Agrin is a major heparan sulfate proteoglycan accumulating in Alzheimer's disease brain

被引:116
作者
Verbeek, MM
Otte-Höller, I
van den Born, J
van den Heuvel, LPWJ
David, G
Wesseling, P
de Waal, RMW
机构
[1] Univ Nijmegen Hosp, Dept Pathol, Lab Pediat & Neurol 319, NL-6500 HB Nijmegen, Netherlands
[2] Univ Nijmegen Hosp, Dept Nephrol, NL-6500 HB Nijmegen, Netherlands
[3] Univ Nijmegen Hosp, Dept Pediat, NL-6500 HB Nijmegen, Netherlands
[4] Univ Nijmegen Hosp, Dept Neurol, NL-6500 HB Nijmegen, Netherlands
[5] Katholieke Univ Leuven, Ctr Human Genet, Louvain, Belgium
[6] Flanders Interuniv Inst Biotechnol, Louvain, Belgium
关键词
D O I
10.1016/S0002-9440(10)65529-0
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Heparan sulfate proteoglycans (HSPGs) have been suggested to play an important role in the formation and persistence of senile plaques and neurofibrillary tangles in dementia of the Alzheimer's type (DAT), We performed a comparative immunohistochemical analysis of the expression of the HSPGs agrin, perlecan, glypican-1, and syndecans 1-3 in the lesions of DAT brain neocortex and hippocampus. Using a panel of specific antibodies directed against the protein backbone of the various HSPG species and against the glycosaminoglycan (GAG) side-chains, we demonstrated the following. The basement membrane-associated HSPG, agrin, is widely expressed in senile plaques, neurofibrillary tangles and cerebral blood vessels, whereas the expression of the other basement membrane-associated HSPG, perlecan, is lacking in senile plaques and neurofibrillary tangles and is restricted to the cerebral vasculature. Glypican and three different syndecans, ail cell membrane-associated HSPG species, are also expressed in senile plaques and neurofibrillary tangles, albeit at a lower frequency than agrin, Heparan sulfate GAG side chains are also associated with both senile plaques and: neurofibrillary tangles. Our results suggest that glycosaminoglycan side chains of the HSPGs agrin, syndecan, and glypican, but not perlecan, may play an important role in the formation of both senile plaques and neurofibrillary tangles. In addition, we speculate that agrin, because it contains nine protease-inhibiting domains, may protect the protein aggregates in senile plaques and neurofibrillary tangles against extracellular proteolytic degradation, leading to the persistence of these deposits.
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页码:2115 / 2125
页数:11
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