Catecholaminergic regulation of proliferation and survival in rat forebrain paraventricular germinal cells

Brain Research

Volumn 760, Issue 1-2, 1997, Pages 22-33

  Pabbathi, Vijay K ^a   Brennan, Hannah ^a   Muxworthy, Anne ^a   Gill, Lukhbir ^a   Holmes, Fiona E ^a   Vignes, Michel ^a   Haynes, Laurence W ^a  

^a UNIVERSITY OF BRISTOL   (United Kingdom)

Author keywords

1 Adrenoreceptor; Apoptosis; Catecholamine; Cell culture; DNA synthesis; Ventricular zone

Indexed keywords

ALPHA 1 ADRENERGIC RECEPTOR; CATECHOLAMINE; CHLOROETHYLCLONIDINE; NORADRENALIN; PHENYLEPHRINE; PRAZOSIN;

ANIMAL CELL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; BINDING SITE; CALCIUM CELL LEVEL; CELL CULTURE; CELL PROLIFERATION; CELL SURVIVAL; CONCENTRATION RESPONSE; DNA SYNTHESIS; EMBRYO; FEMALE; GENE EXPRESSION; GERMINATION; IMMUNOHISTOCHEMISTRY; LIGAND BINDING; NEOCORTEX; NERVE ENDING; NEUROEPITHELIUM; NONHUMAN; PRIORITY JOURNAL; RAT; RECEPTOR BINDING; REGULATORY MECHANISM; STEM CELL; THALAMUS MIDLINE NUCLEUS;

ADRENERGIC ALPHA-ANTAGONISTS; ANIMALS; CATECHOLAMINES; CELL DIVISION; CELL SURVIVAL; CELLS, CULTURED; CLONIDINE; DOSE-RESPONSE RELATIONSHIP, DRUG; FEMALE; IMMUNOHISTOCHEMISTRY; PARAVENTRICULAR HYPOTHALAMIC NUCLEUS; PHENETHYLAMINES; PHENYLEPHRINE; PREGNANCY; PROSENCEPHALON; RADIOLIGAND ASSAY; RATS; RATS, WISTAR; STEM CELLS; TETRALONES;

EID: 0030841760     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(97)00272-2     Document Type: Article

References (53)

1. Allen T.J.G., Brown D.A. Detection and modulation of acetylcholine release from neurites of rat basal forebrain cells in culture. J. Physiol. 492:1996;453-466.
2. J. Altman and S.A. Bayer, Atlas of Prenatal Rat Brain Development, CRC, Boca Raton, FL, 1995.
3. Barochovsky O., Patel A.L. Effect of central nervous system-acting drugs in brain cell replication in vitro. Neurosci. Res. 27:1982;109-116.
4. Bayer S.A., Zhang X., Russo R.J., Altman J. Three-dimensional reconstructions of the developing forebrain in rat embryos. Neuroimage. 1:1994;296-307.
5. B. Berger, C. Verney and P.S. Goldman-Rakic, Prenatal monoaminergic innervation of the cerebral cortex: differences between rodents and primates. In I. Kostovic, S. Knezevic, H.M. Wisniewski and G.J. Spilich (Eds.), Neurodevelopment, Aging and Cognition, Birkhauser, Boston, MA, 1992, pp. 18-36.
6. Brennan H., Muxworthy A., Vignes M., Pabbathi V.K., Holmes F.E., Haynes L.W. Trophic control of survival and proliferation in cultured rat embryo forebrain germinal cells by α-adrenoreceptors. J. Physiol. 487:1995;44P.
7. Bristol J.A., Rhee S.G. Regulation of phospholipase C-β isozymes by G-proteins. Trends Endocrinol. Metab. 5:1994;402-406.
8. 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.
9. Caviness V.S., Takahashi T. Proliferative events in the cerebral ventricular zone. Brain Dev. 17:1995;159-163.
10. Chun J.J., Nakamura M.J., Shatz C.J. Transient cells of the developing mammalian telencephalon are peptide-immunoreactive neurons. Nature (London). 325:1987;617-620.
11. B adrenergic receptor. Biochem. Soc. Trans. 23:1995;121-125.
12. 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.
13. h protein is a signal mediator from α1-adrenoreceptor to a phospholipase C. J. Biol. Chem. 268:1993;27398-27405.
14. Ferrer I., Soriano E., Del Rio J.A., Alcantara S., Auladell C. Cell death and removal in the cerebral cortex during development. Progr. Neurobiol. 39:1992;1-43.
15. Fesus L., Thomazy V., Falus A. Searching for function of tissue transglutaminase; its possible involvement in biochemical pathway of programmed cell death. Adv. Expl. Biol. 231:1988;119-134.
16. Fraser A., McCarthy N., Evan E.I. The biochemistry of cell death. Curr. Opion. Neurobiol. 6:1996;71-80.
17. Freeman R.S., Estus S., Johnson E.M.S. Analysis of cell cycle-related gene expression in postmitotic neurons-selective induction of cyclin D1 during programmed cell death. Neuron. 12:1994;345-355.
18. Golden G.S. Prenatal development of the biogenic amine systems of the mouse brain. Dev. Biol. 33:1973;300-311.
19. 2+ in smooth muscle. Nature (London). 329:1987;333-335.
20. Herrup K., Busser J.C. The induction of multiple cell-cycle events precedes target-related neuronal death. Development. 121:1995;1183-1193.
21. Hosli E., Hosli L. Evidence for the existence of α and β-adrenoreceptors on neurones and glial cells of cultured rat central nervous system - an autoradiographic study. Neuroscience. 7:1982;2873-2881.
22. Kilpatrick T.J., Bartlett P.F. Cloned multipotential precursors from the mouse cerebrum require FGF-2, whereas glial restricted precursors are stimulated with either FGF-2 or EGF. J. Neurosci. 15:1995;3653-3661.
23. Kristt D.A. Development of cortical circuitry: quantitative ultrastructural analysis of putative monoaminergic synapses. Brain Res. 178:1979;69-88.
24. Levitt P., Moore R.Y. Development of the noradrenergic innervation of neocortex. Brain. Res. 162:1979;243-259.
25. Lidow M.S., Rakic P. Scheduling of monoamine neurotransmitter receptor expression in the primate neocortex during postnatal development. Cereb. Cortex. 2:1992;401-416.
26. Lidow M.S., Rakic P. Unique profiles of the α1, α2 and β-adrenergic receptors in the developing cortical plate and transient embryonic zones of the rhesus monkey. J. Neurosci. 14:1994;4064-4078.
27. Lipton S.A., Kater S.B. Neurotransmitter regulation of neuronal outgrowth, plasticity and survival. Trends Neurosci. 12:1989;265-270.
28. Lo A.C., Houenou L.J., Oppenheim R.W. Apoptosis in the nervous system: morphological features, methods, pathology and prevention. Arch. Histol. Cytol. 58:1995;139-149.
29. Lo Turco J.J., Blanton M.G., Kriegstein A.R. Initial expression and endogenous activation of NMDA channels in early neocortical development. J. Neurosci. 11:1991;792-799.
30. 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.
31. Meucci O., Scorziello A., Avallone A., Flrio T., Schettini G. α1B but not α1A adrenoreceptor activates calcium influx through the stimulation of a tyrosine kinase/phosphotyrosine pathway following noradrenaline-induced emptying of IP3 sensitive calcium stores in PC C13 rat thyroid cell line. Biochem. Biophys. Res. Commun. 209:1995;630-638.
32. Nakaki T., Nakayama N., Yamamoto S., Kato R. α1-Adrenergic stimulation and β2-adrenergic inhibition of DNA synthesis in vascular smooth muscle cells. Mol Pharmacol. 37:1989;30-36.
33. h: a GTP-binding protein with transglutaminase activity and receptor signaling function. Science. 264:1994;1593-1596.
34. L. Olson and A. Seiger, Early prenatal ontogeny of central monoamine neurons in the rat: fluorescence histochemical observations, Z. Anat. Entwicklgesch., 137, 301-316.
35. J.G. Parnavelas, G.C. Papadopoulos and M.E. Cavanagh, Changes in neurotransmitters during development. In A. Peters and E.C. Jones (Eds.), Cerebral Cortex, Vol. 7, Plenum, New York, NY, 1988. pp. 177-209.
36. Perry M.J.M., Mahoney S.-A., Haynes L.W. Transglutaminase C in cerebellar granule neurons: regulation and localization of substrate cross-linking. Neuroscience. 4:1995;1063-1076.
37. Refsnes M., Dajani O.F., Sandnes D., Thoresen G.H., Rottingen J.A., Iversen J.G., Christoffersen T. On the mechanisms of the growth-promoting effect of prostaglandins in hepatocytes - the relationship between DNA synthesis and signaling mediated by adenylate cyclase and phosphoinositide-specific phospholipase C. J. Cell Physiol. 164:1995;465-473.
38. Reynolds B.A., Tetzlaff W., Weiss S. A multipotent EGF-responsive striatal embryonic progenitor cell produces neurons and astrocytes. J. Neurosci. 12:1992;4564-4574.
39. Sadile A.G., Lambertidmello C., Cerbone A., Amoroso S., Annunziato L., Menna T., Buono C., Giuditta A. Adrenergic receptor systems and unscheduled DNA synthesis in rat brain. Brain Res. Bull. 37:1995;139-148.
40. Schlumpf M., Shoemaker W.J., Bloom F.E. Innervation of embryonic rat cerebral cortex by catecholamine-containing fibers. J. Comp. Neurol. 192(1980):1980;361-376.
41. Shaw C., Cameron L., March D., Cynader M., Zielinski B., Hendrickson A. Pre- and postnatal development of GABA receptors in Macaca monkey visual cortex. J. Neurosci. 11:1991;3943-3959.
42. Singh N.P., Stephens R.E. A novel technique for viable cell determinations. Stain Technol. 61:1986;315-318.
43. Slotkin T.A., Windh R., Whitmore W.L., Seidler F.J. Adrenergic control of DNA synthesis in developing rat brain regions: effects of intracisternal administration of isoproterenol. Brain Res. Bull. 21:1988;737-740.
44. Son J.H., Min N., Toh T.H. Early ontogeny of catecholaminergic cell lineage in brain and peripheral neurons monitored by tyrosine hydroxylase-lacZ transgene. Mol. Brain. Res. 36:1996;300-308.
45. Thomaidou D., Mione M.C., Parnavelas J.G. Apoptosis is associated with specific stages of the cell cycle in the subventricular zone of newborn rats. Brain Res. Assoc. Abstr. 12:1995;101.
46. Thomas S.A., Matsumoto A.M., Palmitier R.D. Noradrenaline is essential for mouse fetal development. Nature (London). 374:1995;643-646.
47. Vaccarino F.M., Schwartz M.L., Hartigan D., Leckman J.F. Basic fibroblast growth factor increases the number of excitatory neurons containing glutamate in the cerebral cortex. Cereb. Cortex. 5:1995;64-78.
48. Van Eden C.J., Mrzljak L., Voom P., Uylings H.B. Prenatal development of GABA-ergic neurons in the neocortex of the rat. J. Comp. Neurol. 289:1989;213-227.
49. Wallace J.A., Lauder J.M. Development of the serotonergic system in the rat embryo: an immunocytochemical study. Brain Res. Bull. 10:1983;459-479.
50. q family. J. Biol. Chem. 267:1992;25798-25802.
51. Yan G.M., Ni B., Weller M., Wood K.A., Paul S.M. Depolarization or glutamate receptor activation blocks apoptotic death of cultured cerebellar granule neurons. Brain Res. 656:1994;43-51.
52. 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. 47:1995;248-267.
53. Zhou Q.Y., Quaife C.J., Palmitier R.D. Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse foetal development. Nature (London). 374:1995;640-643.