Amyloid aggregation and deposition of human islet amyloid polypeptide at membrane interfaces. (30th April 2014)
- Record Type:
- Journal Article
- Title:
- Amyloid aggregation and deposition of human islet amyloid polypeptide at membrane interfaces. (30th April 2014)
- Main Title:
- Amyloid aggregation and deposition of human islet amyloid polypeptide at membrane interfaces
- Authors:
- Sasahara, Kenji
Morigaki, Kenichi
Shinya, Kyoko - Abstract:
- <abstract abstract-type="main" id="febs12807-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Amyloid deposition of human islet amyloid polypeptide (hIAPP) within the islets of Langerhans is a pathological feature of type 2 diabetes mellitus. Substantial evidence indicates that the membrane‐mediated aggregation and subsequent deposition of hIAPP are linked to dysfunction and death of pancreatic β‐cells, but the molecular processes of hIAPP deposition are poorly understood. In this study, we examined the membrane‐mediated aggregation and deposition of hIAPP at supported planar lipid bilayers with and without raft components (i.e. cholesterol and sphingomyelin) to provide insight into hIAPP‐induced membrane dysfunction. The adsorption of hIAPP onto the bilayers was studied using a quartz crystal microbalance with dissipation monitoring, which showed enhanced accumulation of the peptide onto the bilayer containing raft components. Microscope observations demonstrated the growth of the aggregates formed from the membrane‐adsorbed hIAPP. The examination of the membrane interfaces revealed that hIAPP aggregates retained the ability to associate with the membranes during the aggregation process, resulting in insertion of the aggregates into the bilayers. We also report the inhibitory effect of insulin on the hIAPP deposition. These findings demonstrate the aggregation of hIAPP at the membrane interfaces leading to amyloid deposits associated with the membrane and<abstract abstract-type="main" id="febs12807-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Amyloid deposition of human islet amyloid polypeptide (hIAPP) within the islets of Langerhans is a pathological feature of type 2 diabetes mellitus. Substantial evidence indicates that the membrane‐mediated aggregation and subsequent deposition of hIAPP are linked to dysfunction and death of pancreatic β‐cells, but the molecular processes of hIAPP deposition are poorly understood. In this study, we examined the membrane‐mediated aggregation and deposition of hIAPP at supported planar lipid bilayers with and without raft components (i.e. cholesterol and sphingomyelin) to provide insight into hIAPP‐induced membrane dysfunction. The adsorption of hIAPP onto the bilayers was studied using a quartz crystal microbalance with dissipation monitoring, which showed enhanced accumulation of the peptide onto the bilayer containing raft components. Microscope observations demonstrated the growth of the aggregates formed from the membrane‐adsorbed hIAPP. The examination of the membrane interfaces revealed that hIAPP aggregates retained the ability to associate with the membranes during the aggregation process, resulting in insertion of the aggregates into the bilayers. We also report the inhibitory effect of insulin on the hIAPP deposition. These findings demonstrate the aggregation of hIAPP at the membrane interfaces leading to amyloid deposits associated with the membrane and suggest a role for insulin in hIAPP deposition. A presumed mechanism regulating hIAPP deposition at the membrane interfaces is discussed.</p> </abstract> … (more)
- Is Part Of:
- FEBS journal. Volume 281:Number 11(2014)
- Journal:
- FEBS journal
- Issue:
- Volume 281:Number 11(2014)
- Issue Display:
- Volume 281, Issue 11 (2014)
- Year:
- 2014
- Volume:
- 281
- Issue:
- 11
- Issue Sort Value:
- 2014-0281-0011-0000
- Page Start:
- 2597
- Page End:
- 2612
- Publication Date:
- 2014-04-30
- Subjects:
- Biochemistry -- Periodicals
Molecular biology -- Periodicals
Pathology, Molecular -- Periodicals
572 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=01038983-000000000-00000 ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=ejb ↗
http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=ejb ↗ - DOI:
- 10.1111/febs.12807 ↗
- Languages:
- English
- ISSNs:
- 1742-464X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3901.578500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4027.xml