Intermediate filament change in astrocytes following mild cortical contusion

GLIA

Volumn 16, Issue 3, 1996, Pages 266-275

  Baldwin, Stanley A ^a   Scheff, Stephen W ^a  

^a UNIVERSITY OF KENTUCKY   (United States)

Author keywords

Glial fibrillary acidic protein; Proliferation; Vimentin

Indexed keywords

EID: 0030106237     PISSN: 08941491     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1098-1136(199603)16:3<266::aid-glia9>3.0.co;2-%23     Document Type: Article

References (54)

1. Aghajanian, A. and Bloom, F. (1967) The formation of synaptic junctions in developing rat brain: A quantitative electron microscopic study. Brain Res., 6:716-727.
2. Barres, B. (1991) New roles of glia. J. Neurosci., 11:3685-3694.
3. Blue, M. and Parnavelas, J. (1983) The formation and maturation of synapses in the visual cortex of the rat. II. Quantitative analysis J. Neurocytol., 12:697-712.
4. Brand, S. and Rakic, P. (1984) Cytodifferentiation and synaptogenesis in the neostriatum of fetal and neonatal rhesus monkeys. Anat. Embryol., 169:21-34.
5. Caley, D. and Maxwell, D. (1968) An electron microscopic study of the neuroglia during postnatal development of the rat cerebellum. J. Comp. Neurol., 113:45-70.
6. Ciesielski-Treska, J., Bader, M., and Aunis, D. (1982a) Microtubular organization in flat epitheloid and stellate process-bearing astrocytes in culture. Neurochem. Res., 7:275-286.
7. Ciesielski-Treska, J., Guerold, B., and Aunis, D. (1982b) Immunofluorescence study on the organization of actin in astroglial cells in primary cultures. Neuroscience, 7:502-522.
8. Cortez, S., McIntosh, T., and Noble, L. (1982) Experimental fluid percussion brain injury: Vascular disruption and neuronal and glial alterations. Brain Res., 482:271-282.
9. Cotman, C. and Nadler, V. (1978) Reactive synaptogenesis in the hippocampus. In: Neuronal Plasticity. C. Cotman, ed. Raven Press, New York, pp 227-271.
10. Dixon, C., Lyeth, B., Povlishock, J., Findling, R., Hamm, R., Marmarou, A., Young, H., and Hayes, R. (1987) A fluid percussion model of experimental brain injury in the rat: Neurological physiological and histopathological characterization. J. Neurosurg., 67:110-119.
11. Dixon, C., Lighthall, J., and Anderson, T. (1988) Physiologic, histopathologic, and cineradiographic characterization of a new fluid-percussion model of experimental brain injury in the rat. J. Neurotrauma, 5:91-104.
12. Dixon, C., Clifton, G , Lighthall, J., Yaghmai, A., and Hayes, R. (1991) A controlled cortical impact model of traumatic brain injury in the rat. J. Neurosci. Methods, 39:253-262.
13. Duffy, P. (1983) Astrocytes: Normal, Reactive and Neoplastic. Raven Press, New York.
14. Dyson, S. and Jones, D. (1976) Some effects of undernutrition on synaptic development: A quantitative ultrastructural study. Brain Res., 114:365-378.
15. Edelman, G. (1985) Cell adhesion and the molecular process of morphogenesis. Annu. Rev. Biochem., 54:135-169.
16. Fagan, A. and Gage, F. (1990) Cholinergic sprouting in the hippocampus: A proposed role for IL-1. Exp. Neurol., 110:105-120.
17. Fedoroff, S. (1985) Macroglial cell lineages. In: Molecular Bases of Neural Development. W. Edelman, W. Gall, and W. Cowan, eds. Raven Press, New York, pp. 91-117
18. Gage, F., Olejniczak, P., and Armstrong, D. (1988) Astrocytes are important for sprouting in the septohippocampal circuit. Exp. Neurol., 102:2-13.
19. Gilmore, S., Sims, T., and Leiting, J (1990) Astrocytic reaction in spinal gray matter following sciatic axotomy. Glia, 3:342-349.
20. Glezer, I. and Morgane, P. (1990) Ultrastructure of synapses and Golgi analysis of neurons in neocortex of the lateral gyrus (visual cortex) of the dolphin and pilot whale. Brain Res. Bull., 24:401-427.
21. Gomi, H., Yokoyama, T., Fujimoto, K., Ikeda, T., Katoh, A., Itoh, T., and Itohara, S. (1995) Mice devoid of the glial fibrillary acidic protein develop normally and are susceptible to scrapie prions. Neuron, 14:29-41.
22. Hayes, R., Stalhammer, D., Povlishock, J., Allen, A., Galinat, B., Becker, D., and Stonnington, H. (1987) A new model of concussive brain injury in the cat produced by extradural fluid volume loading. I. Physiological and neuropathological observations. Brain Injury, 1:93-112.
23. Hozumi, I., Chiu, F., and Norton, W. (1990) Biochemical and immunocytochemical changes in glial fibrillary acidic protein after stab wounds. Brain Res., 524:64-71.
24. Kempski, O. and Volk, C. (1994) Neuron-glial interaction during injury and edema of the CNS. Acta Neurochir., 60:7-11.
25. Langan, T. and Slater, M. (1992) Astrocytes derived from long-term primary cultures recapitulate features of astrogliosis as they reenter the cell division cycle. Brain Res., 577.200-209.
26. Lighthall, J., Goshgarian, H., and Pinderski, C. (1990) Characterization of axonal injury produced by controlled cortical impact. J. Neurotrauma, 7:65-76.
27. Lindren, S. and Rinder, L. (1966) Experimental studies in head injury. II. Pressure propagation in "percussive concussion". Biophysik, 3:174-180.
28. Malhotra, S., Shnitka, T., and Elbrink, J. (1990) Reactive astrocytes - a review. Cytobios, 61:133-160.
29. Mathewson, A. and Berry, M. (1985) Observation on the astrocyte response to a cerebral stab wound in adult rats. Brain Res., 327.61-69.
30. Mikucki, S. and Oblinger, M. (1991) Vimentin mRNA expression increases after corticospinal axotomy in the adult hamster. Metab. Brain Dis., 6:33-49.
31. Miyake, T., Hattori, T., Fukuda, M., Kitamura, T., and Fujita, S. (1988) Quantitative studies on proliferative changes of reactive astrocytes in mouse cerebral cortex. Brain Res., 451:133-138.
32. Oblinger, M. and Singh, L. (1993) Reactive astrocytes in neonate brain upregulate intermediate filament gene expression in response to axonal injury. Int. J. Dev. Neurosci., 11:149-156.
33. Oppenheim, R., Chu-Wang, I., and Foelix, R. (1975) Some aspects of synaptogenesis in the spinal cord of the chick embryo: A quantitative electron microscopic study. J. Comp. Neurol., 161:383-418.
34. Palay, S., McGee-Russell, S., Spencer, G., and Grillo, M. (1962) Fixation of neural tissues for electron microscopy by perfusion with solutions of osmium tetraoxide. J. Cell Biol., 12:385-410.
35. Petito, C., Morgello, S., Felix, J., and Lesser, M. (1990) The two patterns of reactive astrocytosis in postischemic rat brain. J. Cereb. Blood Flow Metab., 10:850-859.
36. Petito, C., Chung, M., Halaby, I , and Cooper, A. (1992) Influence of the neuronal environment on the pattern of reactive astrocytosis following cerebral ischemia. Prog. Brain Res., 94:381-387.
37. Pixley, S. and de Vellis, J. (1984) Transition between immature radial glia and mature astrocytes studied with a monoclonal antibody to vimentin. Dev. Brain Res., 15:201-209.
38. Poirier, J., Hess, M., May, P., and Finch, C. (1991) Astrocytic apolipoprotein E mRNA and GFAP mRNA in hippocampus after entorhinal cortex lesioning. Mol. Brain Res., 11:97-106.
39. Privat, A. and Rataboul, P. (1988) Fibrous and protoplasmic astrocytes. In: Astrocytes: Cell Biology and Pathology of Astrocytes S. Fedoroff and A. Vernadakis, eds. Academic Press, New York, pp. 105-129.
40. Raisman, G (1985) Synapse formation in the septal nuclei of adult rats. In: Synaptic Plasticity C. Cotman, ed. Guilford Press, New York, pp. 13-37.
41. Scheff, S. (1989) Synaptic reorganization after injury: The hippocampus as a model system. In: Neural Regeneration and Transplantation. F.J. Seil, ed. Alan R. Liss, New York, pp. 137-156.
42. Schiffer, D., Giordana, T., Mighelgi, A., Giaccone, G., Pezzotta, S., and Mauro, A. (1986) Glial fibrillary acidic protein and vimentin in the experimental glial reaction of the rat brain. Brain Res., 374:110-118.
43. Schiffer, D., Giordana, M., Cavalla, P., Vigliani, M., and Attanasio, A. (1993) Immunohistochemistry of glial reaction after injury in the rat: Double stainings and markers of cell proliferation. Int. J. Dev. Neurosci., 11:269-280.
44. Shao, Y., Enkvist, K., and McCarthy, K. (1994) Glutamate blocks astroglial stellation: Effect of glutamate uptake and volume changes. Glia, 11:1-10.
45. Singh, D. and Mathew, T. (1989) Immunocytochemical studies of astrocytes following injury to the cerebral cortex of the rat. Acta Anat., 134:156-159.
46. Steward, O., Cotman, C., and Lynch, G. (1974) Growth of a new fiber projection in the brain of adult rats: Re-innervation of the dentate gyrus by the contralateral entorhinal cortex following ipsilateral entorhinal lesions. Exp. Brain Res., 20:45-66
47. Steward, O., Torre, E , Phillips, L., and Trimmer, P. (1990) The process of reinnervation in the dentate gyrus of adult rats: Time course of increase in mRNA for glial fibrillary acidic protein. J. Neurosci., 10:2373-2384.
48. Stichel, C. and Muller, H. (1994) Extensive and long-lasting changes of glial cells following transection of the postcommissural fornix in the adult rat. Glia, 10:89-100.
49. Suzuki, M. and Choi, B. (1991) Repair and reconstruction of the cortical plate following closed cryogenic injury to the neonatal rat cerebrum. Acta Neuropathol., 82:93-101.
50. Takahashi, T., Nowakowski, R., and Caviness, V. (1992) BrdU as an S-phase marker for quantitative studies of cytokinetic behaviour in the murine cerebral ventricular zone. J. Neurocytol., 21:185-197.
51. Takamiya, Y., Kohsaka, S., Toya, S., Otani, M., and Tsukada, Y. (1988) Immunohistochemical studies on the proliferation of reactive astrocytes and the expression of cytoskeletal proteins following brain injury in rats. Dev. Brain Res., 38:201-210.
52. Tetzlaff, W., Graeber, M., Bisby, M., and Kreutzberg, G. (1988) Increased glial fibrillary acidic protein synthesis in astrocytes during retrograde reaction of the rat facial nucleus. Glia, 1:90-95.
53. Weinstein, D., Shelanski, M., and Liem, R. (1991) Suppression by antisense mRNA demonstrates a requirement for the glial fibrillary acidic protein in the formation of stable astrocytic process in response to neurons. J. Cell Biol., 112:1205-1213.
54. Wenzel, J., Lammert, G., Meyer, U., and Krug, M. (1991) The influence of long-term potentiation on the spatial relationship between astrocyte processes and potentiated synapses in the dentate gyrus neuropil of rat brain. Brain Res., 560:122-131.