WNT-7a induces axonal remodeling and increases synapsin I levels in cerebellar neurons

Developmental Biology

Volumn 192, Issue 1, 1997, Pages 31-44

  Lucas, Fiona R ^a   Salinas, Patricia C ^a  

^a KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BETA CATENIN; LITHIUM; RNA; SYNAPSIN I;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CEREBELLUM; CONTROLLED STUDY; CYTOSKELETON; EMBRYO; GENE; GRANULE CELL; IMMUNOBLOTTING; IN SITU HYBRIDIZATION; MOUSE; NERVE FIBER; NONHUMAN; NORTHERN BLOTTING; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL;

EID: 0031469645     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1006/dbio.1997.8734     Document Type: Article

References (60)

1. Alder J., Cho N. K., Hatten M. E. Embryonic precursor cells from the rhombic lip are specified to a cerebellar granule neuron identity. Neuron. 17:1996;389-399.
2. Altman J. Postnatal development of the cerebellar cortex in the rat. 3. Maturation of the components of the granular layer. J. Comp. Neurol. 145:1972a;465-513.
3. Altman J. Postnatal development of the cerebellar cortex in the rat. II. Phases in the maturation of Purkinje cells and the molecular layer. J. Comp. Neurol. 145:1972b;399-464.
4. Atack J. R., Broughton H. B., Pollack S. J. Inositol monophosphatase - A putative target for Li+ in the treatment of bipolar disorder. Trends Neurosci. 18:1995;343-349.
5. Baird D. H., Hatten M. E., Heintz N., Mason C. A. Micromethods for analyzing axon-target interactions in vitro. Neuroprotocols. 4:1994;106-115.
6. Baird D. H., Hatten M. E., Mason C. A. Cerebellar target neurons provide a stop signal for afferent neurite extension in vitro. J. Neurosci. 12:1992;619-634.
7. Baptista C. A., Hatten M. E., Blazeski R., Mason C. A. Cell-cell interactions influence survival and differentiation of purified Purkinje cells in vitro. Neuron. 12:1994;243-260.
8. Berridge M. J., Downes C. P., Hanley M. R. Neural and developmental actions of lithium: A unifying hypothesis. Cell. 59:1989;411-419.
9. Chin L. S., Li L., Ferreira A., Kosik K. S., Greengard P. Impairment of axonal development and of synaptogenesis in hippocampal neurons of synapsin I-deficient mice. Proc. Natl. Acad. Sci. USA. 92:1995;9230-9234.
10. Chomczynski P., Sacchi N. Acid-guanidinium-phenol-chloroform RNA extraction protocol. Anal. Biochem. 162:1987;156-159.
11. Cook D., Fry M. J., Hughes K., Sumathipala R., Woodgett J. R., Dale T. C. Wingless inactivates glycogen synthase kinase-3 via an intracellular signalling pathway which involves a protein kinase C. EMBO J. 15:1996;4526-4536.
12. Fletcher T. L., De Camilli P., Banker G. Synaptogenesis in hippocampal cultures: Evidence indicating that axons and dendrites become competent to form synapses at different stages of neuronal development. J. Neurosci. 14:1994;6695-6706.
13. Fradkin L. G., Noordermeer J. N., Nusse R. The Drosophila Wnt protein DWnt-3 is a secreted glycoprotein localized on the axon tracts of the embryonic CNS. Dev. Biol. 168:1995;202-213.
14. Frantz G. D., Weimann J. M., Levin M. E., McConnell S. K. Otx1 and Otx2 define layers and regions in developing cerebral cortex and cerebellum. J. Neurosci. 14:1994;5725-5740.
15. Gao W. Q., Hatten M. E. Neuronal differentiation rescued by implantation of weaver granule cell precursors into wild-type cerebellar cortex. Science. 260:1993;367-369.
16. Gao W. Q., Liu X. L., Hatten M. E. The weaver gene encodes a nonautonomous signal for CNS neuronal differentiation. Cell. 68:1992;841-854.
17. Goodman C. S. Mechanisms and molecules that control growth cone guidance. Annu. Rev. Neurosci. 19:1996;341-377.
18. Goslin K., Schreyer D. J., Skene J. H. P., Banker G. Changes in the distribution of GAP-43 during the development of neuronal polarity. J. Neurosci. 10:1990;588-602.
19. Guidato S., Tsai L. H., Woodgett J., Miller C. C. J. Differential cellular phosphorylation of neurofilament heavy side-arms by glycogen synthase kinase-3 and cyclin-dependent kinase-5. J. Neurochem. 66:1996;1698-1706.
20. Hamori J., Somogyi J. Differentiation of cerebellar mossy fiber synapses in the rat: A quantitative electron microscope study. J. Comp. Neurol. 220:1983;365-377.
21. Hatten M. E. Neuronal regulation of astroglial morphology and proliferation in vitro. J. Cell Biol. 100:1985;384-396.
22. Hatten M. E., Heintz N. Mechanisms of neural pattering and specification in the developing cerebellum. Annu. Rev. Neurosci. 18:1995;385-408.
23. He X., Saint Jeanneti J. P., Woodgett J. R., Varmus H. E., Dawld I. B. Glycogen synthase kinase-3 and dorsoventral patterning in Xenopus embryos. Nature. 374:1995;617-622.
24. Hedgepeth C. M., Conrad L. J., Zhang J., Huang H-C., Lee V. M. Y., Klein P. S. Activation of the Wnt signaling pathway: A molecular mechanism for lithium action. Dev. Biol. 185:1997;82-91.
25. Herman M. A., Vassilieva L. L., Horvitz H. R., Shaw J. E., Herman R. K. TheC. elegans. Cell. 83:1995;101-110.
26. Hooper J. E. Distinct pathways for autocrine and paracrine wingless signalling in Drosophila embryos. Nature. 372:1994;461-464.
27. Ingham P. W., Martinez A. A. Boundaries and fields in early embryos. Cell. 68:1992;221-235.
28. Ito M. The Cerebellum and Neural Control. 1984;Raven Press, New York.
29. Jaarsma D., Dino M. R., Cozzari C., Mugnaini E. Cerebellar choline acetyltransferase positive mossy fibres and their granule and unipolar brush cell targets: A model for central cholinergic nicotinic neurotransmission. J. Neurocytol. 25:1996;829-842.
30. Joyner A. L. Engrailed, Wnt and Pax genes regulate midbrain-hindbrain development. Trends Genet. 12:1996;15-20.
31. Kennedy T. E., Tessier Lavigne M. Guidance and induction of branch formation in developing axons by target-derived diffusible factors. Curr. Opin. Neurobiol. 5:1995;83-90.
32. Keynes R., Cook G. M. W. Axon guidance molecules. Cell. 83:1995;161-169.
33. Klein P. S., Melton D. A. A molecular mechanism for the effect of lithium on development. Proc. Natl. Acad. Sci. USA. 93:1996;8455-8459.
34. Kleitman N., Wood P. M., Bunge R. P. Tissue culture methods for the study of myelination. Culturing Nerve Cells. 1991;MIT Press, Cambridge. p. 351-353.
35. Mandelkow E. M., Biernat J., Drewes G., Gustke N., Trinczek B., Mandelkow E. Tau domains, phosphorylation, and interactions with microtubules. Neurobiol. Aging. 16:1995;355-362.
36. Millen K. J., Hui C. C., Joyner A. L. A role for En-2 and other murine homologues of Drosophila segment polarity genes in regulating positional information in the developing cerebellum. Development. 121:1995;3935-3945.
37. Miller J. R., Moon R. T. Signal transduction through beta-catenin and specification of cell fate during embryogenesis. Genes Dev. 10:1996;2527-2539.
38. Moon R. T., Brown J. D., Yang Snyder J. A., Miller J. R. Structurally related receptors and antagonists compete for secreted Wnt ligands. Cell. 88:1997;725-728.
39. Munemitsu S., Souza B., Muller O., Albert I., Rubinfeld B., Polakis P. The APC gene product associates with microtubules in vivo and promotes their assembly in vitro. Cancer Res. 54:1994;3676-3681.
40. Nusse R. A versatile transcription effect of Wingless signaling. Cell. 89:1997;321-323.
41. Nusse R., Varmus H. E. WNT. Cell. 69:1992;1073-1087.
42. Papkoff J. Regulation of complexed and free catenin pools by distinct mechanisms. Differential effects of Wnt-1 and v-Src. J. Biol. Chem. 272:1997;4536-4543.
43. Parr B. A., McMahon A. P. Wnt genes and vertebrate development. Curr. Opin. Genet. Dev. 4:1994;523-528.
44. Parr B. A., McMahon A. P. Dorsalizing signal Wnt-7a required for normal polarity of D-V and A-P axes of mouse limb. Nature. 374:1995;350-353.
45. Peifer M., Sweeton D., Casey M., Wieschaus E. wingless signal and Zeste-white 3 kinase trigger opposing changes in the intracellular distribution of Armadillo. Development. 120:1994;369-380.
46. Ramakrishna N. R., Brown A. Wingless, the Drosophila homolog of the proto-oncogene Wnt-1, can transform mouse mammary epithelial cells. Development. 119:1993;95-103.
47. Roelink H. Tripartite signaling of pattern: Interactions between Hedgehogs, BMPs and Wnts in the control of vertebrate development. Curr. Opin. Neurobiol. 6:1996;33-40.
48. Rosahl T. W., Spillane D., Missler M., Herz J., Selig D. K., Wolff J. R., Hammer R. E., Malenka R. C., Sudhof T. C. Essential functions of synapsins I and II in synaptic vesicle regulation. Nature. 375:1995;488-493.
49. Salinas P. C., Fletcher C., Copeland N. G., Jenkins N. A., Nusse R. Maintenance of Wnt-3 expression in Purkinje cells of the mouse cerebellum depends on interactions with granule cells. Development. 120:1994;1277-1286.
50. Smith K. J., Levy D. B., Maupin P., Pollard T. D., Vogelstein B., Kinzler K. W. Wild-type but not mutant APC associates with the microtubule cytoskeleton. Cancer Res. 54:1994;3672-3675.
51. Snyder E. Y., Deitcher D. L., Walsh C., Arnold A. S., Hartwieg E. A., Cepko C. L. Multipotent neural cell lines can engraft and participate in development of mouse cerebellum. Cell. 68:1992;33-51.
52. Sotelo C. Cerebellar synaptogenesis: What we can learn from mutant mice. J. Exp. Biol. 153:1990;225-249.
53. Stambolic V., Ruel L., Woodgett J. R. Lithium inhibits glycogen synthase kinase-3 activity and mimics Wingless signalling in intact cells. Curr. Biol. 6:1996;1664-1668.
54. Stoykova A., Gruss P. Roles of Pax-genes in developing and adult brain as suggested by expression patterns. J. Neurosci. 14:1994;1395-1412.
55. Su L. K., Vogelstein B., Kinzler K. W. Association of the APC tumor suppressor protein with catenins. Science. 262:1993;1734-1737.
56. Takahashi M., Tomizawa K., Kato R., Sato K., Uchida T., Fujita S. C., Imahori K. Localization and developmental changes of tau protein kinase I/glycogen synthase kinase-3beta in rat brain. J. Neurochem. 63:1994;245-255.
57. Tao Y. S., Edwards R. A., Tubb B., Wang S., Bryan J., McCrea P. D. beta-Catenin associates with the actin-bundling protein fascin in a noncadherin complex. J. Cell Biol. 134:1996;1271-1281.
58. Tessier Lavigne M., Goodman C. S. The molecular biology of axon guidance. Science. 274:1996;1123-1133.
59. Wagner U., Utton M., Gallo J. M., Miller C. C. J. Cellular phosphorylation of tau by GSK-3beta influences tau binding to microtubules and microtubule organisation. J. Cell Sci. 109:1996;1537-1543.
60. Yost C., Torres M., Miller J. R., Huang E., Kimelman D., Moon R. T. The axis-inducing activity, stability, and subcellular distribution of beta-catenin is regulated in Xenopus embryos by glycogen synthase kinase 3. Genes Dev. 10:1996;1443-1454.