The microglial response to progressive hydrocephalus in a model of inherited aqueductal stenosis

Neurological Research

Volumn 20, Issue 8, 1998, Pages 697-704

  Mangano, Francesco T ^a   McAllister, James P ^b,d   Jones, Hazel C ^c   Johnson, Martha J ^b,e   Kriebel, Richard M ^a  

^a PHILADELPHIA COLLEGE OF OSTEOPATHIC MEDICINE   (United States)

^b LERNER RESEARCH INSTITUTE   (United States)

^c UNIVERSITY OF FLORIDA HEALTH   (United States)

^d WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e NORTHWESTERN UNIVERSITY   (United States)

Author keywords

Aqueductal stenosis; Cerebral cortex; H Tx rat gliosis; Hydrocephalus; Inherited hydrocephalus; Microglia

Indexed keywords

AGE; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN AQUEDUCT STENOSIS; CELL STRUCTURE; CONTROLLED STUDY; DISEASE SEVERITY; GLIOSIS; GRAY MATTER; HISTOCHEMISTRY; HYDROCEPHALUS; MICROGLIA; NEWBORN; NONHUMAN; RAT; WHITE MATTER;

EID: 0031672710     PISSN: 01616412     EISSN: None     Source Type: Journal    
DOI: 10.1080/01616412.1998.11740586     Document Type: Article

References (46)

1. Russell DS. Observations on the pathology of hydrocephalus. Med Res Council Special Report Ser 1949; 265: 1-138
2. Blackburn BL, Fineman RM. Epidemiology of congenital hydrocephalus in Utah, 1940-1979: Report of an iatrogenically related 'epidemic'. Am J Med Genet 1994; 52: 123
3. Fernell E, Hagberg G, Hagberg B. Infantile hydrocephalus epidemiology: An indicator of enhanced survival. Arch Dis Child Fetal Neonatal Edn 1994; 70: 123-128
4. Williamson PA, Shauberger CW, Varner MW, Aschenbrener CA. Heterogeneity of prenatal onset hydrocephalus: Management and counseling implications. Am J Med Gen 1984; 17: 497-508
5. McAllister JP II, Chovan P. Neonatal hydrocephalus mechanism and consequences. Neurosurg CI N Am 1998; 9: 73-93
6. Fernell E, Hagberg G, Hagberg B. Infantile hydrocephalus - the impact of enhanced preterm survival. Acta Paediatr Scand 1990; 79: 1080-1086
7. Del Bigio MR, Da Silva MC, Drake JM, et al. Acute and chronic cerebral white matter damage in neonatal hydrocephalus. Can J Neurol Sci 1994; 21: 299
8. Del Bigio MR, Bruni JE. Periventricular pathology in hydrocephalic rabbits before and after shunting. Acta Neuropathol 1988; 77: 186
9. Takei F, Shapiro K, Hirano A, Kohn I. Influence of the rate of ventricular enlargement on the ultrastructural morphology of the white matter in experimental hydrocephalus. Neurosurgery 1987; 21: 645-650
10. Streit WJ, Kincaid-Colton CA. The brain's immune system. Scientific American 1995; Nov. 54-61
11. Davis EJ, Foster TD, Thomas WE. Cellular forms and functions of brain microglia. Brain Res Bull 1994; 34: 73-78
12. Ling EA. Brain macrophages in rats following intravenous labeling of mononuclear leukocytes with colloidal carbon. J Anat 1978; 125: 101-106
13. Spranger M, Fontana A. Activation of microglia: A dangerous interlude in immune function in the brain. Neuroscientist 1996; 2: 293-299
14. Amat JA, Hideaki I, Nakamura K, Norton WT. Phenotypic diversity and kinetics of proliferating microglia and astrocytes following cortical stab wounds. Glia 1996; 16: 386-392
15. Gehrmann J, Banati RB, Wiessnert C, Hossmann K-A, Kreutzberg GW. Reactive microglia in cerebral ischemia: An early mediator of tissue damage? [review]. Neuropath App Neurobiol 1995; 21: 277-289
16. McGeer PL, Kawamata T, Walker DG, Akiyama H, Tooyama I, McGeer EG. Microglia in degenerative neurological disease. Glia 1993; 7: 84-92
17. Watkins BA, Dorn HH, Kelly WB, Armstrong RC, Potts BJ, Michaels F, Kufta CV, Dubois-Dalcq M. Specific HIV-1 for microglial cells in primary human brain cultures. Science 1990; 249: 549-553
18. Buttini M, Limonta S, Boddeke HWGM. Peripheral administration of lipopolysaccharide induces activation of microglial cells in rat brain. Neurochem Int 1996; 29(1): 25-35
19. Jones C, Bucknall RM. Inherited prenatal hydrocephalus in the H-Tx rat: A morphological study. Neuropathol Appl Neurobiol 1988; 14: 263-274
20. Kruger L, Saporta S, Swanson LW. Photographic atlas of the rat brain. The Cell and Fiber Architecture Illustrated in Three Planes with Stereotaxic Coordinates, New York: Cambridge University Press, 1995
21. del Rio Hortega P. Microglia. In: Penfield W, ed. Cytology and Cellular Pathology of the Nervous System, New York: Hoeber PB, 1932: pp. 481-534
22. Streit WJ, Kreutzberg GW. Lectin binding by resting and reactive microglia. J Neurocytol 1987; 16: 249-260
23. Liener IE, Sharon N, Goldstein IJ. The Lectins. Properties, Functions, and Applications in Biology and Medicine, Orlando: Academic Press Inc, 1986
24. Hayes CE, Goldstein IJ. An α-D-galactosyl-binding lectin from Bandeiraea simplicifolia seeds. J Biol Chem 1974; 249: 1904-1914
25. Fix AS, Ross JF, Stitzel SR, Switzer RC. Integrated evaluation of central nervous system lesions: Stains for neurons, astrocytes, and microglia reveal the spatial and temporal features of MK-801-induced neuronal necrosis in the rat cerebral cortex. Toxicologic Pathology 1996; 24: 291-304
26. Ohshige-Hayashi Y, Kiyama H. Expression of Glycine max (soybean agglutinin) binding molecule in injured motoneurons and its specific localization in the extracellular matrix between injured neurons and microglia. Neurosci Res 1997; 27: 271-275
27. Streit WJ, Sparks L. Activation of microglia in the brains of humans with heart disease and hypercholesterolemic rabbits. J Mol Med 1997; 75: 130-138
28. Wu CH, Chien HF, Chang CY, Ling EA. Heterogeneity of antigen expression and lectin labeling on microglial cells in the olfactory bulb of adult rats. Neurosci Res 1997; 28: 67-75
29. Zhang Z, Chopp M, Powers C. Temporal profile of microglial response following transient (2 h) middle cerebral artery occlusion. Brain Res 1997; 744: 189-198
30. Harris NG, Jones HC, Patel S. Ventricle shunting in young H-Tx rats with inherited congenital hydrocephalus: A quantitative histological study of cortical gray matter. Child's Nerv Syst 1994; 10: 1-6
31. Nishiyama A, Yu M, Drazba JA, Tuohy VK. Normal and reactive NG2 + glial cells are distinct from resting and activated microglia. J Neurosci Res 1997; 48: 299-312
32. Jones HC, Bucknall RM, Harris NG. The cerebral cortex in congenital hydrocephalus in the H-Tx rat: A quantitative light microscopy study. Acta Neuropathol 1991; 82: 217-224
33. Engel S, Wehner HD, Meyerman R. Expression of microglial markers in the human CNS after closed head injury. Acta Neurochir 1996; 66 (Suppl.): 87-95
34. Seeger G, Härtig W, Robner S, Schliebs R, Brückner G, Bigl V, Brauer K. Electron microscopic evidence for microglial phagocytic activity and cholinergic cell death after administration of the immunotoxin 1921gC-Saporin in rat. J Neurosci Res 1997; 48: 465-476
35. Streit WJ, Graeber MB, Kreutzberg GW. Functional plasticity of microglia: A review. Glia 1988; 1: 301-307
36. Giulian D, Baker TJ, Shih L-CN, Lachman LB. Interleukin-1 of the central nervous system is produced by ameboid microglia. J Exp Med1986; 164: 594-604
37. Giulian D, Lachman LB. Interleukin-1 stimulation of astroglial proliferation after brain injury. Science 1985; 228: 497-499
38. Kreutzberg GW. Microglia: A sensor for pathological events in the CNS. Trends Neurosci 1996; 19: 312-318
39. Ivacko JA, Sun R, Silverstein FS. Hypoxic-ischemic brain injury induces an acute microglial reaction in perinatal rats. Pediatric Res 1996; 39: 39-47
40. Medana IM, Hunt NH, Chan-Ling T. Early activation of microglia in the pathogenesis of fatal murine cerebral malaria. Glia 1997; 19: 91-103
41. Wu CH, Wang HJ, Wen CY, Lien KC, Ling EA. Response of amoeboid and ramified microglial cells to lipopolysaccharide injections in postnatal rats - a lectin and ultrastructural study. Neurosci Res 1997; 27: 133-141
42. Lu J, Kaur C, Ling EA. An immunohistochemical study of the intraventricular macrophages in induced hydrocephalus in prenatal rats following a maternal injection of 6-aminonicotinamide. J Anat 1996; 188: 491-495
43. Miwa S, Inagaki C, Fujiwara M, Takaori S. The activities of noradrenergic and dopaminergic neuron systems in experimental hydrocephalus. J Neurosurg 1982; 57: 67-73
44. Suda K, Sato K, Takeda N, Wada M, Miyazawa T, Arai H, Ito M, Miyaoka M. Early vs delayed ventriculoperitoneal shunt-effects on the impairment of the developing brain in congenitally hydrocephalic H-Tx rats. In: Matsumoto S, Tamaki N, eds. Hydrocephalus. Pathogenesis and Treatment, Tokyo: Springer-Verlag, 1991: pp. 10-26
45. Way JS, Katz SD, McAllister JP II. Effects of experimental infantile hydrocephalus and ventriculoperitoneal shunts on connections of the motor cortex. Soc Neurosci Abstr 1990; 16: 846
46. Longatti PL, Guida F, Agostini S, Camiato B, Carteri A. The CSF myelin basic protein in pediatric hydrocephalus. Child's Nervous System 1994; 10: 96-98