Survival and mitogenesis of neuroepithelial cells are influenced by noradrenergic but not cholinergic innervation in cultured embryonic rat neopallium

Brain Research

Volumn 853, Issue 2, 2000, Pages 227-235

  Popovik, Elvira ^a   Haynes, Laurence W ^a  

^a UNIVERSITY OF BRISTOL   (United Kingdom)

Author keywords

Apoptosis; Cholinergic; Locus coeruleus; Neopallium; Neuroepithelium; Noradrenergic

Indexed keywords

DOPAMINE BETA MONOOXYGENASE;

ANIMAL TISSUE; APOPTOSIS; ARTICLE; COCULTURE; DENERVATION; EMBRYO; EMBRYO DEVELOPMENT; FOREBRAIN; IMMUNOCYTOCHEMISTRY; IN VITRO STUDY; NEUROEPITHELIUM; NONHUMAN; NORADRENERGIC SYSTEM; PARASYMPATHETIC INNERVATION; PRIORITY JOURNAL; RAT;

ACETYLCHOLINE; ADRENERGIC ALPHA-ANTAGONISTS; ANIMALS; APOPTOSIS; AXONS; CELL DIFFERENTIATION; CELL DIVISION; CELL SURVIVAL; CELLS, CULTURED; COCULTURE TECHNIQUES; DOPAMINE BETA-HYDROXYLASE; EPITHELIAL CELLS; IMMUNOHISTOCHEMISTRY; LIGANDS; NEOCORTEX; NERVE FIBERS; NERVE REGENERATION; NEURONS; NOREPINEPHRINE; PONS; RATS; RECEPTORS, ADRENERGIC, ALPHA-1; RECEPTORS, ADRENERGIC, ALPHA-2;

EID: 0033987722     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(99)02242-8     Document Type: Article

References (41)

1. Armstrong D.M., Bruce G., Hersh L.B., Gage F.H. Development of cholinergic neurons in the septal/diagonal band complex of the rat. Dev. Brain Res. 36:1987;249-256.
2. Behar T.N., Scott C.A., Greene C.L., Wen X., Smith S.V., Maric D., Liu Q.-Y., Coltona, Barker J.L. Glutamate acting at NMDA receptors stimulates embryonic cortical neuronal migration. J. Neurosci. 19:1999;4449-4461.
3. Blaschke A.J., Staley K., Chun J. Widespread programmed cell death in proliferative and postmitotic regions of the fetal cerebral cortex. Development. 122:1996;1165-1174.
4. Caviness V.S. Jr., Korde M.G. Monoaminergic afferents to the neocortex: a developmental histofluorescence study in normal and Reeler mouse embryos. Brain Res. 209:1981;1-9.
5. Chen S.H., Lin F., Iismaa S., Lee K.N., Birkbichler P.J., Graham R.M. Alpha(1)-adrenergic receptor signaling via G(h) is subtype-specific and independent of its transglutaminase activity. J. Biol. Chem. 271:1996;32385-32391.
6. Cruise J.L., Keith A.H., Michalkopoulos G.K. Induction of DNA synthesis in cultured rat hepatocytes through stimulation of α1 adrenoreceptors by norepinephrine. Science. 227:1985;749-751.
7. Dori I., Parnavelas J.G. The cholinergic innervation of the rat cerebral cortex shows two distinct phases in development. Exp. Brain Res. 76:1989;417-423.
8. Falck B., Hillarp A., Thieme G., Torp A. Fluorescence of catecholamines and related compounds condensed with formaldehyde. J. Histochem. Cytochem. 10:1962;348-354.
9. L Felten D., Hallman H., Jonsson G. Evidence for a neurotrophic role of noradrenaline neurons in the postnatal development of rat cerebral cortex. J. Neurocytol. 11:1982;119-135.
10. Ferri R.T., Levitt P. Regulation of regional differences in the differentiation of cerebral cortical neurons by EGF family-matrix interactions. Development. 121:1995;1151-1160.
11. G.A. Foster, Chemical neuroanatomy of the prenatal rat brain. Oxford, 1998.
12. h/type 2 transglutaminase following catecholamine deprivation is associated with depression of adrenoreceptor signal transduction in cultured ventricular zone germinal cells. Brain Res. 788:1998;95-103.
13. Golden G.S. Prenatal development of the biogenic amine systems of the mouse brain. Dev. Biol. 33:1973;300-311.
14. Hanley M.R. Peptide regulatory factors in the nervous system. Lancet. 1(8651):1989;1373-1376.
15. Hohman C.F., Brooks A.C., Coyle J.T. Neonatal lesions of the basal forebrain neurons result in abnormal cortical development. Dev. Brain Res. 42:1988;253-264.
16. Kuida K., Zheng T.S., Na S., Kuan C., Yang D., Karasuyama H., Rakic P., Flavell R.A. Decreased apoptosis in the brain and premature lethality in CPP-32-deficient mice. Nature. 384:1996;368-372.
17. Lauder, Bloom F.E. Ontogeny of monoamine neurons in the locus coeruleus, raphe nuclei and substantia nigra of the rat. J. Comp. Neurol. 155:1974;469-482.
18. Lauder J.M. Neurotransmitters as growth regulatory signals: role of receptors and second messengers. Trends Neurosci. 16:1993;2-8.
19. Lavdas A.A., Blue M.E., Lincoln J., Parnavelas J.G. Serotonin promotes the differentiation of glutamate neurons in organotypic slice cultures of the developing cerebral cortex. J. Neurosci. 17:1997;7872-7880.
20. Levitt P., Moore R.Y. Noradrenaline neurone innervation of the neocortex in the rat. Brain Res. 139:1978;219-231.
21. Lidow M.S., Rakic P. Unique profiles of the alpha1-, alpha-2, and beta-adrenergic receptors in the developing cortical plate and transient embryonic zones of the rhesus monkey. J. Neurosci. 14:1994;4064-4078.
22. Lidow M.S., Rakic P. Neurotransmitter receptors in the proliferative zones of the developing primate occipital lobe. J. Comp. Neurol. 360:1995;393-402.
23. Lo Turco J.J., Owens D.F., Heath M.J.S., Davis M.B.E., Kriegstein A.R. GABA and glutamate depolarize cortical progenitor cells and inhibit DNA synthesis. Neuron. 15:1995;1287-1298.
24. Mount H.T.J., Dreyfus C.F., Black I.B. Muscarinic stimulation promotes cultured Pukinje cell survival: a role for acetylcholine in cerebellar development. J. Neurochem. 63:1994;2065-2073.
25. Nakaki T., Nakayama M., Yamamoto S., Kato R. alpha1-Adrenergic stimulation and beta2-adrenergic inhibition of DNA synthesis in vascular smooth muscle cells. Mol. Pharmacol. 37:1990;30-36.
26. Nyakas C., Buwalda B., Kramers R.J.K., Traber J., Luiten P.G.M. Postnatal development of hippocampal and neocortical cholinergic and serotonergic innervation in rat: effects of nitrite-induced perinatal hypoxia and nimodipine treatment. Neurosci. 59:1994;541-559.
27. L. Olson, A. Seiger, Early prenatal ontogeny of central monoamine neurons in the rat: fluorescence histochemical observations. Z. Anat. Entwicklungsgesch. 137, 301-306.
28. Onteniente B., Koenig N., Sievers J.et al. Structural and biochemical changes in rat cerebral cortex after neonatal 6-hydroxydopamine administration. Anat. Embryol. 159:1980;245-255.
29. Ostermann, Grunwald J., Wevers A., Lorke D.E., Reinhardt S., Maelicke A., Schroder H. Cellular expression of alpha4 subunit mRNA of the nicotinic acetylcholine receptor in the developing rat telencephalon. Neurosci. Lett. 192:1995;21-24.
30. Pabbathi V.K., Brennan H., Muxworthy A., Gill L., Holmes F.E., Vignes M., Haynes L.W. Catecholamine regulation of proliferation and survival in rat forebrain paraventricular germinal cells. Brain Res. 760:1997;22-33.
31. Parnavelas J.G., Blue M.E. The role of the noradrenergic system on the formation of synapses in the visual cortex of the rat. Dev. Brain Res. 3:1982;140-144.
32. Rakic P. Dividing up the neocortex. Science. 258:1992;1421-1422.
33. Rakic P., Lombroso P.J. Development of the cerebral cortex: I. Forming the cortical structure. Journal of the American Academy of Child and Adolescent Psychiatry. 37:1998;116-117.
34. Schlumpf M., Palacios J.M., Cortes R., Lichtensteiger W. Regional development of muscarinic cholinergic binding sites in the prenatal rat brain. Neuroscience. 45:1991;347-357.
35. Temple S., Qian X. bFGF, neurotrophins, and the control of cortical neurogenesis. Neuron. 15:1995;249-252.
36. Thomaidou D., Mione M.C., Cavanagh J.F.R., Parnavelas J.G. Apoptosis and its relation to the cell cycle in the developing cerebral cortex. J. Neurosci. 17:1997;1075-1085.
37. Wang F., Lidow M.S. α2A-adrenergic receptors are expressed by diverse cell types in the fetal primate cerebral wall. J. Comp. Neurol. 378:1997;493-507.
38. Winzer-Serhan U.H., Leslie F.M. Expression of α2A adrenoreceptors during rat neocortical development. J. Neurobiol. 38:1999;259-269.
39. q family. J. Biol. Chem. 267:1992;25798-25802.
40. Wyllie A.H., Kerr J.F.R., Currie A.R. Cell death: the significance of apoptosis. Int. Rev. Cytol. 68:1980;251-306.
41. Yan G.M., Lin S.Z., Irwin R.P., Paul S.M. Activation of muscarinic cholinergic receptors blocks apoptosis of cultured cerebellar granule neurons. Mol. Pharmacol. 47:1985;253-264.