants to human genetic diseases
    • Nave, K.-A. and O. Boespflug-Tanguy (1996) X-linked developmental defects in myelination: From mouse mutants to human genetic diseases. Neuroscientist 2:33-43.
    • (1996) Neuroscientist , vol.2 , pp. 33-43
    • Nave, K.-A.1    Boespflug-Tanguy, O.2
  • 53
    • 0028864801 scopus 로고
    • Spontaneous inflammatory demyelinating disease in transgenic mice showing central nervous system-specific expression of tumor necrosis factor α
    • Probert, L., K. Akassoglou, M. Pasparakis, G. Kontogeorgos, and G. Kollias (1995) Spontaneous inflammatory demyelinating disease in transgenic mice showing central nervous system-specific expression of tumor necrosis factor α. Proc. Natl. Acad. Sci. USA 92:11294-11298.
    • (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 11294-11298
    • Probert, L.1    Akassoglou, K.2    Pasparakis, M.3    Kontogeorgos, G.4    Kollias, G.5
  • 54
    • 0026348463 scopus 로고
    • Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease
    • Raskind, W.H., C.A. Williams, L.D. Hudson, and T.D. Bird (1991) Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease. Am. J. Hum. Genet. 49:1355-1360.
    • (1991) Am. J. Hum. Genet. , vol.49 , pp. 1355-1360
    • Raskind, W.H.1    Williams, C.A.2    Hudson, L.D.3    Bird, T.D.4
  • 55
    • 0028325902 scopus 로고
    • Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage
    • Readhead, C., A. Schneider, I.R. Griffiths, and K.-A. Nave (1994) Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage. Neuron 12:583-595.
    • (1994) Neuron , vol.12 , pp. 583-595
    • Readhead, C.1    Schneider, A.2    Griffiths, I.R.3    Nave, K.-A.4
  • 56
  • 57
    • 0029145584 scopus 로고
    • Neuropathology and genetics of Pelizaeus-Merzbacher disease
    • Seitelberger, F. (1995) Neuropathology and genetics of Pelizaeus-Merzbacher disease. Brain Pathol. 5:267-273.
    • (1995) Brain Pathol. , vol.5 , pp. 267-273
    • Seitelberger, F.1
  • 60
    • 0345542549 scopus 로고    scopus 로고
    • Duplication of the proteolipid protein gene (PLP) is a frequent cause of Pelizaeus Merzbacher disease
    • Sistermans, E.A., I.J. De Wijs, I.F.M. De Coo, and B.A. Van Oost (1996) Duplication of the proteolipid protein gene (PLP) is a frequent cause of Pelizaeus Merzbacher disease [abstract]. Am. J. Hum. Genet. 10:A10.
    • (1996) Am. J. Hum. Genet. , vol.10
    • Sistermans, E.A.1    De Wijs, I.J.2    De Coo, I.F.M.3    Van Oost, B.A.4
  • 61
    • 0029093622 scopus 로고
    • Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models
    • Snipes, G.J. and U. Suter (1995) Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models. Brain Pathol. 5:233-247.
    • (1995) Brain Pathol. , vol.5 , pp. 233-247
    • Snipes, G.J.1    Suter, U.2


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