Changes in the nucleolar and coiled body compartments precede lamina and chromatin reorganization during fibre cell denucleation in the bovine lens

European Journal of Cell Biology

Volumn 75, Issue 3, 1998, Pages 237-246

  Dahm, Ralf ^a   Gribbon, Christopher ^a   Quinlan, Roy A ^a   Prescott, Alan R ^a  

^a UNIVERSITY OF DUNDEE   (United Kingdom)

Author keywords

Apoptosis; Denucleation; Fibrillarin; Lamins; Lens; Transcription

Indexed keywords

ANIMAL CELL; APOPTOSIS; ARTICLE; CATARACT; CATTLE; CELL NUCLEUS; CELL ORGANELLE; CELL STRUCTURE; CHROMATIN CONDENSATION; LENS FIBER; LIGHT SCATTERING; NONHUMAN; NUCLEOLUS; PRIORITY JOURNAL;

EID: 0031924033     PISSN: 01719335     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0171-9335(98)80118-0     Document Type: Article

References (48)

1. Antoniou, M., M. Carmo-Fonseca, J. Ferreira, A. I. Lamond: Nuclear organization of splicing snRNPs during differentiation of murine erythroleukemia cells in vitro. J. Cell Biol. 123, 1055-1068 (1993).
2. Appleby, D. W., S. P. Modak: DNA degradation in terminally differentiating lens fiber cells from chick embryos. Proc. Natl. Acad. Sci. USA 74, 5579-5583 (1977).
3. Bassnett, S.: Mitochondrial dynamics in differentiating fiber cells of the mammalian lens. Curr. Eye Res. 11, 1227-1232 (1992).
4. Bassnett, S.: The fate of the Golgi apparatus and endoplasmic reticulum during lens fibre cell differentiation. Investig. Ophthalmol. Vis. Sci. 36, 1793-1803 (1995).
5. Bassnett, S.: Fiber cell denucleation in the primate lens. Investig. Ophthalmol. Vis. Sci. 38, 1678-1687 (1997).
6. Bassnett, S., D. C. Beebe: Coincident loss of mitochondria and nuclei during lens fibre cell differentiation. Dev. Dyn. 194, 85-93 (1992).
7. Bassnett, S., D. Malaic: Chromatin degradation in differentiating fiber cells of the eye lens. J. Cell Biol. 137, 37-49 (1997).
8. Bohmann, K., J. Ferreira, N. Santama, K. Weis, A. I. Lamond: Molecular analysis of the coiled body. J. Cell Sci. Suppl. 19, 107-113 (1995).
9. Capetanaki, Y., S. Smith, J. P. Heath: Overexpression of the vimentin gene in transgenic mice inhibits normal lens cell differentiation. J. Cell Biol. 109, 1653-1664 (1989).
10. Carmo-Fonseca, M., R. Pepperkok, M. T. Carvalho, A. I. Lamond: Transcription-dependent colocalization of the U1, U2, U4/U6, and U5 snRNPs in coiled bodies. J. Cell Biol. 117, 1-14 (1992).
11. Chaudun, E., C. Arruti, Y. Courtois, F. Ferrag, J. C. Jeanny, B. N. Patel, C. Skidmore, A. Torriglia, M. F. Counis: DNA strand breakage during physiological apoptosis of the embryonic chick lens-free 3′ OH end single-strand breaks do not accumulate even in the presence of a cation-independent deoxyribonuclease. J. Cell. Physiol. 158, 354-364 (1994).
12. Chow, R. L., G. D. Roux, M. Roghani, M. A. Palmer, D. B. Rifkin, D. A. Moscatelli, R. A. Lang: FGF suppresses apoptosis and induces differentiation of fiber cells in the mouse lens. Investig. Ophthalmol. Vis. Sci. 37, 5984 (1996).
13. Coates, P. J., D. Jamieson, K. Smart, A. R. Prescott, P. A. Hall: The prohibitin family of mitochondrial proteins regulates replicative lifespan. Curr. Biol. 7, 607-610 (1997).
14. Earnshaw, W.: Nuclear changes in apoptosis. Curr. Opin. Cell Biol. 7, 337-343 (1995).
15. Endresen, P. C., P. S. Prytz, J. Aarbakke: A net flow cytometric method for the discrimination of apoptotic cells and detection of their cell cycle specificity through staining of F-actin and DNA. Cytometry 20, 162-171 (1995).
16. Fromm, L., P. A. Overbeek: Inhibition of cell death by lens-specific Overexpression of bcl-2 in transgenic mice. Dev. Genet. 20, 276-287 (1997).
17. Harocopos, G. J., A. E. Kolker, D. C. Beebe: Is apoptosis associated with cataract formation in humans? Investig. Ophthalmol. Vis. Sci. 37, 5651 (1996).
18. Ishizaki, Y., J. T. Voyvodic, J. F. Burne, M. C. Raff: Control of lens epithelial cell survival. J. Cell Biol. 121, 899-908 (1993).
19. Khillan, J. S., M. K. Oskarsson, F. Propst, T. Kuwabara, G. F. Vande Woude, H. Westphal: Defects in lens fibre differentiation linked to c-mos overexpression in transgenic mice. Genes Dev. 1, 1327-1335 (1987).
20. Kuwabara, T.: The maturation of the lens cell: a morphologic study. Exp. Eye Res. 20, 427-443 (1975).
21. Kuwabara, T., M. Imaizumi: Denucleation process in the lens. Investig. Ophthalmol. Vis. Sci. 13, 973-981 (1974).
22. Lang, R. A.: Apoptosis in mammalian eye development: Lens morphogenesis, vascular regression and immune privilege. Cell Death and Differentiation 4, 12-20 (1997).
23. Lazebnik, Y. A., A. Takahashi, R. D. Moir, R. D. Goldman, G. G. Poirier, S. H. Kaufmann, W. C. Earnshaw: Studies of the lamin proteinase reveal multiple parallel biochemical pathways during apoptotic execution. Proc. Natl. Acad. Sci. USA 92, 9042-9046 (1995).
24. Li, W.-C., J. R. Kuszak, K. Dunn, R.-K. Wang, W. Ma, G.-M. Wang, A. Spector, M. Leib, A. M. Cotliar, M. Weiss, J. Espy, G. Howard, R. L. Farris, J. Auran, A. Donn, A. Hofelgt, C. Mackay, J. Merriam, R. Mittl, T. R. Smith: Lens epithelial cell apoptosis appears to be a common cellular basis for non-congenital cataract development in humans and animals. J. Cell Biol. 130, 169-181 (1995).
25. Liu, X. S., C. N. Kim, J. Yang, R. Jemmerson, X. D. Wang: Induction of apoptotic program in cell-free extracts - requirement for dATP and cytochrome c. Cell 86, 147-157 (1996).
26. Millar, A., A. Hooper, L. Copeland, F. Cummings, A. Prescott: Reorganisation of the microtubule cytoskeleton and centrosomal loss during lens fibre cell differentiation. Nova Acta Leopoldina 299, 169-183 (1997).
27. Modak, S. P., F. J. Bollum: Detection and measurement of single-strand breaks in nuclear DNA in fixed lens sections. Exp. Cell Res. 75, 307-313 (1972).
28. Morgenbesser, S. D., B. O. Williams, T. Jacks, R. A. Depinho: P53-dependent apoptosis produced by rb-deficiency in the developing mouse lens. Nature 371, 72-74 (1994).
29. Pan, H. C., A. E. Griep: Altered cell-cycle regulation in the lens of HPV-16 E6 or E7 transgenic mice - implications for tumor-suppressor gene-function in development. Genes Dev. 8, 1285-1299 (1994).
30. Piatigorsky, J.: Lens differentiation in vertebrates. A review of cellular and molecular features. Differentiation 19, 134-153 (1981).
31. Pugh, G., P. Coates, E. Lane, Y. Raymond, R. Quinlan: Distinct nuclear pathways for lamins A and C both lead to their increase during quiescence in Swiss 3T3 cells. J. Cell Sci. 110, 2483-2493 (1997).
32. Quinlan, R. A., J. M. Carter, A. Sandilands, A. R. Prescott: The beaded filament of the eye lens: an unexpected key to intermediate filament structure and function. Trends Cell Biol. 6, 123-126 (1996).
33. Rao, L., D. Perez, E. White: Lamin proteolysis facilitates nuclear events during apoptosis. J. Cell Biol. 135, 1441-1455 (1996).
34. Reimer, G., K. M. Pollard, C. A. Penning, R. L. Ochs, M. A. Lischwe, H. Busch, E. M. Tan: Monoclonal autoantibody from a (new-zealand black × new-zealand white) F1 mouse and some human scleroderma sera target an MR-34,000 nucleolar protein of the U3 RNP particle. Arthritis Rheum. 30, 793-800 (1987).
35. Robinson, M. L., L. A. Macmillancrow, J. A. Thompson, P. A. Overbeek: Expression of a truncated FGF receptor results in defective lens development in transgenic mice. Development 121, 3959-3967 (1995).
36. Sandilands, A., A. R. Prescott, J. M. Carter, A. M. Hutcheson, R. A. Quinlan, J. Richards, P. G. FitzGerald: Vimentin and CP49/Filensin form distinct networks in the lens which are independently modulated during lens fibre cell differentiation. J. Cell Sci. 108, 1397-1406 (1995).
37. Sandilands, A., A. R. Prescott, A. M. Hutcheson, R. A. Quinlan, J. T. Casselman, P. G. FitzGerald: Filensin is proteolytically processed during lens fiber cell differentiation by multiple independent pathways. Eur. J. Cell Biol. 67, 238-253 (1995).
38. Santama, N., C. G. Dotti, A. I. Lamond: Neuronal differentiation in the rat hippocampus involves a stage-specific reorganization of subnuclear structure both in vivo and in vitro. Eur. J. Neurosci. 8, 892-905 (1996).
39. Sanwal, M., A. Muel, E. Chaudun, Y. Courtois, M. Counis: Chromatin condensation and terminal differentiation process in embryonic chicken lens in vivo and in vitro. Exp. Cell Res. 167, 429-439 (1986).
40. Sax, C. M., J. Piatigorsky: Expression of the alpha-crystallin/small heat-shock protein/molecular chaperone genes in the lens and other tissues. Adv. Enzymol. Relat. Areas Mol. Biol. 69, 155-201 (1994).
41. Spector, D. L.: Macromolecular domains within the cell nucleus. Annu. Rev. Cell Biol. 9, 265-315 (1993).
42. Susin, S. A., N. Zamzami, M. Castedo, T. Hirsch, P. Marchetti, A. Macho, E. Daugas, M. Geuskens, G. Kroemer: Bcl-2 inhibits the mitochondrial release of an apoptogenic protcase. J. Exp. Med. 184, 1331-1341 (1996).
43. Uga, S., P. F. Kador, T. Kuwabara: Cytological study of Philly mouse cataract. Exp. Eye Res. 30, 79-92 (1980).
44. Van Engeland, M., H. J. H. Kuijpers, F. C. S. Ramaekers, C. P. M. Reutelingsperger, B. Schutte: Plasma membrane alterations and cytoskeletal changes in apoptosis. Exp. Cell Res. 235, 421-430 (1997).
45. Vrensen, G. F., J. Graw, A. De Wolf: Nuclear breakdown during terminal differentiation of primary lens fibres in mice: a transmission electron microscopic study. Exp. Eye Res. 52, 647-659 (1991).
46. Wride, M. A.: Cellular and molecular features of lens differentiation: A review of recent advances. Differentiation 61, 77-93 (1996).
47. Wyllie, A., J. Kerr, A.Currie: Cell death: the significance of apoptosis. Int. Rev. Cytol. 68, 251-305 (1980).
48. Zimmermann, L., R. Font: Congenital formation in the eye. Some recent advances in knowledge of the pathogenesis and histopathological characteristics. J. Am. Med. Assoc. 196, 684-692 (1966).