Elongation of axons during regeneration involves retinal crystallin β b2 (crybb2)

Molecular and Cellular Proteomics

Volumn 6, Issue 5, 2007, Pages 895-907

  Liedtke, Thomas ^a   Schwamborn, Jens Christian ^a   Schröer, Uwe ^a   Thanos, Solon ^a  

^a UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBODY; CRYSTALLIN; CRYSTALLIN BETA B2; GREEN FLUORESCENT PROTEIN; NEURITE PROMOTING FACTOR; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; AUTOCRINE EFFECT; BRAIN NERVE CELL; CELL CULTURE; CONTROLLED STUDY; DEGENERATIVE DISEASE; EMBRYO; GENETIC TRANSFECTION; HIPPOCAMPUS; IMMUNOHISTOCHEMISTRY; IN VITRO STUDY; MOLECULAR CLONING; NERVE FIBER GROWTH; NERVE FIBER REGENERATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEOMICS; RAT; RETINA; RETINA GANGLION CELL; SUPERNATANT; TISSUE CULTURE; UPREGULATION;

AMINO ACID SEQUENCE; ANIMALS; AXONS; BETA-CRYSTALLIN B CHAIN; CALLITHRIX; CELL CULTURE TECHNIQUES; CELL LINE; CELLS, CULTURED; CULTURE MEDIA; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; GROWTH CONES; MOLECULAR SEQUENCE DATA; PROTEIN ISOFORMS; PROTEOMICS; RATS; RATS, SPRAGUE-DAWLEY; RETINA; RETINAL GANGLION CELLS; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION;

EID: 33947159103     PISSN: 15359476     EISSN: None     Source Type: Journal    
DOI: 10.1074/mcp.M600245-MCP200     Document Type: Article

References (55)

1. Ramon y Cajal, S. (1928) Degeneration and Regeneration of the Nervous System, Oxford University Press, New York
2. Caroni, P., and Schwab, M. E. (1988) Antibody against myelin-associated inhibitor of neurite growth neutralises non permissive substrate properties of CNS white matter. Neuron 1, 85-96
3. Davies, S. J., Fitch, M. T., Memberg, S. P., Hall, A. K., Raisman, G., and Silver, J. (1997) Regeneration of adult axons in white matter tracts of the central nervous system. Nature 390, 608-683
4. Chen, M. S., Huber, A. B., van der Haar, M. E., Frank. M, Schnell, L., Spillmann, A. A., Christ, F., and Schwab, M. E. (2000) Nogo-A is a myelin-associated neurite outgrowth inhibitor and an antigen for monoclonal antibody IN-1. Nature 403, 434-439
5. Mukhopadhyay, G., Doherty, P., Walsh, F. S., Crocker, P. R., and Filbin, M. T. (1994) A novel role for myelin associated glycoprotein as an inhibitor of axonal regeneration. Neuron 13, 757-767
6. McKerracher, L., David, S., Jackson, D. L., Kottis, V., Dunn, R.J., and Braun, P. E. (1994) Identification of myelin-associated glycoprotein as a major myelin-derived inhibitor of neurite growth. Neuron 13, 805-811
7. Moon, L. D. F., Asher, R. A., Rhodes, K. E., and Fawcett, J. W. (2001) Regeneration of CNS axons back to their target following treatment of adult rat brain with chondroitinase ABC. Nat. Neurosci. 4, 465-466
8. Wang, K. C., Koprivica, V., Kim, J. A., Sivasankaran, R., Guo, Y., Neve, R. L., and He, Z. (2002) Oligodendrocyte-myelin glycoprotein is a Nogo receptor ligand that inhibits neurite outgrowth. Nature 417, 941-944
9. Fournier, A. G., GrandPre, T., and Strittmatter, S. M. (2001) Identification of a receptor mediating Nogo-66 inhibition of axonal regeneration. Nature 409, 341-346
10. Domeniconi, M., Cao, Z., Spencer, T., Sivasankaran, R., Wang, K., Nikulina, E., Kimura, N., Cai, H., Deng, K., Gao, Y., He, Z., and Filbin, M. (2002) Myelin-associated glycoprotein interacts with the nogo66 receptor to inhibit neurite outgrowth. Neuron 35, 283
11. Liu, B. P., Fournier, A., GrandPre, T., and Strittmatter, S. M. (2002) Myelin-associated glycoprotein as a functional ligand for the Nogo66 receptor. Science 297, 1190-1193
12. Weibel, D., Cadelli, D., and Schwab, M. E. (1994) Regeneration of lesioned rat optic nerve fibers is improved after neutralization of myelin-associated neurite growth inhibitors. Brain Res. 642, 259-266
13. Lehman, M., Fournier, A., Selle-Navarro, I., Dergham, P., Sebok, A., Leclerc, N., Tigyi, G., and McKerracher, L. (1999) Inactivation of Rho signalling pathway promotes CNS axon regeneration. J. Neurosci. 19, 7537-7547
14. Fischer, D., He, Z., and Benowitz, L. I. (2004) Counteracting the Nogo receptor enhances optic nerve regeneration if retinal ganglion cells are in a active growth state. J. Neurosci. 24, 1646-1651
15. Vidal-Sanz, M., Bray, G. M., Villegas-Perez, M. P., Thanos, S., and Aguayo, A. J. (1987) Axonal regeneration and synapse formation in the superior colliculus by retinal ganglion cells in adult rat. J. Neurosci. 7, 2894-2909
16. Bahr, M., Vanselow, J, and Thanos, S. (1988) In vitro regeneration of adult rat ganglion cell axons from retinal explants. Exp. Brain Res. 73, 393-401
17. Goldberg, J. L., Espinosa, J. S., Xu, Y., Davidson, N., Kovacs, G. T., and Barres, B. A. (2002) Retinal ganglion cells do not extend axons by default: promotion by neurotrophic signalling and electrical activity. Neuron 33, 689-702
18. Leon, S., Yin, Y., Nguyen J, Irwin, N., and Benowitz, L. I. (2000) Lens injury stimulates axon regeneration in the mature rat optic nerve. J. Neurosci. 20, 4615-4626
19. Fischer, D., Heiduschka, P., and Thanos, S. (2000) Cataractogenic lens injury prevents traumatic ganglion cell death and promotes axonal regeneration both in vivo and in culture. Investig. Ophthalmol. Vis. Sci. 41, 3943-3954
20. Fischer, D., Heiduschka, P., and Thanos S. (2001) Lens-injury stimulated axonal regeneration throughout the optic pathway of adult rats. Exp. Neurol. 172, 257-272
21. Yin, Y., Cui, Q., Li, Y., Irwin, N., Fischer, D., Harvey, A. R., and Benowitz, L. I. (2003) Macrophage-derived factors stimulate optic nerve regeneration. J. Neurosci. 23, 2284-2293
22. Berry, M., Carlile, J., and Hunter, A. (1996) Peripheral nerve explants grafted into the vitreous body of the eye promote the regeneration of retinal ganglion cell axons severed in the optic nerve. J. Neurocytol. 25, 147-170
23. Li, Y., Irwin, N., Yin, Y., Lanser, M., and Benowtiz, L. I. (2003) Axon regeneration in goldfish and rat retinal ganglion cells: differential responsiveness to carbohydrates and camp. J. Neurosci. 23, 7830-7838
24. Lorber, B., Berry, M., Logan, A., and Tonge, D. (2002) Effect of lens lesion on neurite outgrowth of retinal ganglion cells in vitro. Mol. Cell. Neurosci. 21, 301-311
25. Stupp, T., Pavlidis, M., Busse, H., and Thanos, S. (2005) Lens epithelium supports axonal regeneration of retinal ganglion cells in a coculture model in vitro. Exp. Eye Res. 81, 530-538
26. Fischer, D., Petkova, V., Thanos, S., and Benowitz, L. I. (2004) Switching mature retinal ganglion cells to a robust growth state in vivo: gene expression and synergy with RhoA inactivation. J. Neurosci. 24, 8726-8740
27. Krishnamoorthy, R. R., Agarwal, P., Prasanna, G., Vopat, K., Lambert, W., Sheedlo, H. J., Pang, I. H., Shade, D., Wordinger, R. J., Yorio, T., Clark, A. F., and Agarwal, N. (2001) Characterization of a transformed rat retinal ganglion cell line. Brain Res. Mol. Brain Res. 86, 11-112
28. Schwamborn, J. C., and Puschel, A. W. (2004) The sequential activity of the GTPases Rap1B and Cdc42 determines neuronal polarity. Nat. Neurosci. 7, 923-929
29. Steuer, H., Jaworski, A., Stoll, D., and Schlosshauer, B. (2004) In vitro model of the outer blood-retina barrier. Brain Res. Brain Res. Protoc. 13, 26-36
30. König, S., Schmidt, O., Rose, K., Thanos, S., Besselmann, M., and Zeller, M. (2003) Sodium dodecyl sulfate versus acid-labile surfactant gel electrophoresis: comparative proteomic studies on rat retina and mouse brain. Electrophoresis 24, 751-756
31. Najak, S., Sashidhar, R. B., and Bhat, K. S. (2002) Development of an immunoanalytical method for the detection of β- and γ-crystallins and anti-crystallin antibodies. A molecular biomarker for cataract. Indian J. Ophthalmol. 50, 41-48
32. Wang, S. W., Gan, L., Martin, S. E., and Klein, W. H. (2000) Abnormal polarization and axonal outgrowth in retinal ganglion cells lacking POU-domain transcription factor Brn-3b. Mol. Cell. Neurosci. 16, 141-156
33. Srivastava, O. P., Kirk, M. C., and Srivastava, K. (2004) Characterization of covalent multimers of crystallins in aging human lenses. J. Biol. Chem. 279, 10901-10909
34. Wistow, G. (1993) Lens crystallins: gene recruitment and evolutionary dynamism. Trends Biochem. Sci. 18, 301-306
35. Grew, J. (1997) The crystallins: Genes, proteins and diseases. Biol. Chem. 378, 1331-1348
36. Sax, C. M., and Piatigorsky, J. (1994) Expression of the α-crystallin/ small heat-shock protein/molecular chaperone genes in the lens and other tissues. Adv. Enzymol. Relat. Areas Mol. Biol. 69, 155-201
37. Berman, E. R. (1994) Biochemistry of cataracts, in Pathology of Ocular Diseases: a Dynamic Approach (Garner, A. and Klintworth, G. K., eds) pp. 533-590, Marcel Dekker Inc., New York
38. Klemenz, R., Frohli, E., Steiger, R. H., Schafer, R., and Aoyama, A. (1991) α-B-Crystallin is a small heat shock protein. Proc. Natl. Acad. Sci. U. S. A. 88, 3652-3656
39. Xi, J., Farjo, R., Yoshida, S., Kern, T. S., Swaroop, A., and Andley, U. P. (2003) A comprehensive analysis of the expression of crystallins in mouse retina. Mol. Vis. 9, 410-419
40. Horwitz, J. (1992) α-Crystallin can function as a molecular chaperone. Proc. Natl. Acad. Sci. U. S. A. 89, 10449-10453
41. De Jong, W. W., Leunissen, J. A., and Voorter, C. E. (1993) Evolution of the α-crystallin/small heat-shock protein family. Mol. Biol. Evol. 10, 103-126
42. Andley, U. P., Mathur, S., Griest, T. A., and Petrash, J. M. (1996) Cloning, expression, and chaperone-like activity of human α-crystallin. J. Biol. Chem. 271, 31973-31980
43. Clayton, R. M., Thomson, I., and de Pomerai, D. I. (1979) Relationship between crystallin mRNA expression in retina cells and their capacity to re-differentiate into lens cells. Nature 282, 628-629
44. Head, M. W., Sedowofia, K., and Clayton, R. M. (1995) β B2-crystallin in the mammalian retina. Exp. Eye Res. 61, 423-428
45. Jones, S. E., Jomary, C., Grist, J., Thomas, M. R., and Neal, M. J. (1998) Expression of αβ-crystallin in a mouse model of inherited retinal degeneration. Neuroreport 19, 4161-4165
46. Vasquez-Ghona, F., Song, B. G., and Geisert, E. E., Jr. (2004) Temporal changes in gene expression after injury in the rat retina. Investig. Ophthalmol. Vis. Sci. 45, 2737-2746
47. Liu, C., Asgnerie, N., Lemakin, A., Parde, J., Ogun, O., and Benedek, G. B. (1996) Phase separation in aqueous solutions of lens γ-crystallins: special role of γs. Proc. Natl. Acad. Sci. U. S. A. 93, 377-382
48. Liang, P., and MacRae, T. H. (1997) Molecular chaperones and the cytoskeleton. J. Cell Sci. 110, 1431-1440
49. Coop, A., Wiesmann, K. E., and Crabbe, M. J. (1998) Translocation of β crystallin in neural cells in response to stress. FEBS Lett. 431, 319-321
50. 2-crystallin mRNA and protein in retina, brain, and testis. Investig. Ophthalmol. Vis. Sci. 14, 3056-3060
51. Crabb, J. W., Miyagi, M., Gu, X., Sharach, K., West, K. A., Sakaguchi, H., Kamei, M., Hasan, A., Yan, L., Raybom, M. E., Salomon, R. G., and Hollyfield, J. G. (2002) Drusen proteome analysis: an approach to the etiology of age-related macular degeneration. Proc. Natl. Acad. Sci. U. S. A. 995 14682-14687
52. Heidelberger, R., Wang, M. M., and Sherry, D. M. (2003) Differential distribution of synaptotagmin immunoreactivity among synapses in the goldfish, salamander, and mouse retina. Vis. Neurosci. 20, 37-49
53. Kovacs, B., and Gulya, K. (2003) Calmodulin gene expression in the neural retina of the adult rat. Life Sci. 73, 3213-3224
54. Fan, W., Agarwal, N., Kumar, M. D., and Cooper, N. G. (2005) Retinal ganglion cell death and neuroprotection: involvement of the CaMKIIα gene. Brain Res. Mol. Brain Res. 139, 306-316
55. Sharma, Y., and Balasubramanian, D. (1996) Calcium binding properties of β-crystallins. Ophthalmic Res. 28, 44-47