Accumulation of NaV1 mRNAs at differentiating postsynaptic sites in rat soleus muscles

Molecular and Cellular Neuroscience

Volumn 28, Issue 4, 2005, Pages 694-702

  Stocksley, Mark A ^a,c   Awad, Suad S ^a   Young, Carol ^a   Lightowlers, Robert N ^a   Brenner, Hans Rudolf ^b   Slater, Clarke R ^a  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

^b UNIVERSITY OF BASEL   (Switzerland)

^c UNIVERSITY OF OTTAWA HEART INSTITUTE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AGRIN; CHOLINERGIC RECEPTOR; ISOPROTEIN; MESSENGER RNA; UNCLASSIFIED DRUG; VOLTAGE GATED CALCIUM CHANNEL ALPHA SUBUNIT 1.4 PROTEIN; VOLTAGE GATED CALCIUM CHANNEL ALPHA SUBUNIT 1.5 PROTEIN; VOLTAGE GATED CHANNEL FORMING PROTEIN; NERVE PROTEIN; SODIUM CHANNEL;

ANIMAL TISSUE; ARTICLE; BINDING SITE; BIRTH; CONTROLLED STUDY; DENERVATION; EMBRYO; GENE CLUSTER; GENE CONTROL; GENETIC CODE; IN SITU HYBRIDIZATION; MOUSE; MUSCLE REGENERATION; NEUROMUSCULAR SYNAPSE; NEWBORN; NONHUMAN; POSTSYNAPTIC MEMBRANE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN FOLDING; RAT; SOLEUS MUSCLE; UPREGULATION; ANIMAL; BIOSYNTHESIS; COMPARATIVE STUDY; GROWTH, DEVELOPMENT AND AGING; METABOLISM; PRENATAL DEVELOPMENT; SKELETAL MUSCLE; SYNAPSE;

MURINAE;

ANIMALS; ANIMALS, NEWBORN; MUSCLE, SKELETAL; NERVE TISSUE PROTEINS; NEUROMUSCULAR JUNCTION; RATS; RNA, MESSENGER; SODIUM CHANNELS; SYNAPSES;

EID: 15244359235     PISSN: 10447431     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mcn.2004.11.015     Document Type: Article

References (48)

1. S.S. Awad, R.N. Lightowlers, C. Young, Z.M. Chrzanowska-Lightowlers, T. Lomo, and C.R. Slater Sodium channel mRNAs at the neuromuscular junction: distinct patterns of accumulation and effects of muscle activity J. Neurosci. 21 2001 8456 8463
2. S.S. Awad, M.A. Stocksley, A. Buckel, R.N. Lightowlers, and C.R. Slater Rapid accumulation of NaV1 mRNAs at newborn rat neuromuscular junctions 2002 Abstract Viewer/Itinerary Planner Society for Neuroscience Program No. 699.2 2002
3. C.R. Bader, D. Bertrand, E. Cooper, and A. Mauro Membrane currents of rat satellite cells attached to intact skeletal muscle fibers Neuron 1 1988 237 240
4. V1 channels and ankyrinG occupy a different postsynaptic domain from AChRs from an early stage of neuromuscular junction formation in rats J. Neurosci. 23 2003 2102 2111
5. G.B. Banks, C. Fuhrer, M.E. Adams, and S.C. Froehner The postsynaptic submembrane machinery at the neuromuscular junction: requirement for rapsyn and the utrophin/dystrophin-associated complex J. Neurocytol. 32 2003 709 726
6. H.R. Brenner, V. Witzemann, and B. Sakmann Imprinting of acetylcholine receptor messenger RNA accumulation in mammalian neuromuscular synapses Nature 344 1990 544 547
7. H.R. Brenner, A. Herczeg, and C.R. Slater Synapse-specific expression of acetylcholine receptor genes and their products at original synaptic sites in rat soleus muscle fibres regenerating in the absence of innervation Development 116 1992 41 53
8. H.R. Brenner, S. Rotzler, W.A. Kues, V. Witzemann, and B. Sakmann Nerve-dependent induction of AChR epsilon-subunit gene expression in muscle is independent of state of differentiation Dev. Biol. 165 1994 527 536
9. M.E. Burns, and G.J. Augustine Synaptic structure and function: dynamic organization yields architectural precision Cell 83 1995 187 194
10. W.A. Catterall Cellular and molecular biology of voltage-gated sodium channels Physiol. Rev. 72 1992 S15 S48
11. J.V. Chakkalakal, and B.J. Jasmin Localizing synaptic mRNAs at the neuromuscular junction: it takes more than transcription Bioessays 25 2003 25 31
12. I. Cohen, M. Rimer, T. Lomo, and U.J. McMahan Agrin-induced postsynaptic-like apparatus in skeletal muscle fibers in vivo Mol. Cell. Neurosci. 9 1997 237 253
13. G. Corfas, and G.D. Fischbach The number of Na+ channels in cultured chick muscle is increased by ARIA, an acetylcholine receptor-inducing activity J. Neurosci. 13 1993 2118 2125
14. D.E. de Kerchove, J. Cartaud, A. Ravel-Chapuis, T. Seroz, F. Pasteau, L.M. Angus, B.J. Jasmin, J.P. Changeux, and L. Schaeffer Expression of mutant Ets protein at the neuromuscular synapse causes alterations in morphology and gene expression EMBO Rep. 3 2002 1075 1081
15. H.C. Fertuck, and M.M. Salpeter Localization of acetylcholine receptor by 125I-labeled alpha-bungarotoxin binding at mouse motor endplates Proc. Natl. Acad. Sci. U. S. A. 71 1974 1376 1378
16. B.E. Flucher, and M.P. Daniels Distribution of Na+ channels and ankyrin in neuromuscular junctions is complementary to that of acetylcholine receptors and the 43 kd protein Neuron 3 1989 163 175
17. L. Fromm, and M. Rhode Neuregulin-1 induces expression of Egr-1 and activates acetylcholine receptor transcription through an Egr-1-binding site J. Mol. Biol. 339 2004 483 494
18. D. Goldman, B.M. Carlson, and J. Staple Induction of adult-type nicotinic acetylcholine receptor gene expression in noninnervated regenerating muscle Neuron 7 1991 649 658
19. B. Haimovich, E. Bonilla, J. Casadei, and R. Barchi Immunocytochemical localization of the mammalian voltage-dependent sodium channel using polyclonal antibodies against the purified protein J. Neurosci. 4 1984 2259 2268
20. J.B. Harris, and M.A. Johnson Further observations on the pathological responses of rat skeletal muscle to toxins isolated from the venom of the Australian tiger snake, Notechis scutatus scutatus Clin. Exp. Pharmacol. Physiol. 5 1978 587 600
21. S. Hashemolhosseini, C. Moore, L. Landmann, A. Sander, H. Schwarz, V. Witzemann, B. Sakmann, and H.R. Brenner Electrical activity and postsynapse formation in adult muscle: gamma-AChRs are not required Mol. Cell. Neurosci. 16 2000 697 707
22. S.A. Jo, and S.J. Burden Synaptic basal lamina contains a signal for synapse-specific transcription Development 115 1992 673 680
23. G. Jones, T. Meier, M. Lichtsteiner, V. Witzemann, B. Sakmann, and H.R. Brenner Induction by agrin of ectopic and functional postsynaptic-like membrane in innervated muscle Proc. Natl. Acad. Sci. U. S. A. 94 1997 2654 2659
24. G. Jones, C. Moore, S. Hashemolhosseini, and H.R. Brenner Constitutively active MuSK is clustered in the absence of agrin and induces ectopic postsynaptic-like membranes in skeletal muscle fibers J. Neurosci. 19 1999 3376 3383
25. W.A. Kues, H.R. Brenner, B. Sakmann, and V. Witzemann Local neurotrophic repression of gene transcripts encoding fetal AChRs at rat neuromuscular synapses J. Cell Biol. 130 1995 949 957
26. W.A. Kues, B. Sakmann, and V. Witzemann Differential expression patterns of five acetylcholine receptor subunit genes in rat muscle during development Eur. J. Neurosci. 7 1995 1376 1385
27. E. Lacazette, S. Le Calvez, N. Gajendran, and H.R. Brenner A novel pathway for MuSK to induce key genes in neuromuscular synapse formation J. Cell Biol. 161 2003 727 736
28. Q. Li, R.M. Esper, and J.A. Loeb Synergistic effects of neuregulin and agrin on muscle acetylcholine receptor expression Mol. Cell. Neurosci. 26 2004 558 569
29. T. Lomo, and C.R. Slater Control of junctional acetylcholinesterase by neural and muscular influences in the rat J. Physiol. 303 1980 191 202
30. M.T. Lupa, and J.H. Caldwell Sodium channels aggregate at former synaptic sites in innervated and denervated regenerating muscles J. Cell Biol. 124 1994 139 147
31. M.T. Lupa, D.M. Krzemien, K.L. Schaller, and J.H. Caldwell Aggregation of sodium channels during development and maturation of the neuromuscular junction J. Neurosci. 13 1993 1326 1336
32. A.R. Martin Amplification of neuromuscular transmission by postjunctional folds Proc. R. Soc. Lond., B Biol. Sci. 258 1994 179 187
33. U.J. McMahan The agrin hypothesis Cold Spring Harbor Symp. Quant. Biol. 55 1990 407 418
34. U.J. McMahan, and C.R. Slater The influence of basal lamina on the accumulation of acetylcholine receptors at synaptic sites in regenerating muscle J. Cell Biol. 98 1984 1453 1473
35. T. Meier, D.M. Hauser, M. Chiquet, L. Landmann, M.A. Ruegg, and H.R. Brenner Neural agrin induces ectopic postsynaptic specializations in innervated muscle fibers J. Neurosci. 17 1997 6534 6544
36. A. Sander, A. Guth, H.R. Brenner, and V. Witzemann Gene transfer into individual muscle fibers and conditional gene expression in living animals Cell Tissue Res. 301 2000 397 403
37. A.W. Sandrock Jr., S.E. Dryer, K.M. Rosen, S.N. Gozani, R. Kramer, L.E. Theill, and G.D. Fischbach Maintenance of acetylcholine receptor number by neuregulins at the neuromuscular junction in vivo Science 276 1997 599 603
38. J.R. Sanes, and J.W. Lichtman Development of the vertebrate neuromuscular junction Annu. Rev. Neurosci. 22 1999 389 442
39. J.R. Sanes, and J.W. Lichtman Induction, assembly, maturation and maintenance of a postsynaptic apparatus Nat. Rev., Neurosci. 2 2001 791 805
40. A.A. Sharp, and J.H. Caldwell Aggregation of sodium channels induced by a postnatally upregulated isoform of agrin J. Neurosci. 16 1996 6775 6783
41. R. Vater, C. Young, L.V.B. Anderson, S. Lindsay, D.J. Blake, K.E. Davies, R. Zuellig, and C.R. Slater Utrophin mRNA expression in muscle is not restricted to the neuromuscular junction Mol. Cell. Neurosci. 10 1998 229 242
42. R.E. Weiss, and R. Horn Functional differences between two classes of sodium channels in developing rat skeletal muscle Science 233 1986 362 364
43. V. Witzemann, B. Barg, M. Criado, E. Stein, and B. Sakmann Developmental regulation of five subunit specific mRNAs encoding acetylcholine receptor subtypes in rat muscle FEBS Lett. 242 1989 419 424
44. S.J. Wood, and C.R. Slater beta-Spectrin is colocalized with both voltage-gated sodium channels and ankyrinG at the adult rat neuromuscular junction J. Cell Biol. 140 1998 675 684
45. S.J. Wood, and C.R. Slater Safety factor at the neuromuscular junction Prog. Neurobiol. 64 2001 393 429
46. S.J. Wood, K. Shewry, C. Young, and C.R. Slater An early stage in sodium channel clustering at developing rat neuromuscular junctions NeuroReport 9 1998 1991 1995
47. C. Young, S. Lindsay, R. Vater, and C.R. Slater An improved method for the simultaneous demonstration of mRNA and esterase activity at the human neuromuscular junction Histochem. J. 30 1998 7 11
48. M. Zhang, and I.S. McLennan During secondary myotube formation, primary myotubes preferentially absorb new nuclei at their ends Dev. Dyn. 204 1995 168 177