Peptide growth factors but not ganglioside protect against excitotoxicity in rat retinal neurons in vitro

Brain Research

Volumn 767, Issue 2, 1997, Pages 279-288

  Heidinger, Valérie ^a   Hicks, David ^a   Sahel, José ^a   Dreyfus, Henri ^a  

^a UNIVERSITY HOSPITAL OF STRASBOURG   (France)

Author keywords

Excitatory amino acid; Excitotoxicity; Ganglioside; Growth factor; Retinal neuron

Indexed keywords

BASIC FIBROBLAST GROWTH FACTOR; EPIDERMAL GROWTH FACTOR; GANGLIOSIDE; GROWTH FACTOR;

ANIMAL TISSUE; ARTICLE; CELL PROTECTION; HYPOGLYCEMIA; IN VITRO STUDY; NERVE DEGENERATION; NERVE FIBER GROWTH; NERVE INJURY; NEUROTRANSMITTER RELEASE; NONHUMAN; PRIORITY JOURNAL; RETINA NERVE CELL; SYNAPTIC TRANSMISSION; TISSUE DISTRIBUTION;

ANIMALS; CELL SURVIVAL; CELLS, CULTURED; EPIDERMAL GROWTH FACTOR; EXCITATORY AMINO ACIDS; FIBROBLAST GROWTH FACTOR 2; G(M1) GANGLIOSIDE; GROWTH SUBSTANCES; KAINIC ACID; NEURONS; NEUROPROTECTIVE AGENTS; NEUROTOXINS; PHOTORECEPTORS; RATS; RATS, WISTAR; RETINA;

EID: 0030777157     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(97)00605-7     Document Type: Article

References (71)

1. Abe K., Saito H. Protective effect of epidermal growth factor on glutamate neurotoxicity in cultured cerebellar neurons. Neurosci. Res. 14:1992;117-123.
2. Abrams L., Politi L.E., Adler R. Differential susceptibility of isolated mouse retinal neurons and photoreceptors to kainic acid toxicity. Invest. Ophthalmol. Vis. Sci. 30:1989;2300-2308.
3. Adler R. Preparation, enrichment, and growth of purified cultures of neurons and photoreceptors from chick embryos and from normal and mutant mice. Methods Neurosci. 2:1990;134-150.
4. Anchan R.M., Reh T.A., Angello J., Balliet A., Walker M. EGF and TGF-alpha stimulate retinal neuroepithelial cell proliferation in vitro. Neuron. 6:1991;923-936.
5. Anderson K.J., Dam D., Lee S., Cotman C.W. Basic fibroblast growth factor prevents death of lesioned cholinergic neurons in vivo. Nature. 332:1988;360-361.
6. Baird A., Esch F., Mormede P., Ueno N., Ling N., Bohlen P., Ying S.Y., Wehrenberg W.B., Guillemin R. Molecular characterization of fibroblast growth factor: distribution and biological activities in various tissues. Recent Prog. Horm. Res. 42:1986;143-152.
7. Barnstable C.J. Immunological studies of the diversity and development of the mammalian visual system. Immunol. Rev. 100:1987;47-78.
8. Barnstable C.J. Glutamate and GABA in retinal circuitry. Curr. Op. Neurobiol. 3:1993;520-525.
9. Bouvier M., Szatkowski M., Amato A., Attwell D. The glial cell glutamate uptake carrier countertransports pH-changing anions. Nature. 360:1992;471-474.
10. Burgess W., Macaig T. The heparin-binding (fibroblast) growth factor family of proteins. Annu. Rev. Biochem. 58:1989;575-606.
11. Caprioli J., Kitano S., Morgan J.E. Hyperthermia and hypoxia increase tolerance of retinal ganglion cells to anoxia and excitotoxicity. Invest. Ophthalmol. Vis. Sci. 37:1996;2376-2381.
12. Carpenter G., Cohen S. Epidermal growth factor. Annu. Rev. Biochem. 48:1979;193-216.
13. Cheng B., Mattson M.P. NGF and bFGF protect rat hippocampal and human cortical neurons against hypoglycemic damage by stabilizing calcium homeostasis. Neuron. 7:1991;1031-1041.
14. Choi D.W. Glutamate neurotoxicity and diseases of the nervous system. Neuron. 1:1988;623-634.
15. Collazo D., Takahashi H., McKay R.D.G. Cellular targets and trophic functions of neurotrophin-3 in the developing rat hippocampus. Neuron. 9:1992;643-656.
16. Daniotti J.L., Landa C.A., Rösner H., Maccioni J.F. Adult rat retina interneurons synthetize GD3: GD3 expression by these cells is regulated by cell-cell interactions. J. Neurochem. 59:1992;107-117.
17. Dräger U.C., Edwards D.L., Barnstable C.J. Antibodies against filamentous components in discrete cell types of the mouse retina. J. Neurosci. 4:1984;2025-2042.
18. Dreyfus H., Urban P.F., Edel-Harth S., Mandel P. Developmental patterns of gangliosides and phospholipids in chick retina and brain. J. Neurochem. 25:1975;245-250.
19. Dreyfus H., Guérold B., Fontaine V., Hicks D. Simplified ganglioside profile of photoreceptors compared to other retinal neurons. Invest. Ophthalmol. Vis. Sci. 37:1996;574-585.
20. Facci L., Leon A., Skaper S.D. Excitatory amino acid neurotoxicity in cultured retinal neurons: involvement of N-methyl-D-aspartate (NMDA) and non-NMDA receptors and effect of ganglioside GM1. J. Neurosci. Res. 27:1990;202-210.
21. Faktorovich E.G., Steinberg R.H., Yasumura D., Matthes M.T., LaVail M.M. Photoreceptor degeneration in inherited retinal dystrophy delayed by bFGF. Nature. 347:1990;83-86.
22. Fassio J.B., Brockman E.B., Jumblatt M., Greaton C., Henry J.L., Geoghegan T.E., Barr C., Schultz G.S. Transforming growth factor alpha and its receptor in neural retina. Invest. Ophthalmol. Vis. Sci. 30:1989;1916-1922.
23. Favaron M., Manev M., Alho H., Bertolino M., Ferret B., Guidotti A., Costa E. Gangliosides prevent glutamate and kainate neurotoxicity in primary neuronal cultures of neonatal rat cerebellum and cortex. Proc. Natl. Acad. Sci. USA. 85:1988;7351-7355.
24. M. Favaron, H. Manev, S. Vicini, A. Guidotti, E. Costa, Prevention of excitatory amino acid-induced neurotoxicity by natural and semisynthetic sphingolipids. In A. Guidotti (Ed.), Neurotoxicity of Excitatory Amino Acids, Raven Press, New York, 1990, pp. 243-258.
25. Fernandez-Sanchez M.T., Novelli A. Basic fibroblast growth factor protects cerebellar neurons in primary culture from NMDA and non-NMDA receptor mediated neurotoxicity. FEBS Lett. 335:1993;124-131.
26. Fisher D.A., Lakshmanan J. Metabolism and effects of epidermal growth factor and related growth factors in mammals. Endocr. Rev. 11:1990;418-442.
27. Fonnum F. Glutamate: a neurotransmitter in mammalian brain. J. Neurochem. 42:1984;1-11.
28. Freese A., Finklestein S.P., DiFiglia M. Basic fibroblast growth factor protects striatal neurons in vitro from NMDA-receptor mediated excitotoxicity. Brain Res. 575:1992;351-355.
29. Gospodarowicz D. Fibroblast and epidermal growth factors: their uses in vivo and in vitro in studies on cell functions and cell transplantation. Mol. Cell. Biochem. 25:1979;79-110.
30. Hakomori S.I. Glycosphingolipids in cellular interaction, differentiation and oncogenesis. Annu. Rev. Biochem. 50:1981;733-764.
31. Hamassaki-Britto D., Hermans-Borgmeyer I., Heinemann S., Hugues T.E. Expression of glutamate receptor genes in the mammalian retina: the localization of GluR1 through GluR7 mRNAs. J. Neurosci. 13:1993;1888-1898.
32. Harper J. Peritz «f» test: Basic program of a robust multiple comparision test for statistical analysis of all differences among group means. Compt. Biol. Med. 14:1984;437-445.
33. Hefti F., Hartikka J., Knusel B. Function of neurotrophic factors in the adult and aging brain and their possible use in the treatment of neurodegenerative diseases. Neurobiol. Aging. 10:1989;515-533.
34. Hicks D., Barnstable C.J. Different rhodopsin monoclonal antibodies reveal different binding patterns on developing and adult rat retina. J. Histochem. Cytochem. 35:1987;1317-1328.
35. D. Hicks, K. Bugra, B. Faucheux, J.-C. Jeanny, M. Laurent, F. Malecaze, F. Mascarelli, D. Raulais, Y. Cohen, Y. Courtois, Fibroblast growth factors in the retina. In N. Osborne and G. Chader (Eds.), Progress in Retinal Research, vol. 11, Pergamon, Oxford, 1991, pp. 333-374.
36. Hicks D., Courtois Y. Fibroblast growth factor stimulates photoreceptor differenciation in vitro. J. Neurosci. 12:1992;2022-2033.
37. Hugues T.E., Hermans-Borgmeyer I., Heinemann S. Differential expression of glutamate receptor genes (GluR1-5) in the rat retina. Vis. Neurosci. 8:1992;49-55.
38. Karpiak S.E., Li Y.S., Mahadik S.P. Gangliosides (GM1 and AGF2) reduce mortality due to ischemia: protection of membrane function. Stroke. 18:1987;184-187.
39. Kirschner P.B., Henshaw R., Weise J., Trubetskoy V., Finklestein S., Schultz J.B., Beal M.F. Basic fibroblast growth factor protects against excitotoxicity and chemical hypoxia in both neonatal and adult rats. J. Cereb. Blood Flow Metab. 15:1995;619-623.
40. Lazzaro A., Seren M.S., Koga T., Zanoni R., Schiavo N., Manev H. GM1 reduces infarct volume after focal cerebral ischemia. Exp. Neurol. 125:1994;278-285.
41. Ledeen R.W. Gangliosides of the neuron. Trends Neurosci. 8:1985;169-174.
42. Lucas D.R., Newhouse J.P. The toxic effect of sodium L-glutamate on the inner layers of the retina. Arch. Ophthalmol. 58:1957;193-201.
43. Maiese K., Boniece I., DeMeo D., Wagner J.A. Peptide growth factors protect against ischemia in culture by preventing nitric oxide toxicity. J. Neurosci. 13:1993;3034-3040.
44. Mascarelli F., Tassin J., Courtois Y. Effect of FGFs on adult bovine Müller cells: proliferation, binding and internalization. Growth Factors. 4:1991;81-95.
45. Mattson M.P., Rychlik B., Chu C., Christakos S. Evidence of calcium-reducing and excitoprotective roles for the calcium-binding protein calbindin-D28K in cultured hippocampal neurons. Neuron. 6:1991;41-51.
46. Mattson M.P., Lovell M.A., Furakawa K., Markesbery W.A. Neurotrophic factors attenuate glutamate-induced accumulation of peroxides, elevation of intracellular Ca2+ concentration, and neurotoxicity and increase antioxidant enzyme activities in hippocampal neurons. J. Neurochem. 65:1995;1740-1751.
47. Mayer M.L., Westbrook G.L. Cellular mechanisms underlying excitotoxicity. Trends Neurosci. 10:1987;59-61.
48. Meuillet E., Cremel G., Dreyfus H., Hicks D. Differential modulation of basic fibroblast and epidermal growth factor receptor activation by ganglioside GM3 in cultured retinal Müller glia. Glia. 17:1996;206-216.
49. Mohand-Said S., Weber M., Hicks D., Dreyfus H., Sahel J.A. Intravitreal injection of ganglioside GM1 after ischemia reduces retinal damage in rats. Stroke. 28:1997;617-622.
50. Morrison R.S., Sharma A., DeVellis J., Bradshaw R.A. Basic fibroblast growth factor supports the survival of cerebral cortical neurons in primary culture. Proc. Natl. Acad. Sci. USA. 83:1986;7537-7541.
51. Morrison R.S., Kornblum H.I., Leslie F.M., Bradshaw R.A. Trophic stimulation of cultured neurons from neonatal rat brain by epidermal growth factor. Science. 238:1987;72-75.
52. Müller F., Greferath U., Wässle H., Wisden W., Seeburg P. Glutamate receptor expression in the rat retina. Neurosci. Lett. 138:1992;179-182.
53. Nagai Y. Functional roles of gangliosides in bio-signalling. Behav. Brain Res. 66:1995;99-104.
54. Negishi K., Kato S., Teranishi T. Dopamine cells and rod bipolar cells contain protein kinase C-like immunoreactivity in some vertebrate retinas. Neurosci. Lett. 94:1988;247-252.
55. Olney J.W., Ho O.L., Rhee V. Cytotoxic effects of acidic and sulphur containing amino acids on the infant mouse central nervous system. Exp. Brain Res. 14:1971;61-76.
56. Otto D., Frotscher M., Unsicker K. Basic fibroblast growth factor and nerve growth factor administered in gel foam rescue media septal neurons after fimbria-fornix transection. J. Neurosci. Res. 22:1989;83-91.
57. Politi L.E., Adler R. Generation of enriched populations of cultured photoreceptor cells. Invest. Ophthalmol. Vis. Sci. 27:1986;656-665.
58. Puro D.G., Mano T. Modulation of calcium channels in human retinal glial cells by basic fibroblast growth factor: a possible role in retinal pathobiology. J. Neurosci. 11:1991;1873-1880.
59. Rothman S.M. The neurotoxicity of excitatory amino acids is produced by passive chloride influx. J. Neurosci. 5:1985;1483-1489.
60. Sarantis M., Attwell D. Glutamate uptake in mammalian retinal glia is voltage- and potassium-dependent. Brain Res. 516:1990;322-325.
61. Siesjö B.K. Pathophysiology and treatment of focal cerebral ischemia. I. Pathophysiology. J. Neurosurg. 77:1992;169-184.
62. Simon R.P., Chen J., Graham S.H. GM1 ganglioside treatment of focal ischemia: a dose-response and microdialysis study. J. Pharmacol. Exp. Ther. 265:1993;24-29.
63. Svennerholm L. Chromatographic separation of human brain gangliosides. J. Neurochem. 10:1963;613-623.
64. H. Tanihara, M. Inatani, Y. Honda, Growth factors and their receptors in the retina and pigmented epithelium. In N. Osborne and G. Chader (Eds.), Progress in Retinal and Eye Research, vol.16, Pergamon, Oxford, 1997, pp. 271-301.
65. Unoki K., LaVail M.M. Protection of the rat retina from ischemic injury by brain-derived neurotrophic factor, ciliary neurotrophic factor, and basic fibroblast growth factor. Invest. Ophthalmol. Vis. Sci. 35:1994;907-915.
66. Vorwerk C.K., Kreutz M.R., Dreyer E.B., Sabel B.A. Systemic L-kynurenine administration partially protects against NMDA, but not kainate-induced degeneration of retinal ganglion cells, and reduces visual discrimination deficits in adult rats. Invest. Ophthalmol. Vis. Sci. 37:1996;2382-2392.
67. Watkins J.C., Evans R.H. Excitatory amino acid and neurotransmitters. Annu. Rev. Pharmacol. 21:1981;165-204.
68. B.D. Watson, M.D. Ginsberg, Ischemic injury in brain: role of oxygen radical-mediated processes. In A.I. Barkai, N.G. Bazan (Eds.), Arachidonic Acid in the Nervous System. Physiological and Pathological Significance, vol. 559, Ann. NY Acad. Sci., 1989, pp. 269-281.
69. Weber M., Mohand-Said S., Hicks D., Dreyfus H., Sahel J.A. Monosialoganglioside GM1 reduces ischemia-reperfusion-induced injury in the rat retina. Invest. Ophthalmol. Vis. Sci. 37:1996;267-273.
70. Wen R., Song Y., Cheng T., Matthes M.T., Yasumura D., LaVail M.M., Steinberg R.H. Injury-induced upregulation of bFGF and CNTF mRNAS in the rat retina. J. Neurosci. 15:1995;7377-7385.
71. Zhang Y., Tatsuno T., Carney J.M., Mattson M.P. Basic FGF, NGF, and IGFs protect hippocampal and cortical neurons against iron-induced degeneration. J. Cereb. Blood Flow Metab. 13:1993;378-388.