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Title: Small heat shock proteins associated with cerebral amyloid angiopathy of hereditary cerebral hemorrhage with amyloidosis (Dutch type) induce interleukin-6 secretion.
Author(s): Wilhelmus, M.M. (298979276)
Boelens, W.C. (107821575)
Kox, M. (313070989)
Maat-Schieman, M.L.
Veerhuis, R.
Waal, R.M.W. de (068460163)
Verbeek, M.M. (15230147X)
Publication year: 2009
Document type: Article / Letter to editor
Journal: Neurobiology of Aging
ISSN: 0197-4580
Volume: vol. 30
Issue: iss. 2
Start page: p. 229
End page: p. 240
Abstract: In hereditary cerebral hemorrhage with amyloidosis of the Dutch type (HCHWA-D), severe cerebral amyloid angiopathy (CAA) is associated with an inflammatory reaction. Small heat shock proteins (sHsps) are molecular chaperones and association of HspB8 with CAA in HCHWA-D has been observed. The aims of this study were to investigate (1) if other sHsps are associated with the pathological lesions in HCHWA-D brains, (2) if the amyloid-beta protein (A beta) increases production of sHsps in cultured cerebral cells and (3) if sHsps are involved in the cerebral inflammatory processes in both Alzheimer's disease (AD) and HCHWA-D. We conclude that Hsp20, HspB8 and HspB2 are present in CAA in HCHWA-D, and that A beta did not affect cellular sHsps expression in cultured human brain pericytes and astrocytes. In addition, we demonstrated that Hsp20, HspB2 and HspB8 induced interleukin-6 production in cultured pericytes and astrocytes, which could be antagonized by dexamethasone, whereas other sHsps and A beta were inactive, suggesting that sHsps may be among the key mediators of the local inflammatory response associated with HCHWA-D and AD lesions.
Subject: DCN 1: Perception and Action
DCN 2: Functional Neurogenomics
NCEBP 11: Alzheimer Centre
Organization: Neurology
Laboratory of Genetic, Endocrine and Metabolic Diseases
Intensive Care
Biomolecular Chemistry
Pathology
UMCN Extern
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/81507

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