Transient expression of GABAA receptor α2 and α3 subunits in differentiating cerebellar neurons

Developmental Brain Research

Volumn 148, Issue 2, 2004, Pages 169-177

  Takayama, Chitoshi ^a   Inoue, Yoshiro ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

Author keywords

Bergmann glia; Cerebellar nucleus; Granule cell; In situ hybridization; Purkinje cell

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR; 4 AMINOBUTYRIC ACID A RECEPTOR ALPHA2; 4 AMINOBUTYRIC ACID A RECEPTOR ALPHA3; MESSENGER RNA; RECEPTOR SUBUNIT; UNCLASSIFIED DRUG; PROTEIN SUBUNIT;

ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; BRAIN NERVE CELL; CELL MATURATION; CEREBELLUM; CEREBELLUM NUCLEUS; EMBRYO DEVELOPMENT; IN SITU HYBRIDIZATION; MOUSE; NERVE CELL DIFFERENTIATION; NEWBORN; NONHUMAN; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; PURKINJE CELL; STEM CELL; ANIMAL; C57BL MOUSE; CELL COUNT; CELL DIFFERENTIATION; COMPARATIVE STUDY; CYTOLOGY; EMBRYO; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; METHODOLOGY; NERVE CELL; PHYSIOLOGY; PRENATAL DEVELOPMENT;

MAMMALIA;

ANIMALS; CELL COUNT; CELL DIFFERENTIATION; CEREBELLUM; EMBRYO; GENE EXPRESSION REGULATION, DEVELOPMENTAL; IN SITU HYBRIDIZATION; MICE; MICE, INBRED C57BL; NEURONS; PROTEIN SUBUNITS; RECEPTORS, GABA-A;

EID: 0842346200     PISSN: 01653806     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.devbrainres.2003.11.007     Document Type: Article

References (63)

1. Abraham J.H., Schousboe A. Effects of taurine on cell morphology and expression of low-affinity GABA receptors in cultured cerebellar granule cells. Neurochem. Res. 14:1989;1031-1038.
2. Altman J., Bayer S.A. Development of the cerebellar system in relation to its evolution, structure, and functions. 1997;CPC Press, Boca Raton. 783 pp.
3. Araki T., Kiyama H., Tohyama M. GABAA receptor subunit messenger RNAs show differential expression during cortical development in the rat brain. Neuroscience. 51:1992;583-591.
4. Barbin G., Pollard H., Gaiarsa J.L., Ben-Ari Y. Involvement of GABAA receptors in the outgrowth of cultured hippocampal neurons. Neurosci. Lett. 152:1993;150-154.
5. Barker J.L., Behar T., Li Y.X., Liu Q.Y., Ma W., Maric D., Maric I., Schaffner A.E., Serafini R., Smith S.V., Somogyi R., Vautrin J.Y., Wen X.L., Xian H. GABAergic cells and signals in CNS development. Perspect. Dev. Neurobiol. 5:1998;305-322.
6. Barker J.L., Behar T.N., Ma W., Maric D., Maric I. GABA emerges as a developmental signal during neurogenesis of the rat central nervous system. Martin D.L., Olsen R.W. GABA in the Nervous System: the View at Fifty Years. 2000;245-263 Lippincott Williams and Wilkins, Philadelphia.
7. Belhage B., Hansen G.H., Elster L., Schousboe A. Effects of gamma-aminobutyric acid (GABA) on synaptogenesis and synaptic function. Perspect. Dev. Neurobiol. 5:1998;235-246.
8. Ben-Ari Y. Excitatory actions of gaba during development: the nature of the nurture. Nat. Rev. Neurosci. 3:2002;728-739.
9. Carlson B.X., Elster L., Schousboe A. Pharmacological and functional implications of developmentally-regulated changes in GABA(A) receptor subunit expression in the cerebellum. Eur. J. Pharmacol. 352:1998;1-14.
10. Cherubini E., Gaiarsa J.L., Ben-Ari Y. GABA: an excitatory transmitter in early postnatal life. Trends Neurosci. 14:1991;515-519.
11. Fairen A., Alvarez-Bolado G., DeDiego I., Smith-Fernandez A. GABA-immunoreactive cells of the cortical primordium contribute to distinctly fated neuronal populations. Perspect. Dev. Neurobiol. 5:1998;159-173.
12. Fritschy J.M., Paysan J., Enna A., Mohler H. Switch in the expression of rat GABAA-receptor subtypes during postnatal development: an immunohistochemical study. J. Neurosci. 14:1994;5302-5324.
13. Frostholm A., Zdilar D., Chang A., Rotter A. Stability of GABAA/benzodiazepine receptor alpha 1 subunit mRNA expression in reeler mouse cerebellar Purkinje cells during postnatal development. Brain Res. Dev. Brain Res. 64:1991;121-128.
14. Gambarana C., Pittman R., Siegel R.E. Developmental expression of the GABAA receptor alpha 1 subunit mRNA in the rat brain. J. Neurobiol. 21:1990;1169-1179.
15. Gao B., Fritschy J.M. Cerebellar granule cells in vitro recapitulate the in vivo pattern of GABAA-receptor subunit expression. Brain Res. Dev. Brain Res. 88:1995;1-16.
16. Gao X.B., van den Pol A.N. GABA release from mouse axonal growth cones. J. Physiol. 523(Pt 3):2000;629-637.
17. Haydar T.F., Wang F., Schwartz M.L., Rakic P. Differential modulation of proliferation in the neocortical ventricular and subventricular zones. J. Neurosci. 20:2000;5764-5774.
18. Ito M. The Cerebellum and Neural Control. 1984;Raven Press, New York.
19. Jacobson M. Developmental Neurobiology. 1991;Plenum, New York.
20. Kardos J. Recent advances in GABA research. Neurochem. Int. 34:1999;353-358.
21. Komuro H., Yacubova E. Migration of cerebellar granule cell. Cell Technol. 20:2001;513-519.
22. Komuro H., Yacubova E., Rakic P. Mode and tempo of tangential cell migration in the cerebellar external granular layer. J. Neurosci. 21:2001;527-540.
23. Larramendi L.H.M. Analysis of synaptogenesis in the cerebellum of the mouse. Llinas R. Neurobiology of Cerebellar Evolution and Development. 1969;783-843 Am. Med. Assoc. Chicago.
24. Lauder J.M. Neurotransmitters as growth regulatory signals: role of receptors and second messengers. Trends Neurosci. 16:1993;233-240.
25. Lauder J.M., Han V.K., Henderson P., Verdoorn T., Towle A.C. Prenatal ontogeny of the GABAergic system in the rat brain: an immunocytochemical study. Neuroscience. 19:1986;465-493.
26. Laurie D.J., Seeburg P.H., Wisden W. The distribution of 13 GABAA receptor subunit mRNAs in the rat brain: II. Olfactory bulb and cerebellum. J. Neurosci. 12:1992;1063-1076.
27. Laurie D.J., Wisden W., Seeburg P.H. The distribution of thirteen GABAA receptor subunit mRNAs in the rat brain: III. Embryonic and postnatal development. J. Neurosci. 12:1992;4151-4172.
28. Lipton S.A., Kater S.B. Neurotransmitter regulation of neuronal outgrowth, plasticity and survival. Trends Neurosci. 12:1989;265-270.
29. Liu J., Morrow A.L., Devaud L., Grayson D.R., Lauder J.M. GABAA receptors mediate trophic effects of GABA on embryonic brainstem monoamine neurons in vitro. J. Neurosci. 17:1997;2420-2428.
30. Llinas R., Hillmann D.E. Physiological and morphological organization of the cerebellar circuits in various vertebrates. Llinas R. Neurobiology of Cerebellar Evolution and Development. 1969;43-73 Am. Med. Ass, Chicago.
31. Llinas R., Walton K.D. Cerebellum. Shepherd G.M. The Synaptic Organization of the Brain. 1990;214-245 Oxford Univ. Press, Oxford.
32. LoTurco J.J., Owens D.F., Heath M.J., Davis M.B., Kriegstein A.R. GABA and glutamate depolarize cortical progenitor cells and inhibit DNA synthesis. Neuron. 15:1995;1287-1298.
33. Ma W., Barker J.L. Complementary expressions of transcripts encoding GAD67 and GABAA receptor alpha 4, beta 1, and gamma 1 subunits in the proliferative zone of the embryonic rat central nervous system. J. Neurosci. 15:1995;2547-2560.
34. Macdonald R.L., Olsen R.W. GABAA receptor channels. Annu. Rev. Neurosci. 17:1994;569-602.
35. McCarthy M.M., Auger A.P., Perrot-Sinal T.S. Getting excited about GABA and sex differences in the brain. Trends Neurosci. 25:2002;307-312.
36. McKernan R.M., Whiting P.J. Which GABAA-receptor subtypes really occur in the brain? Trends Neurosci. 19:1996;139-143.
37. Mehta A.K., Ticku M.K. An update on GABAA receptors. Brain. Res. Brain Res. Rev. 29:1999;196-217.
38. Mellor J.R., Merlo D., Jones A., Wisden W., Randall A.D. Mouse cerebellar granule cell differentiation: electrical activity regulates the GABAA receptor alpha 6 subunit gene. J. Neurosci. 18:1998;2822-2833.
39. Miale I.L., Sidman R.I. An autoradiographic analysis of histogenesis in the mouse cerebellum. Exp. Neurol. 4:1961;277-296.
40. Mitchell C.K., Redburn D.A. GABA and GABA-A receptors are maximally expressed in association with cone synaptogenesis in neonatal rabbit retina. Brain Res. Dev. Brain Res. 95:1996;63-71.
41. Moss S.J., Smart T.G. Constructing inhibitory synapses. Nat. Rev. Neurosci. 2:2001;240-250.
42. Mugnaini E., Forstronen P.F. Ultrastructural studies on the cerebellar histogenesis: I. Differentiation of granule cells and development of glomeruli in the chick embryo. Z. Zellforsch Mikrosk. Anat. 77:1967;115-143.
43. Olsen R.W., Avoli M. GABA and epileptogenesis. Epilepsia. 38:1997;399-407.
44. Olsen R.W., Homanics G.E. Function of GABAA receptors. Martin D.L., Olsen R.W. GABA in the Nervous System: the View at Fifty years. 2000;P81-P96 Lippincott Williams and Wilkins, Philadelphia.
45. Owens D.F., Kriegstein A.R. Is there more to GABA than synaptic inhibition? Nat. Rev. Neurosci. 3:2002;715-727.
46. Palay S.L., Chan-Palay V. Cerebellar Cortex, Cytology and Organization. 1974;Springer, Berlin. 348 pp.
47. Perkins K.L., Wong R.K. The depolarizing GABA response. Can. J. Physiol. Pharmacol. 75:1997;516-519.
48. Persohn E., Malherbe P., Richards J.G. Comparative molecular neuroanatomy of cloned GABAA receptor subunits in the rat CNS. J. Comp. Neurol. 326:1992;193-216.
49. Poulter M.O., Barker J.L., O'Carroll A.M., Lolait S.J., Mahan L.C. Differential and transient expression of GABAA receptor alpha-subunit mRNAs in the developing rat CNS. J. Neurosci. 12:1992;2888-2900.
50. Rakic P. Mechanisms of neuronal migration in developing cerebellar cortex. Edelman G.E., Cowan W.M., Gall E. Molecular Basis of Neural Development. 1985;139-160 Wiley, New York.
51. Ramon y Cajal S. Histologie du System Nerveux de l'Homme et des Vertebres. vol. 2:1911;Malonine, Paris.
52. Rohrbough J., Spitzer N.C. Regulation of intracellular Cl- levels by Na(+)-dependent Cl-cotransport distinguishes depolarizing from hyperpolarizing GABAA receptor-mediated responses in spinal neurons. J. Neurosci. 16:1996;82-91.
53. - ion channels exhibit heterogeneous channel properties. Eur. J. Neurosci. 10:1998;1771-1783.
54. Sidman R., Rakic P. Development of the human central nervous system. Haymaker W., Adams R.D. Histology and Histopathology of the Nervous System. 1982;3-145 Springfield, Thomas.
55. Sieghart W. Structure and pharmacology of gamma-aminobutyric acidA receptor subtypes. Pharmacol. Rev. 47:1995;181-234.
56. Spoerri P.E. Neurotrophic effects of GABA in cultures of embryonic chick brain and retina. Synapse. 2:1988;11-22.
57. Takayama C., Inoue Y. Normal formation of the postsynaptic elements of GABAergic synapses in the reeler cerebellum. Brain Res. Dev. Brain Res. 145:2003;197-211.
58. Thompson C.L., Pollard S., Stephenson F.A. Developmental regulation of expression of GABAA receptor alpha 1 and alpha 6 subunits in cultured rat cerebellar granule cells. Neuropharmacology. 35:1996;1337-1346.
59. Van Eden C.G., Mrzljak L., Voorn P., Uylings H.B. Prenatal development of GABA-ergic neurons in the neocortex of the rat. J. Comp. Neurol. 289:1989;213-227.
60. Varju P., Katarova Z., Madarasz E., Szabo G. GABA signalling during development: new data and old questions. Cell Tissue Res. 305:2001;239-246.
61. Wang J.B., Kofuji P., Fernando J.C., Moss S.J., Huganir R.L., Burt D.R. The alpha 1, alpha 2, and alpha 3 subunits of GABAA receptors: comparison in seizure-prone and-resistant mice and during development. J. Mol. Neurosci. 3:1992;177-184.
62. Wolff J.R., Joo F., Kasa P. Modulation by GABA of neuroplasticity in the central and peripheral nervous system. Neurochem Res. 18:1993;453-461.
63. Yuasa S. Bergmann glial development in the mouse cerebellum as revealed by tenascin expression. Anat. Embryol. (Berl.). 194:1996;223-234.