GABA(A) receptor subunit expression in intrastriatal striatal grafts. Comparison between normal developing striatum and developing striatal grafts

Developmental Brain Research

Volumn 103, Issue 2, 1997, Pages 185-194

  Liste, I ^a   Caruncho, H J ^a   Guerra, M J ^a   Labandeira Garcia, J L ^a  

^a UNIVERSITY OF SANTIAGO DE COMPOSTELA   (Spain)

Author keywords

Development; GABA receptor; Graft; Pallidum; Striatum; Transplantation

Indexed keywords

4 AMINOBUTYRIC ACID; 4 AMINOBUTYRIC ACID A RECEPTOR; PHOSPHOPROTEIN DARPP 32; RECEPTOR SUBUNIT;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; BRAIN GRAFT; CONTROLLED STUDY; CORPUS STRIATUM; GENE EXPRESSION; GLOBUS PALLIDUS; IMMUNOHISTOCHEMISTRY; NONHUMAN; PRIORITY JOURNAL; RAT; SYNAPSE; TISSUE TRANSPLANTATION;

EID: 0030771539     PISSN: 01653806     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-3806(97)81794-4     Document Type: Article

References (68)

1. A receptor and improve water-maze learning in the rat. Brain Res. Bull. 33:1994;483-488.
2. Behar T., Schaffner A., Laing P., Hudson L., Komoly S., Barker J. Many spinal cord cells transiently express low molecular weight forms of glutamate acid decarboxylase during embryonic development. Dev. Brain Res. 72:1993;203-218.
3. Betz H. Glycine receptors: heterogeneous and widespread in the mammalian brain. Trends Neurosci. 14:1991;458-461.
4. Björklund A., Stenevi U., Schmidt R.H., Dunnett S.B., Gage F.H. Intracerebral grafting of neuronal cell suspensions. Acta Physiol. Scand., Suppl. 522:1983;1-75.
5. Brundin P., Isacson O., Björklund A. Monitoring of cell viability of embryonic CNS tissue and its use as criterion for intracerebral graft survival. Brain Res. 331:1985;251-259.
6. Brundin P., Isacson O., Gage F.H., Björklund A. Intrastriatal grafting of dopamine-containing neuronal cell suspensions: effects of mixing with target or non-target cells. Brain Res. 389:1986;77-84.
7. Campbell K., Kalén P., Lundberg C., Wictorin K., Rosengren E., Björklund A. Extracellular γ-aminobutyric acid levels in the rat caudate-putamen: Monitoring the neuronal and glial contribution by intracerebral microdialysis. Brain Res. 614:1993;241-250.
8. Campbell K., Kalén P., Lundberg C., Wictorin K., Mandel R.J., Björklund A. Characterization of GABA release from intrastriatal striatal transplants: dependence on host-derived afferents. Neuroscience. 53:1993;403-415.
9. Campbell K., Wictorin K., Björklund A. Neurotransmitter-related gene expression in intrastriatal striatal transplants: I. Phenotypical characterization of striatal and non-striatal graft regions. Neuroscience. 64:1995;17-33.
10. A receptor subunit expression in the rat neostriatum. Receptors Channels. 4:1996;85-92.
11. A receptor α1-subunit-immunopositive neurons in the rat striatum. Brain Res. 722:1996;185-189.
12. A receptor subunits in the anterior thalamus of the rat. Eur. J. Anat. 1:1996;43-50.
13. A receptor subunits in primary cultures of rat cerebellar granule cells. Neuroscience. 67:1995;583-593.
14. Cherubini E., Gaiarsa J.L., Ben-Ary Y. GABA: an excitatory transmitter in early postnatal life. Trends Neurosci. 14:1991;515-519.
15. Chronwall B., Wolff J.R. Prenatal and postnatal development of GABA-accumulating cells in the occipital neocortex of rat. J. Comp. Neurol. 190:1980;187-208.
16. D.J. Clarke, K. Wictorin, S.B. Dunnett and J.P. Bolam, Internal composition of striatal grafts: light and electron microscopy. in: G. Percheron, J.S. Mckenzie and J. Féger (Eds.), The Basal Ganglia. IV. New Ideas and Data on Structure and Function, Plenum, New York, 1994, pp. 189-196.
17. A receptor. Neuroscience. 40:1991;375-397.
18. Daubas P., Devillers-Thiery A., Geoffroy B., Martinez S., Bessis A., Changeux J.P. Differential expression of the neuronal acetylcholine receptor α2 subunit gene during chick brain development. Neuron. 5:1990;49-60.
19. Deckel A.W., Robinson R.G., Coyle J.T., Sanberg P.R. Reversal of long-term locomotor abnormalities in the kainic acid model of Huntington disease by day 18 fetal striatal implants. Eur. J. Pharmacol. 93:1983;287-288.
20. DiFiglia M., Schiff L., Deckel A.W. Neuronal organization of fetal striatal grafts in kainate- and sham-lesioned rat caudate nucleus: light- and electron-microscopic observations. J. Neurosci. 8:1988;1112-1130.
21. Dunnet S.B., Isacson O., Sirinathsinghji D.H.S., Clarke D.J., Björklund A. Striatal grafts in rats with unilateral striatal lesions. II. Recovery from dopamine dependent motor asymetry deficits in skilled paw reaching Neuroscience. 24:1988;813-820.
22. A receptors is recognized by two different monoclonal antibodies. Brain Res. 569:1992;57-62.
23. A/benzodiazepine receptor. J. Cell Biol. 110:1990;2043-2048.
24. Fishell G., Van der Kooy D. Pattern formation in the striatum: neurons with early projections to the substantia nigra survive the cell death period. J. Comp. Neurol. 312:1991;33-42.
25. Fiszman M.L., Behar T., Lange G.D., Smith S.V., Novotny E.A., Barker J.L. GABAergic cells and signals appear together in the early post-mitotic period of telencephalic and striatal development. Dev. Brain Res. 73:1993;243-251.
26. A-receptor heterogeneity in the adult rat brain: Differential regional and cellular distribution of seven major subunits. J. Comp. Neurol. 359:1995;154-194.
27. A-receptor subtypes during postnatal development: an immunohistochemical study. J. Neurosci. 14:1994;5302-5324.
28. Fritschy J.M., Benke D., Mertens S., Oertel W.H., Bachi T., Möhler H. Five subtypes of type A γ-aminobutyric acid receptors identified in neurons by double and triple immunofluorescence staining with subunit-specific antibodies. Proc. Natl. Acad. Sci. USA. 89:1992;6726-6730.
29. Graybiel A.M., Liu F.C., Dunnet S.B. Intrastriatal grafts derived from fetal striatal primordia: I. Phenotopy and modular organization. J. Neurosci. 9:1989;3250-3272.
30. Isacson O., Brundin P., Kelly P.A.T., Gage F.H., Björklund A. Functional neuronal replacement by grafted neurons in the ibotenic acid-lesioned striatum. Nature. 311:1984;458-460.
31. Isacson O., Brundin P., Gage F.H., Björklund A. Neural grafting in rat model of Huntington's disease: progressive neurochemical changes after neostriatal ibotenic lesions and striatal tissue grafting. Neuroscience. 16:1985;799-817.
32. Isacson O., Dawbarn D., Brundin P., Gage F.H., Eurson P.C., Björklund A. Neural grafting in rat model of Huntington disease: striosomal like organization of striatal grafts as revealed by immunocytochemistry and receptor autoradiography. Neuroscience. 22:1987;481-497.
33. Kita H., Kitai S.T. Glutamate decarboxylase immunoreactive neurons in rat neostriatum: their morphological types and populations. Brain Res. 447:1988;346-352.
34. Labandeira-Garcia J.L., Liste I., Tobio J.P., Rozas G., López-Martín E., Guerra M.J. Intrathalamic striatal grafts survive and affect circling behaviour in adult rats with excitotoxically lesioned striatum. Neuroscience. 68:1995;737-749.
35. Labandeira-Garcia J.L., Guerra M.J. Cortical stimulation induces fos expression in intrastriatal striatal grafts. Brain Res. 652:1994;87-97.
36. Labandeira-Garcia J.L., Tobio J.P., Guerra M.J. Comparison between normal developing striatum and developing striatal grafts using drug-induced Fos expression and neuron-specific enolase immunohistochemistry. Neuroscience. 60:1994;399-415.
37. Labandeira-Garcia J.L., Wictorin K., Cunningham E.T., Björklund A. Development of intrastriatal striatal grafts and their afferent innervation from the host. Neuroscience. 42:1991;407-426.
38. Lauder J.M., Han V.K.M., 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.
39. A receptor subunit mRNAs in the rat brain: III. Embryonic and postnatal development. J. Neurosci. 12:1992;4151-4172.
40. Lundberg C., Wictorin K., Björklund A. Retrograde degenerative changes in the substantia nigra pars compacta following an excitotoxic lesion of the striatum. Brain Res. 644:1994;205-212.
41. Ma W., Behar T., Barker J.L. Transient expression of GABA immunoreactivity in the developing rat spinal cord. J. Comp. Neurol. 235:1992;271-290.
42. A receptor channels. Ann. Rev. Neurosci. 17:1994;569-602.
43. Malosio M.L., Marqueze-Pouey B., Kuhse J., Betz H. Widespread expression of glycine receptor subunit mRNAs in the adult and developing rat brain. EMBO J. 10:1991;2401-2409.
44. Mayer E., Heavens R.P., Sirinathsinghji D.J.S. Autoradiographic localisation of D1 and D2 dopamine receptors in primordial striatal tissue grafts in rats. Neurosci. Lett. 109:1990;271-276.
45. McAllister J.P., Walker P.D., Zemanick M.C., Weber A.B., Kaplan L.I., Reynolds M.A. Morphology of embryonic neostriatal cell suspensions transplanted into adult neostriata. Dev. Brain Res. 23:1985;282-286.
46. Olsson M., Campbell K., Wictorin K., Björklund A. Projection neurons in fetal striatal transplants are predominantly derived from the lateral ganglionic eminence. Neuroscience. 69:1995;1169-1182.
47. Olsson M., Campbell K., Björklund A. Early specification of striatal projection neurons and interneuronal subtypes in transplants of the lateral or medial ganglionic eminence. Soc. Neurosci. Abstr. 22:1996;394.2.
48. Pakzaban P., Deacon T.W., Burns L.H., Isacson O. Increased proportion of acetylcholinesterase-rich zones and improved morphological integration in host striatum of fetal grafts derived from the lateral but not medial ganglionic eminence. Exp. Brain Res. 97:1993;13-22.
49. A receptor subunits in the rat CNS. J. Comp. Neurol. 326:1992;193-216.
50. Saji M., Reis D.J. Delayed transneuronal death of substantia nigra neurons prevented by gamma-aminobutyric acid agonist. Science. 235:1987;66-69.
51. A receptor subtypes. Pharmacol. Rev. 47:1995;181-234.
52. Sirinathsinghji D.J.S., Mayer E., Stam R., Fernandez J.M., Dunnet S.B. The expression of GAP-43 mRNA in developing embryonic striatal tissue grafts. NeuroReport. 4:1993;175-178.
53. Sirinathsinghji D.J.S., Dunnett S.B., Isacson O., Clarke D.J., Kendrick K., Björlund A. Striatal grafts in rats with unilateral neostriatal lesions: II. In vivo monitoring the GABA release in globus pallidus and substantia nigra. Neuroscience. 24:1988;803-811.
54. Snyder-Keller A., Constantini L.C. Glutamate receptor subtypes localize in patches in the developing striatum. Dev. Brain Res. 94:1996;246-250.
55. Somogyi P., Bolam J.P., Smith A.D. Monosynaptic cortical input and local axon collaterals of identified striatonigral neurons. A light and electron microscopic study using the Golgi-peroxidase transport-degeneration procedure. J. Comp. Neurol. 195:1981;567-584.
56. Taylor J., Docherty M., Gordon-Weeks P.R. Gabaergic growth cones: release of endogenous γ-aminobutyric acid precedes the expression of synaptic vesicle antigens. J. Neurochem. 54:1990;1689-1699.
57. Taylor J., Gordon-Weeks P.R. Developmental changes in the calcium dependency of γ-aminobutyric acid release from isolated growth cones: correlation with growth cone morphology. J. Neurochem. 53:1989;834-843.
58. Van Eden C.G., Mrzljak L., Voorn P., Uylings H.B.M. Prenatal development of GABA-ergic neurons in the neocortex of the rat. J. Comp. Neurol. 289:1989;213-227.
59. Walker P.D., McAllister J.P. Minimal connectivity between neostriatal transplants and the host brain. Brain Res. 425:1987;34-44.
60. Walker P.D., Chovanes G.I., McAllister J.I. Identification of acetylcholinesterase-reactive neurons and neuropil in neostriatal transplants. J. Comp. Neurol. 259:1987;1-12.
61. Wictorin K., Lagenaur C.F., Lund R.D., Björklund A. Efferents to the adult host brain from intrastriatal striatal mouse-to-rat as revealed by a mouse-neuron specific marker: time-course and tissue-type specifity. Eur. J. Neurosci. 3:1991;86-101.
62. Wictorin K., Ouimet C.C., Björklund A. Intrinsic organization and connectivity of intrastriatal transplants in rats as revealed by DARPP-32 immunohistochemistry: specificity of connections with the lesioned host brain. Eur. J. Neurosci. 1:1989;690-701.
63. Wictorin K., Simmerly R.B., Isacson O., Swanson L.W., Björklund A. Connectivity of striatal grafts implanted into ibotenic acid lesioned striatum: III. Efferent projecting graft neurons and their relation to host afferents within the grafts. Neuroscience. 30:1989;313-330.
64. Wictorin K., Björklund A. Connectivity of striatal grafts implanted into ibotenic acid lesioned striatum: II. Cortical afferents. Neuroscience. 30:1989;297-311.
65. Wictorin K., Isacson O., Fischer W., Nothias F., Peschanski M., Björklund A. Connectivity of striatal grafts implanted into ibotenic acid lesioned striatum: I. Subcortical afferents. Neuroscience. 27:1988;547-562.
66. A receptor subunit mRNAs in the rat brain: I. Telencephalon, diencephalon, mesencephalon. J. Neurosci. 12:1992;1040-1062.
67. Witzemann V., Barg B., Nishikawa Y., Sakmann B., Numa S. Differential regulation of muscle acetylcholine receptor γ and ε-subunit mRNAs. FEBS Lett. 223:1987;104-112.
68. 2+ influx in developing neocortex by excitatory and inhibitory neurotransmitters. Neuron. 6:1993;333-344.