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Decomposition and long‐lasting downregulation of extracellular matrix in perineuronal nets induced by focal cerebral ischemia in rats
Author(s) -
Hobohm Carsten,
Günther Albrecht,
Grosche Jens,
Roßner Steffen,
Schneider Dietmar,
Brückner Gert
Publication year - 2005
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.20459
Subject(s) - perineuronal net , extracellular matrix , downregulation and upregulation , chondroitin sulfate proteoglycan , proteoglycan , microglia , thalamus , neuroscience , microbiology and biotechnology , chondroitin sulfate , pathology , immunostaining , immunocytochemistry , ischemia , extracellular , chemistry , glycosaminoglycan , biology , anatomy , medicine , biochemistry , immunology , immunohistochemistry , inflammation , gene
The upregulation of extracellular matrix components, especially chondroitin sulfate proteoglycans, after brain injury and stroke is known to accompany the glial reaction, forming repellent scars that hinder axonal growth and the reorganization of the injured neuronal networks. The extracellular matrix associated with perineuronal nets (PNs) in the primarily injured and remote regions has not yet been systematically analyzed. We use the model of permanent middle cerebral artery occlusion (MCAO) to investigate the acute and long‐lasting consequences of ischemia for PNs, related to the damage of neurons and reactions of glial cells, in spontaneously hypertensive rats. Extracellular matrix components associated with PNs around cortical interneurons and neurons in thalamic nuclei were characterized 1, 7, 14, and 35 days after MCAO, using Wisteria floribunda agglutinin (WFA) staining and immunocytochemistry. The degradation of PNs in the infarct core was initiated by loss of WFA‐binding matrix components, indicating the cleavage of glycosaminoglycan chains of chondroitin sulfate proteoglycans. Immunostaining showed the subsequent removal of proteoglycan core proteins within the extending microglia/macrophage invasion zone lasting for 2 weeks after MCAO. In the cortical periinfarct region, delineated by an astrocytic scar against the infarct core, the number of WFA‐stained and proteoglycan core protein‐immunoreactive PNs was permanently reduced. In the homolateral ventroposterior thalamus, the delayed decrease in perineuronal matrix was related to the distribution pattern of activated microglia and massive neuronal degeneration. It can be concluded from these results that complementary to the known upregulation of matrix components in the glial scar, deficits in the expression of the neuron‐associated extracellular matrix develop in the periinfarct and remote regions. These deficits may contribute to the long‐lasting functional impairments after stroke. © 2005 Wiley‐Liss, Inc.