Basic fibroblast growth factor (FGF-2) protects rat cochlear hair cells in organotypical culture from aminoglycoside injury

Journal of Cellular Physiology

Volumn 167, Issue 3, 1996, Pages 443-450

  Low, Wesley ^a,b   Dazert, Stefan ^a,b   Baird, Andrew ^c   Ryan, Allen F ^a,b,d  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c SCRIPPS RESEARCH INSTITUTE   (United States)

^d VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOGLYCOSIDE ANTIBIOTIC AGENT; BASIC FIBROBLAST GROWTH FACTOR; CANCER GROWTH FACTOR; EPIDERMAL GROWTH FACTOR; INTERLEUKIN 1BETA; NEOMYCIN; NERVE GROWTH FACTOR; RETINOIC ACID;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL DEGENERATION; COCHLEA; CONTROLLED STUDY; HAIR CELL; NONHUMAN; OTOTOXICITY; PRIORITY JOURNAL; RAT; SENSORY NERVE CELL; STEREOCILIUM;

ANIMALS; ANTI-BACTERIAL AGENTS; CELL SURVIVAL; EPIDERMAL GROWTH FACTOR; FIBROBLAST GROWTH FACTOR 2; HAIR CELLS; INTERLEUKIN-1; MICROSCOPY, CONFOCAL; NEOMYCIN; NERVE GROWTH FACTORS; ORGAN CULTURE TECHNIQUES; ORGAN OF CORTI; RATS; RATS, SPRAGUE-DAWLEY; TRANSFORMING GROWTH FACTOR ALPHA; TRETINOIN; TUMOR NECROSIS FACTOR-ALPHA;

ANIMALIA;

EID: 0029950145     PISSN: 00219541     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-4652(199606)167:3<443::AID-JCP8>3.0.CO;2-P     Document Type: Article

References (50)

1. Anderson, K.J., Dam, D., Lee, S., and Cotman, C.W. (1988) Basic fibroblast growth factor prevents death of lesioned cholinergic neurons in vivo. Nature, 332:360-361.
2. Baird, A. (1994a) Fibroblast growth factors: Activities and significance of non-neurotrophin neurotrophic growth factors. Curr. Opin. Neurobiol., 4:78-86.
3. Baird, A. (1994b) Potential mechanisms regulating the extracellular activities of basic fibroblast growth factor (FGF-2). Mol. Reprod. Dev., 39:43-48.
4. Basilico, C., and Moscatelli, D. (1992) The FGF family of growth factors and oncogenes. Adv. Cancer Res. 59:115-165.
5. Dreyer, D., Lagrange, A., Grothe, C., and Unsicker, K. (1989) Basic fibroblast growth factor prevents ontogenetic neuron death in vivo. Neurosci. Lett., 99:35-38.
6. Dulon, D., Kiel, H., Aurousseau, C., Erre, J. and Aran, J. (1993) Pharmacokinetics of gentamicin in sensory hair cells of the organ of Corti: rapid uptake and long term persistence. Comp. Rend. Acad. Sci., 316:682-687.
7. Faktorovich, E., Steinberg, R., Yasumura, D., Mattes, M., and LaVail, M.M. (1990) Photoreceptor degeneration in inherited retinal dystrophy delayed by basic fibroblast growth factor. Nature, 347:83-86.
8. Faktorovich, E., Steinberg, R., Yasumura, D., Mattes, M., and LaVail, M.M. (1992) Basic fibroblast growth factor and local injury protect photoreceptors from light damage in the rat. J. Neurosci., 12:3554-3567.
9. Forge, A. (1985) Outer hair cell loss and supporting cell expansion following chronic gentamicin treatment. Hearing Res. 19:171-182.
10. Forge, A., Li, L., Corwin, J.T., and Nevill, G. (1993) Ultrastructural evidence for hair cell regeneration in the mammalian inner ear. Science, 259:1616-1619.
11. Frenz, D., Liu, W., Williams, J., Hatcher, V., Galinvic-Schwartz, V., Flanders, K., and Van De Water, T. (1994) Induction of chondrogenesis: Requirement for synergistic interaction of basic fibroblast growth factor and transforming growth factor beta. Development, 120:415-424.
12. Friesel, R.E. and Maciag, T. (1995) Molecular mechanisms of angiogenesis: fibroblast growth factor signal transduction. Faseb J. 9:919-925.
13. Grothe, C., and Unsicker, K. (1992) Basic fibroblast growth factor in the hypoglossal system: Specific retrograde transport, trophic, and lesion-related responses. J. Neurosci. Res., 32:317-328.
14. Hase, M., Ariki, S., Kaji, K., and Hayashi, H. (1995) Classification of signals for blocking apoptosis in vascular endothelial cells. J. Biochem., 116:905-909.
15. Hawkins, J.E., and Engstrom, H. (1964) Effects of kanamycin on cochlear cytoarchitecture. Acta Otolaryngol., 188 (Suppl.):100-106.
16. Henley, C., Gerhardt, H.-J., and Schacht, J. (1987) Inhibition of ornithine decarboxylase by neomycin in-vitro. Brain Res. Bull., 19:695-698.
17. Hiel, H., Erre, J.P., Aurousseau, C., Bouali, R., Dulon, D. and Aran, J.M. (1993) Gentamicin uptake by cochlear hair cells precedes hearing impairment during chronic treatment. Audiol. 32:78-87.
18. Isacchi, A., Statuto, M., Chiesa, R., Bergonzoni, L., Rusnati, M., Sarmientos, P., Ragnotti, G. and Presta, M. (1991) A six-amino acid deletion in basic fibroblast growth factor dissociates its mitogenic activity from its plasminogen activator-inducing capacity. Proc. Natl. Acad. Sci. 88:2628-2632.
19. Koch, T. and Gloddek, B. (1991) Inhibition of adenylate-cyclase-coupled G protein complex by ototoxic diuretics and cis-platinum in the inner ear of the guinea pig. Eur. Arch. Oto-Rhino Laryngol., 248:459-464.
20. Lefebvre, P.P., Weber, T., Rigo, J.M., Staecker, H., Moonen, G., and Van De Water, T.R. (1992) Peripheral and central target-derived trophic factors effects on auditory neurons. Hearing Res., 58:185-192.
21. Luo, L., Koutnouyan H., Baird, A., and Ryan, A.F. (1993) Acidic and basic FGF mRNA expression in the adult and developing rat cochlea. Hearing Res., 69:182-193.
22. Malgrange, B., Lefebvre, P., Baron, H., Liu, W., Staecker, H., Van De Water, T., and Moonen, G. (1994) Transforming growth factor alpha (TGFa) acts with retinoic acid to protect auditory hair cells from aminoglycoside induced ototoxicity. Abstr. Assoc. Res. Otolaryngol., 77:138.
23. Matz, G. (1993) Aminoglycoside cochlear ototoxicity. Otolaryngol. Clin. N. Am., 26:705-712.
24. Meiteles, L.Z., and Raphael, Y. (1994) Scar formation in the vestibular sensory epithelium after aminoglycoside toxicity. Hearing Res., 79:26-38.
25. Mohammadi, M., Djonne, C., Li, W., Spivak, T., Honneger, A., Jaye, M., and Schlessinger, J. (1992) Point mutation in FGF receptor eliminates phospoinositide hydrolysis without affecting mitogenesis. Nature, 358:681-684.
26. Ornitz, D., and Leder, P. (1992) Ligand specificity and heparin dependence of fibroblast growth factor receptors 1 and 3. J. Biol. Chem., 267:16305-16311.
27. Otto, D., and Unsicker, K. (1990) Basic FGF reverses chemical and morphological deficits in the nigrostriatal system of MPTP-treated mice. J. Neurosci., 10:1912-1921.
28. Pedersen, A.D., Morton, J.I., and Trune, D.R. (1993) Inner ear basic fibroblast growth factor in CBA/J, C3H/HeJ, and autoimmune Palmerston North mice. Hearing Res., 66:253-259.
29. Pertovaara, L., Tienari, J., Vainikka, S., Partanen, J., Saksela, O., Lehtonen, E., and Alitalo, K. (1993) Modulation of fibroblast growth factor receptor expression and signaling during retinoic acid induced differentiation of Tera-2-teratocarcinoma. Biochem. Biophys. Res. Commun., 191:149-56.
30. Peters, K., Ornitz, D., Werner, S., and Williams, L. (1993) Unique expression patterns of the FGF receptor 3 gene during mouse organogenesis. Dev. Biol., 155:423-430.
31. Pirvola, U., Cao, Y., Oellig, C., Suoqiang, Z., Pettersson, R.F., and Ylikoski, Y. (1995) The site of action of neuronal acidic fibroblast growth factor is the organ of Corti of the rat cochlea. Proc. Natl. Acad. Sci. U.S.A., 92:9269-9273.
32. Raphael, Y., Athey, B.D., Wang, Y., Lee, M.K., and Altschuler, R.A. (1994) F-actin, tubulin and spectrin in the organ of Corti: Comparative distribution in different cell types and mammalian species. Hearing Res., 76:173-187.
33. Richardson, G.P., and Russel, I.J. (1991) Cochlear cultures as a model system for studying aminoglycoside induced ototoxicity. Hearing Res., 53:293-311.
34. Roth, B., and Bruns, V. (1992) Postnatal development of the rat organ of Corti. Anat. Embryol., 185:559-569.
35. Ryan, A., and Dallos, P. (1975) Effect of absence of cochlear outer hair cells on behavioural auditory threshold. Nature, 253:44-46.
36. Rybak, L.P. (1993) Therapeutic use of aminoglycosides in Meniere's disease. Otolaryngol. Clin. N. Am., 26:737-746.
37. Schacht, J. (1974) Interaction of neomycin with phosphoinositide metabolism in guinea pig inner ear and brain tissues. Ann. Otol. Rhinol. Laryngol., 83:613-618.
38. Schacht, J. (1986) Molecular mechanism of drug-induced hearing loss. Hearing Res., 22:297-304.
39. Schacht, J. (1993) Biochemical basis of aminoglycoside ototoxicity. Otolaryngol. Clin. N. Am., 26.845-856.
40. Schlessinger, J., and Ullrich, A. (1992) Growth factor signaling by receptor tyrosine kinases. Neuron, 9:383-391.
41. Sievers, J., Hausmann, B., Unsicker, K., and Berry, M. (1987) Fibroblast growth factors promote the survival of adult rat retinal ganglion cells after transection of the optic nerve. Neurosci. Lett., 76:157-162.
42. Sobkowicz, H.M., Loftus, J.M., and Slapnick, S.M. (1993) Tissue culture of the organ of Corti. Acta Otolaryngol., 502 (Suppl.):3-36.
43. Stone, J.S., Zirpel, L., Loppe, W.R., and Rubel, E.W. (1995) Aminoglycoside ototoxicity: Mechanisms of increased (CA2+) in avian cochlear hair cells in vitro and in vivo. Soc. Neurosci. Abatr., 21:397.
44. Thomas, J., Marion, M., and Hinojosa, R. (1992) Neomycin ototoxicity. Am. J. Otolaryngol., 13:54-55.
45. Thorne, P.R., Corlisle, L., Zajic, G., Schacht, J., and Altschuler, R.A. (1987) Differences in the distribution of F-actin in outer hair cells along the organ of Corti. Hearing Res., 30:253-265.
46. Van de Water, T.R., and Ruben, R.J. (1971) Organ culture of the mammalian inner ear. Acta Otolaryngol., 71:303-312.
47. Van de Water, T.R., and Ruben, R.J. (1974) Growth of the inner ear in organ culture. Ann. Otol. Rhinol. Laryngol., 83 (Suppl. 14):1-16.
48. Walike, P., Cowan, W.M., Ueno, N., Baird, A., and Guillemin, R. (1986) Fibroblast growth factor promotes survival of dissociated hippocampal neurons and enhances neurite extension. Proc. Natl. Acad. Sci. U.S.A., 83:3012-3016.
49. Warchol, M.E., Lambert, P.R., Goldstein, B.J., Forge, A., and Corwin, J.T. (1993) Regenerative proliferation in inner ear sensory epithelia from adult guinea pigs and humans. Science, 259:1619-1622.
50. Yasuda, T., Grinspan, J., Stern, J., Franceschini, B., Bannerman, P., and Pleasure, D. (1995) Apoptosis occurs in the oligodendroglial lineage, and is prevented by basic FGF. J. Neurosci. Res., 40:306-317.