Cystatin C reduces the in vitro formation of soluble A beta 1-42 oligomers and protofibrils
(2007) In Scandinavian Journal of Clinical & Laboratory Investigation 67(2). p.179-190- Abstract
- There are an increasing number of genetic and neuropathological observations to suggest that cystatin C, an extracellular protein produced by all nucleated cells, might play a role in the pathophysiology of sporadic Alzheimer's disease (AD). Recent observations indicate that small and large soluble oligomers of the beta-amyloid protein (A beta) impair synaptic plasticity and induce neurotoxicity in AD. The objective of the present study was to investigate the influence of cystatin C on the production of such oligomers in vitro. Co-incubation of cystatin C with monomeric A beta 1-42 significantly attenuated the in vitro formation of A beta oligomers and protofibrils, as determined using electron microscopy (EM), dodecyl sulphate... (More)
- There are an increasing number of genetic and neuropathological observations to suggest that cystatin C, an extracellular protein produced by all nucleated cells, might play a role in the pathophysiology of sporadic Alzheimer's disease (AD). Recent observations indicate that small and large soluble oligomers of the beta-amyloid protein (A beta) impair synaptic plasticity and induce neurotoxicity in AD. The objective of the present study was to investigate the influence of cystatin C on the production of such oligomers in vitro. Co-incubation of cystatin C with monomeric A beta 1-42 significantly attenuated the in vitro formation of A beta oligomers and protofibrils, as determined using electron microscopy (EM), dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE), immunoblotting, thioflavin T (ThT) spectrofluorimetry and gel chromatography. However, cystatin C did not dissolve preformed A beta oligomers. Direct binding of cystatin C to A beta was demonstrated with the formation of an initial 1:1 molar high-affinity complex. These observations suggest that cystatin C might be a regulating element in the transformation of monomeric A beta to larger and perhaps more toxic molecular species in vivo. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/665304
- author
- Selenica, M. L. ; Wang, Xin LU ; Ostergaard-Pedersen, L. ; Westlind-Danielsson, A. and Grubb, Anders LU
- organization
- publishing date
- 2007
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- cysteine protease, beta amyloid protein, ADDLs, Alzheimer's disease, inhibitor
- in
- Scandinavian Journal of Clinical & Laboratory Investigation
- volume
- 67
- issue
- 2
- pages
- 179 - 190
- publisher
- Informa Healthcare
- external identifiers
-
- wos:000244842400008
- scopus:33947133671
- ISSN
- 1502-7686
- DOI
- 10.1080/00365510601009738
- language
- English
- LU publication?
- yes
- id
- 8386e901-ae22-4e7a-b2ec-ded7e80e5f7f (old id 665304)
- date added to LUP
- 2016-04-01 16:35:15
- date last changed
- 2023-01-05 00:49:21
@article{8386e901-ae22-4e7a-b2ec-ded7e80e5f7f, abstract = {{There are an increasing number of genetic and neuropathological observations to suggest that cystatin C, an extracellular protein produced by all nucleated cells, might play a role in the pathophysiology of sporadic Alzheimer's disease (AD). Recent observations indicate that small and large soluble oligomers of the beta-amyloid protein (A beta) impair synaptic plasticity and induce neurotoxicity in AD. The objective of the present study was to investigate the influence of cystatin C on the production of such oligomers in vitro. Co-incubation of cystatin C with monomeric A beta 1-42 significantly attenuated the in vitro formation of A beta oligomers and protofibrils, as determined using electron microscopy (EM), dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE), immunoblotting, thioflavin T (ThT) spectrofluorimetry and gel chromatography. However, cystatin C did not dissolve preformed A beta oligomers. Direct binding of cystatin C to A beta was demonstrated with the formation of an initial 1:1 molar high-affinity complex. These observations suggest that cystatin C might be a regulating element in the transformation of monomeric A beta to larger and perhaps more toxic molecular species in vivo.}}, author = {{Selenica, M. L. and Wang, Xin and Ostergaard-Pedersen, L. and Westlind-Danielsson, A. and Grubb, Anders}}, issn = {{1502-7686}}, keywords = {{cysteine protease; beta amyloid protein; ADDLs; Alzheimer's disease; inhibitor}}, language = {{eng}}, number = {{2}}, pages = {{179--190}}, publisher = {{Informa Healthcare}}, series = {{Scandinavian Journal of Clinical & Laboratory Investigation}}, title = {{Cystatin C reduces the in vitro formation of soluble A beta 1-42 oligomers and protofibrils}}, url = {{http://dx.doi.org/10.1080/00365510601009738}}, doi = {{10.1080/00365510601009738}}, volume = {{67}}, year = {{2007}}, }