Perineuronal nets potentially protect against oxidative stress

Experimental Neurology

Volumn 188, Issue 2, 2004, Pages 309-315

  Morawski, Markus ^a   Brückner, Martina K ^a   Riederer, Peter ^b   Brückner, Gert ^a   Arendt, Thomas ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

^b UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

Alzheimer's disease; Human cerebral cortex; Lipofuscin; Oxidative stress; Perineuronal net

Indexed keywords

GLYCOSAMINOGLYCAN; HYALURONIC ACID; LIPID; LIPOFUSCIN; PROTEOCHONDROITIN SULFATE; TENASCIN;

ADULT; AGED; ALZHEIMER DISEASE; ARTICLE; BRAIN CORTEX; CATALYSIS; CELL SUBPOPULATION; CONTROLLED STUDY; EXTRACELLULAR MATRIX; FEMALE; HOMEOSTASIS; HUMAN; HUMAN CELL; HUMAN TISSUE; LYSOSOME; MALE; MICROENVIRONMENT; NERVE CELL; NERVE DEGENERATION; NERVE SHEATH; NEUROPROTECTION; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN CROSS LINKING;

AGED; AGED, 80 AND OVER; ALZHEIMER DISEASE; CELL COUNT; CEREBRAL CORTEX; EXTRACELLULAR MATRIX; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; LIPOFUSCIN; MALE; MIDDLE AGED; NEURONS; OXIDATIVE STRESS; PYRAMIDAL CELLS;

EID: 3042830849     PISSN: 00144886     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.expneurol.2004.04.017     Document Type: Article

References (50)

1. Adams I., Brauer K., Arelin C., Härtig W., Fine A., Mader M., Arendt T., Brückner G. Perineuronal nets in the rhesus monkey and human basal forebrain including basal ganglia. Neuroscience. 108:2001;285-298
2. Arendt T. Alzheimer's disease a disorder of mechanism underlying structural brain self-organization. Neuroscience. 102:2001;723-765
3. Berardi N., Pizzorusso T., Ratto G.M., Maffei L. Molecular basis of plasticity in the visual cortex. Trends Neurosci. 26:2003;369-378
4. Bergeron C., Petrunka C., Weyer L. Copper/zinc superoxide dismutase expression in the human central nervous system. Correlation with selective neuronal vulnerability. Am. J. Pathol. 148:1996;273-279
5. Bertolotto A., Rocca G., Canavese G., Migheli A., Schiffer D. Chondroitin sulfate proteoglycan surrounds a subset of human and rat CNS neurons. J. Neurosci. Res. 29:1991;225-234
6. Boellaard J.W., Schlote W. Ultrastructural heterogeneity of neuronal lipofuscin in the normal human cerebral cortex. Acta Neuropathol. (Berl). 71:1986;285-294
7. Braak H., Braak E. Neuropathological staging of Alzheimer-related changes. Acta Neuropathol. (Berl). 82:1991;239-259
8. Braak H., Del Tredici K., Schultz C., Braak E. Vulnerability of select neuronal types to Alzheimer's disease. Ann. N. Y. Acad. Sci. 924:2000;53-61
9. Brodmann K. Vergleichende Lokalisationslehre der Großhirnrinde. 1909;Barth, Leipzig
10. Brunk U.T., Terman A. Lipofuscin: mechanisms of age-related accumulation and influence on cell function. Free Radic. Biol. Med. 33:2002;611-619
11. Brückner G., Brauer K., Härtig W., Wolff J.R., Rickmann M.J., Derouiche A., Delpech B., Girard N., Oertel W.H., Reichenbach A. Perineuronal nets provide a polyanionic, glia-associated form of microenvironment around certain neurons in many parts of the rat brain. Glia. 8:1993;183-200
12. Brückner G., Härtig W., Kacza J., Seeger J., Welt K., Brauer K. Extracellular matrix organization in various regions of rat brain grey matter. J. Neurocytol. 25:1996;333-346
13. Brückner G., Bringmann A., Härtig W., Köppe G., Delpech B., Brauer K. Acute and long-lasting changes in extracellular-matrix chondroitin-sulphate proteoglycans induced by injection of chondroitinase ABC in the adult rat brain. Exp. Brain Res. 121:1998;300-310
14. Brückner G., Hausen D., Härtig W., Drlicek M., Arendt T., Brauer K. Cortical areas abundant in extracellular matrix chondroitin sulphate proteoglycans are less affected by cytoskeletal changes in Alzheimer's disease. Neuroscience. 92:1999;791-805
15. Brückner G., Grosche J., Hartlage-Rübsamen M., Schmidt S., Schachner M. Region and lamina-specific distribution of extracellular matrix proteoglycans, hyaluronan and tenascin-R in the mouse hippocampal formation. J. Chem. Neuroanat. 26:2003;37-50
16. Celio M.R., Blümcke I. Perineuronal nets - A specialized form of extracellular matrix in the adult nervous system. Brain Res. Rev. 19:1994;128-145
17. Celio M.R., Spreafico R., De Biasi S., Vitellaro-Zuccarello L. Perineuronal nets: past and present. Trends Neurosci. 21:1998;510-515
18. Coyle J.T., Puttfarcken P. Oxidative stress, glutamate, and neurodegenerative disorders. Science. 262:1993;689-695
19. Crichton R.R., Wilmet S., Legssyer R., Ward R.J. Molecular and cellular mechanisms of iron homeostasis and toxicity in mammalian cells. J. Inorg. Biochem. 91:2002;9-18
20. Dityatev A., Schachner M. Extracellular matrix molecules and synaptic plasticity. Nat. Rev. Neurosci. 4:2003;456-468
21. Golgi C. Intorno all' origine del quarto nervo cerebrale e una questione isto-fisiologica che a questo argomento si collega. Rend. R. Accad. Lincei. 2:1893;379-389
22. Härtig W., Derouiche A., Welt K., Brauer K., Grosche J., Mader M., Reichenbach A., Brückner G. Cortical neurons immunoreactive for the potassium channel Kv3.1b subunit are predominantly surrounded by perineuronal nets presumed as a buffering system for cations. Brain Res. 842:1999;15-29
23. Hausen D., Brückner G., Drlicek M., Härtig W., Brauer K., Bigl V. Pyramidal cells ensheathed by perineuronal nets in human motor and somatosensory cortex. NeuroReport. 7:1996;1725-1729
24. Hirai K., Aliev G., Nunomura A., Fujioka H., Russell R.L., Atwood C.S., Johnson A.B., Kress Y., Vinters H.V., Tabaton M., Shimohama S., Cash A.D., Siedlak S.L., Harris P.L., Jones P.K., Petersen R.B., Perry G., Smith M.A. Mitochondrial abnormalities in Alzheimer's disease. J. Neurosci. 1(21):2001;3017-3023
25. Hirsch E.C. Why are nigral catecholaminergic neurons more vulnerable than other cells in Parkinson's disease? Ann. Neurol. 32:1992;88-93. (Supplement)
26. Hockfield S., Kalb R.G., Zaremba S., Fryer H. Expression of neural proteoglycans correlates with the acquisition of mature neuronal properties in the mammalian brain. Cold Spring Harbor Symp. Quant. Biol. 55:1990;505-514
27. Hof P.R., Giannakopoulos P., Vickers J.C., Bouras C., Morrison J.H. The morphologic and neurochemical basis of dementia: aging, hierarchical patterns of lesion distribution and vulnerable neuronal phenotype. Rev. Neurosci. 6:1995;97-124
28. Joseph J.A., Fisher D.R., Strain J. Muscarinic receptor subtype determines vulnerability to oxidative stress in COS-7 cells. Free Radic. Biol. Med. 32:2002;153-161
29. Köppe G., Brückner G., Härtig W., Delpech B., Bigl V. Characterization of proteoglycan-containing perineuronal nets by enzymatic treatments of rat brain sections. Histochem. J. 29:1997;11-20
30. Mann D.M., Yates P.O., Marcyniuk B. Relationship between pigment accumulation and age in Alzheimer's disease and Down syndrome. Acta Neuropathol. (Berl). 63:1984;72-77
31. Matthews R.T., Kelly G.M., Zerillo C.A., Gray G., Tiemeyer M., Hockfield S. Aggrecan glycoforms contribute to the molecular heterogeneity of perineuronal nets. J. Neurosci. 22:2002;7536-7547
32. McKhann G., Drachmann D., Folstein M., Katzmann R., Price D., Stadlan E.M. Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA workgroup under the auspices of Department of Health and Human Service Task Force on Alzheimer's disease. Neurology. 34:1984;939-944
33. Morrison J.H., Hof P.R. Life and death of neurons in the aging brain. Science. 278:1997;412-419
34. Moosmann B., Behl C. Cytoprotective antioxidant function of tyrosine and tryptophan residues in transmembrane proteins. Eur. J. Biochem. 267:2000;5687-5692
35. Newell K.L., Hyman B.T., Growdon J.H., Hedley-Whyte E.T. Application of the National Institute on Aging (NIA)-Reagan Institute criteria for the neuropathological diagnosis of Alzheimer disease. J. Neuropathol. Exp. Neurol. 58:1999;1147-1155. (November)
36. Ojima H., Sakai M., Ohyama J. Molecular heterogeneity of Vicia villosa-recognized perineuronal nets surrounding pyramidal and nonpyramidal neurons in the guinea pig cerebral cortex. Brain Res. 786:1998;274-280
37. Oohira A., Katoh-Semba R., Watanabe E., Matsui F. Brain development and multiple molecular species of proteoglycan. Neurosci. Res. 20:1994;195-207
38. Pizzorusso T., Medini P., Berardi N., Chierzi S., Fawcett J.W., Maffei L. Reactivation of ocular dominance plasticity in the adult visual cortex. Science. 298:2002;1248-1251
39. Porta E.A. Pigments in aging: an overview. Ann. N. Y. Acad. Sci. 959:2002;57-65
40. Ramón Y Cajal S. Las células de cilindro-eje corto de la capa molecular del cerebro. Rev. Trimest. Microgr. 1987
41. Reinert T., Morawski M., Arendt T., Butz T. Quantitative microanalysis of perineuronal nets in brain tissue. Nucl. Instrum. Methods B. 210:2003;395-400
42. Rhodes K.E., Fawcett J.W. Chondroitin sulphate proteoglycans: preventing plasticity or protecting the CNS? J. Anat. 204:2004;33-48
43. Seeger G., Brauer K., Härtig W., Brückner G. Mapping of perineuronal nets in the rat brain stained by colloidal iron hydroxide histochemistry and lectin cytochemistry. Neuroscience. 58:1994;371-388
44. Sohal R.S., Brunk U.T. Lipofuscin as an indicator of oxidative stress and aging. Adv. Exp. Med. Biol. 266:1989;17-26. (discussion 27-9)
45. Stojanovic A., Roher A.E., Ball M.J. Quantitative analysis of lipofuscin and neurofibrillary tangles in the hippocampal neurons of Alzheimer disease brains. Dementia. 5:1994;229-233
46. Sumpter P.Q., Mann D.M., Davies C.A., Yates P.O., Snowden J.S., Neary D. An ultrastructural analysis of the effects of accumulation of neurofibrillary tangle in pyramidal neurons of the cerebral cortex in Alzheimer's disease. Neuropathol. Appl. Neurobiol. 12:1986;305-319
47. Tappel A.L. Lipid peroxidation damage to cell components. Fed. Proc. 32:1973;1870-1874
48. The National Institute on Aging and Reagan Institute Working Group on Diagnostic Criteria for the Neuropathological Assessment of Alzheimer's Disease Consensus recommendations for the postmortem diagnosis of Alzheimer's disease. Neurobiol. Aging. 18:1997;1-2
49. A receptor α1 subunit from a unique entity in rat cerebral cortex. Exp. Neurol. 184:2003;705-714
50. Yamaguchi Y. Lecticans: organizers of the brain extracellular matrix. Cell. Mol. Life Sci. 57:2000;276-289