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Original Article

GAP-43 mRNA Expression in Facial Motoneurons During Regeneration: In situ Hybridization Histochemistry Study Using an Alkaline Phosphatase-labelled Probe

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Pages 80-84 | Published online: 08 Jul 2009

References

  • Liu Y, Storm D R. Regulation of free calmodulin levels by neuromodulin: neuron growth and regeneration. Trends Pharmacol Sci 1990; 11: 107–11
  • Skene J H P. Axonal growth‐associated proteins. Ann Rev Neurosci 1989; 12: 127–56
  • Basi G S., Jacobson R D., Virag I, Schilling J, Skene J H P. Primary structure and transcriptional regulation of GAP‐43, a protein associated with nerve growth. Cell 1987; 49: 785–91
  • Karns L R., Ng S ‐H, Freeman J A., Fishman M C. Cloning of complementary DNA for GAP‐43, a neuronal growth‐related protein. Science 1987; 236: 597–600
  • Neve R L., Perrone‐Bizzozero N I., Finklestein S, Zwiers H, Bird E, Kurnit D M., Benowitz L I. The neuronal growth associated protein GAP‐43 (B‐50, Fl): neuronal specificity, developmental regulation and regional distribution of the human and rat mRNAs. Mol Brain Res 1987; 2: 177–83
  • Hoffman P N. Expression of GAP‐43, a rapidly transported growth‐associated protein, and class II beta tubulin, a slowly transported cytoskeletal protein, are coordinated in regenerating neurons. J Neurosci 1989; 9: 893–7
  • Van der Zee C EEM, Nielander H B., Vos J P., Lopes da Silva S, Verhaagen J, Oestreicher A B., Schrama L H., Schotman P, Gispen W H. Expression of growth associated protein B‐50 (GAP‐43) in dorsal root ganglia and sciatic nerve during regenerative sprouting. J Neurosci 1989; 9: 3505–12
  • Verge V M K, Tetzlaff W, Richardson P M., Bisby M A. Correlation between GAP‐43 and nerve growth factor receptors in rat sensory neurons. J Neurosci 1990; 10: 926–34
  • Bisby M A. Dependence of GAP 43 (B50, Fl) transport on axonal regeneration in rat dorsal root ganglion neurons. Brain Res 1988; 458: 157–61
  • Tetzlaff W, Zwiers H, Lederis K, Cassar L, Bisby M A. Axonal transport and localization of B‐50/GAP‐43‐like immunoreactivity in regenerating sciatic and facial nerves of the rat. J Neurosci 1989; 9: 1303–13
  • Tetzlaff W, Alexander S W., Miller F D., Bisby M A. Response of facial and rubrospinal neurons to axotomy: changes in mRNA expression for cytoskeletal proteins and GAP‐43. J Neurosci 1991; 11: 2528–44
  • Verge V M K, Riopelle R J., Richardson P M. Nerve growth factor receptors on normal and injured sensory neurons. J Neurosci 1989; 9: 914–22
  • Ernfors P, Henschen A, Olson L, Persson H. Expression of nerve growth factor receptor mRNA is developmentally regulated and increased after axotomy in rat spinal cord motoneurons. Neuron 1989; 2: 1605–13
  • Saika T, Senba E, Noguchi K, Sato M, Yoshida S, Kubo T, Matsunaga T, Tohyama M. Effects of nerve crush and transection on mRNA levels for nerve growth factor receptor in the rat facial motoneurons. Mol Brain Res 1991; 9: 157–60
  • Wood S J., Pritchard J, Sofroniew M V. Re‐expression of nerve growth factor receptor after axonal injury recapitulates a developmental event in motor neurons: differential regulation when regeneration is allowed or prevented. Eur J Neurosci 1990; 2: 650–7
  • Noguchi K, Senba E, Morita Y, Sato M, Tohyama M. α‐CGRP and β‐CGRP mRNAs are differentially regulated in the rat spinal cord and dorsal root ganglion. Mol Brain Res 1990; 7: 299–304
  • Kiyama H, Emson P C. Distribution of somatostatin mRNA in the rat nervous system as visualized by a novel non‐radioactive in situ hybridization histochemistry procedure. Neuroscience 1990; 38: 223–44
  • Kiyama H, Emson P C., Tohyama M. Recent progress in the use of the technique of non‐radioactive in situ hybridization histochemistry: new tools for molecular neurobiology. Neurosci Res 1990; 9: 1–21
  • Kiyama H, Emson P C., Ruth J, Morgan C. Sensitive non‐radioisotopic in situ hybridization histochemistry: demonstration of tyrosine hydroxylase gene expression in rat brain and adrenal. Mol Brain Res 1990; 7: 213–9
  • Federoff H J., Grabczyk Ed, Fishman M C. Dual regulation of GAP‐43 gene expression by nerve growth factor and glucocorticoids. J Biol Chem 1988; 263: 19290–5
  • Van Hooff C O M, De Graan P N E, Boonstra J, Oestreicher A B., Schmidt‐Michels M H., Gispen W H. Nerve growth factor enhances the level of the protein kinase C substrate B‐50 in pheochromocytoma PC12 cells. Biochem Biophys Res Commun 1986; 139: 644–51
  • Van Hooff C O M, Holthuis J C M, Oestreicher A B., Boonstra J, De Graan P N E, Gispen W H. Nerve growth factor‐induced changes in the intracellular localization of the protein kinase C substrate B‐50 in pheochromocytoma PC12 cells. J Cell Biol 1989; 108: 1115–25
  • Meiri K F., Burdick D. Nerve growth factor stimulation of GAP‐43 phosphorylation in intact isolated growth cones. J Neurosci 1991; 11: 3155–64
  • Kaplan D R., Hempstead B L., Martin‐Zanca D, Chao M V., Parada L F. The trk proto‐oncogene product: signal transducing receptor for nerve growth factor. Science 1991; 252: 554–8
  • Nebreda A R., Martin‐Zanka D, Kaplan D R., Parada L F., Santos E. Induction by NGF of meiotic maturation of xenopus oocytes expressing the trk proto‐oncogene product. Science 1991; 252: 558–61

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