Contacts cellulaires des fibres myélinisées du système nerveux périphérique

Ksénia Oguievetskaia; Carmen Cifuentes-Diaz; Jean-Antoine Girault; Laurence Goutebroze

doi:10.1051/medsci/2005212162

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Volume 21 / No 2 (Février 2005)

Med Sci (Paris), 21 2 (2005) 162-169

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Issue		Med Sci (Paris) Volume 21, Number 2, Février 2005


Page(s)		162 - 169
Section		M/S revues
DOI		https://doi.org/10.1051/medsci/2005212162
Published online		15 February 2005

Arroyo EJ, Scherer SS. On the molecular architecture of myelinated fibers. Histochem Cell Biol 2000; 113 : 1–18. [Google Scholar]
Filbin MT, Tennekoon GI. The role of complex carbohydrates in adhesion of the myelin protein, P0. Neuron 1991; 7 : 845–55. [Google Scholar]
Tetzlaff W. Tight junction contact events and temporary gap junctions in the sciatic nerve fibres of the chicken during Wallerian degeneration and subsequent regeneration. J Neurocytol 1982; 11 : 839–58. [Google Scholar]
Fannon AM, Sherman DL, Ilyina-Gragerova G, et al. Novel E-cadherin-mediated adhesion in peripheral nerve : Schwann cell architecture is stabilized by autotypic adherens junctions. J Cell Biol 1995; 129 : 189–202. [Google Scholar]
Gow A, Southwood CM, Li JS, et al. CNS myelin and Sertoli cell tight junction strands are absent in Osp/claudin-11 null mice. Cell 1999; 99 : 649–59. [Google Scholar]
Tsukita S, Furuse M. Claudin-based barrier in simple and stratified cellular sheets. Curr Opin Cell Biol 2002; 14 : 531–6. [Google Scholar]
Poliak S, Matlis S, Ullmer C, et al. Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cells. J Cell Biol 2002; 159 : 361–72. [Google Scholar]
Nicholson BJ. Gap junctions : from cell to molecule. J Cell Sci 2003; 116 : 4479–81. [Google Scholar]
Balice-Gordon RJ, Bone LJ, Scherer SS. Functional gap junctions in the schwann cell myelin sheath. J Cell Biol 1998; 142 : 1095–104. [Google Scholar]
Altevogt BM, Kleopa KA, Postma FR, et al. Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems. J Neurosci 2002; 22 : 6458–70. [Google Scholar]
Scherer SS, Deschenes SM, Xu YT, et al. Connexin32 is a myelin-related protein in the PNS and CNS. J Neurosci 1995; 15 : 8281–94. [Google Scholar]
Suter U, Scherer SS. Disease mechanisms in inherited neuropathies. Nat Rev Neurosci 2003; 4 : 714–26. [Google Scholar]
Berger P, Young P, Suter U. Molecular cell biology of Charcot-Marie-Tooth disease. Neurogenetics 2002; 4 : 1–15. [Google Scholar]
Young P, Boussadia O, Berger P, et al. E-cadherin is required for the correct formation of autotypic adherens junctions of the outer mesaxon but not for the integrity of myelinated fibers of peripheral nerves. Mol Cell Neurosci 2002; 21 : 341–51. [Google Scholar]
Yamada H, Denzer AJ, Hori H, et al. Dystroglycan is a dual receptor for agrin and laminin-2 in Schwann cell membrane. J Biol Chem 1996; 271 : 23418–23. [Google Scholar]
Sherman DL, Fabrizi C, Gillespie CS, et al. Specific disruption of a Schwann cell dystrophin-related protein complex in a demyelinating neuropathy. Neuron 2001; 30 : 677–87. [Google Scholar]
Gillespie CS, Sherman DL, Fleetwood-Walker SM, et al. Peripheral demyelination and neuropathic pain behavior in periaxin-deficient mice. Neuron 2000; 26 : 523–31. [Google Scholar]
Boerkoel CF, Takashima H, Stankiewicz P, et al. Periaxin mutations cause recessive Dejerine-Sottas neuropathy. Am J Hum Genet 2001; 68 : 325–33. [Google Scholar]
Guilbot A, Williams A, Ravise N, et al. A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease. Hum Mol Genet 2001; 10 : 415–21. [Google Scholar]
Saito F, Moore SA, Barresi R, et al. Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization. Neuron 2003; 38 : 747–58. [Google Scholar]
Rambukkana A. Mycobacterium leprae-induced demyelination : a model for early degeneration. Curr Opin Immunol 2004; 16 : 511–8. [Google Scholar]
Matsumura K, Yamada H, Saito F, et al. Peripheral nerve involvement in merosin-deficient cognenital muscular dystrophy and dy mouse. Neuromusc. Disorders 1997; 7 :7–12. [Google Scholar]
Salzer JL. Polarized domains of myelinated axons. Neuron 2003; 40 : 297–318. [Google Scholar]
Goutebroze L, Carnaud M, Denisenko N, et al. Syndecan-3 and syndecan-4 are enriched in Schwann cell perinodal processes. BMC Neurosci 2003; 4 : 29. [Google Scholar]
Bhat MA, Rios JC, Lu Y, et al. Axon-glia interactions and the domain organization of myelinated axons require neurexin IV/Caspr/Paranodin. Neuron 2001; 30 : 369–83. [Google Scholar]
Boyle ME, Berglund EO, Murai KK, et al. Contactin orchestrates assembly of the septate-like junctions at the paranode in myelinated peripheral nerve. Neuron 2001; 30 : 385–97. [Google Scholar]
Dupree JL, Girault JA, Popko B. Axo-glial interactions regulate the localization of axonal paranodal proteins. J Cell Biol 1999; 147 : 1145–52. [Google Scholar]
Ishibashi T, Dupree JL, Ikenaka K, et al. A myelin galactolipid, sulfatide, is essential for maintenance of ion channels on myelinated axon but not essential for initial cluster formation. J Neurosci 2002; 22 : 6507–14. [Google Scholar]
Poliak S, Gollan L, Salomon D, et al. Localization of Caspr2 in myelinated nerves depends on axon-glia interactions and the generation of barriers along the axon. J Neurosci 2001; 21 : 7568–75. [Google Scholar]
Poliak S, Salomon D, Elhanany H, et al. Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1. J Cell Biol 2003; 162 : 1149–60. [Google Scholar]
Traka M, Goutebroze L, Denisenko N, et al. Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers. J Cell Biol 2003; 162 : 1161–72. [Google Scholar]

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[1] Arroyo EJ, Scherer SS. On the molecular architecture of myelinated fibers. Histochem Cell Biol 2000; 113 : 1–18. [Google Scholar]

[2] Filbin MT, Tennekoon GI. The role of complex carbohydrates in adhesion of the myelin protein, P0. Neuron 1991; 7 : 845–55. [Google Scholar]

[3] Tetzlaff W. Tight junction contact events and temporary gap junctions in the sciatic nerve fibres of the chicken during Wallerian degeneration and subsequent regeneration. J Neurocytol 1982; 11 : 839–58. [Google Scholar]

[4] Fannon AM, Sherman DL, Ilyina-Gragerova G, et al. Novel E-cadherin-mediated adhesion in peripheral nerve : Schwann cell architecture is stabilized by autotypic adherens junctions. J Cell Biol 1995; 129 : 189–202. [Google Scholar]

[5] Gow A, Southwood CM, Li JS, et al. CNS myelin and Sertoli cell tight junction strands are absent in Osp/claudin-11 null mice. Cell 1999; 99 : 649–59. [Google Scholar]

[6] Tsukita S, Furuse M. Claudin-based barrier in simple and stratified cellular sheets. Curr Opin Cell Biol 2002; 14 : 531–6. [Google Scholar]

[7] Poliak S, Matlis S, Ullmer C, et al. Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cells. J Cell Biol 2002; 159 : 361–72. [Google Scholar]

[8] Nicholson BJ. Gap junctions : from cell to molecule. J Cell Sci 2003; 116 : 4479–81. [Google Scholar]

[9] Balice-Gordon RJ, Bone LJ, Scherer SS. Functional gap junctions in the schwann cell myelin sheath. J Cell Biol 1998; 142 : 1095–104. [Google Scholar]

[10] Altevogt BM, Kleopa KA, Postma FR, et al. Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems. J Neurosci 2002; 22 : 6458–70. [Google Scholar]

[11] Scherer SS, Deschenes SM, Xu YT, et al. Connexin32 is a myelin-related protein in the PNS and CNS. J Neurosci 1995; 15 : 8281–94. [Google Scholar]

[12] Suter U, Scherer SS. Disease mechanisms in inherited neuropathies. Nat Rev Neurosci 2003; 4 : 714–26. [Google Scholar]

[13] Berger P, Young P, Suter U. Molecular cell biology of Charcot-Marie-Tooth disease. Neurogenetics 2002; 4 : 1–15. [Google Scholar]

[14] Young P, Boussadia O, Berger P, et al. E-cadherin is required for the correct formation of autotypic adherens junctions of the outer mesaxon but not for the integrity of myelinated fibers of peripheral nerves. Mol Cell Neurosci 2002; 21 : 341–51. [Google Scholar]

[15] Yamada H, Denzer AJ, Hori H, et al. Dystroglycan is a dual receptor for agrin and laminin-2 in Schwann cell membrane. J Biol Chem 1996; 271 : 23418–23. [Google Scholar]

[16] Sherman DL, Fabrizi C, Gillespie CS, et al. Specific disruption of a Schwann cell dystrophin-related protein complex in a demyelinating neuropathy. Neuron 2001; 30 : 677–87. [Google Scholar]

[17] Gillespie CS, Sherman DL, Fleetwood-Walker SM, et al. Peripheral demyelination and neuropathic pain behavior in periaxin-deficient mice. Neuron 2000; 26 : 523–31. [Google Scholar]

[18] Boerkoel CF, Takashima H, Stankiewicz P, et al. Periaxin mutations cause recessive Dejerine-Sottas neuropathy. Am J Hum Genet 2001; 68 : 325–33. [Google Scholar]

[19] Guilbot A, Williams A, Ravise N, et al. A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease. Hum Mol Genet 2001; 10 : 415–21. [Google Scholar]

[20] Saito F, Moore SA, Barresi R, et al. Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization. Neuron 2003; 38 : 747–58. [Google Scholar]

[21] Rambukkana A. Mycobacterium leprae-induced demyelination : a model for early degeneration. Curr Opin Immunol 2004; 16 : 511–8. [Google Scholar]

[22] Matsumura K, Yamada H, Saito F, et al. Peripheral nerve involvement in merosin-deficient cognenital muscular dystrophy and dy mouse. Neuromusc. Disorders 1997; 7 :7–12. [Google Scholar]

[23] Salzer JL. Polarized domains of myelinated axons. Neuron 2003; 40 : 297–318. [Google Scholar]

[24] Goutebroze L, Carnaud M, Denisenko N, et al. Syndecan-3 and syndecan-4 are enriched in Schwann cell perinodal processes. BMC Neurosci 2003; 4 : 29. [Google Scholar]

[25] Bhat MA, Rios JC, Lu Y, et al. Axon-glia interactions and the domain organization of myelinated axons require neurexin IV/Caspr/Paranodin. Neuron 2001; 30 : 369–83. [Google Scholar]

[26] Boyle ME, Berglund EO, Murai KK, et al. Contactin orchestrates assembly of the septate-like junctions at the paranode in myelinated peripheral nerve. Neuron 2001; 30 : 385–97. [Google Scholar]

[27] Dupree JL, Girault JA, Popko B. Axo-glial interactions regulate the localization of axonal paranodal proteins. J Cell Biol 1999; 147 : 1145–52. [Google Scholar]

[28] Ishibashi T, Dupree JL, Ikenaka K, et al. A myelin galactolipid, sulfatide, is essential for maintenance of ion channels on myelinated axon but not essential for initial cluster formation. J Neurosci 2002; 22 : 6507–14. [Google Scholar]

[29] Poliak S, Gollan L, Salomon D, et al. Localization of Caspr2 in myelinated nerves depends on axon-glia interactions and the generation of barriers along the axon. J Neurosci 2001; 21 : 7568–75. [Google Scholar]

[30] Poliak S, Salomon D, Elhanany H, et al. Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1. J Cell Biol 2003; 162 : 1149–60. [Google Scholar]

[31] Traka M, Goutebroze L, Denisenko N, et al. Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers. J Cell Biol 2003; 162 : 1161–72. [Google Scholar]