نتایج جستجو برای: islet amyloid polypeptide

تعداد نتایج: 80109  

Journal: :Diabetes 2003
Alexandra E Butler Juliette Janson Walter C Soeller Peter C Butler

Nondiabetic obese humans adapt to insulin resistance by increasing beta-cell mass. In contrast, obese humans with type 2 diabetes have an approximately 60% deficit in beta-cell mass. Recent studies in rodents reveal that beta-cell mass is regulated, increasing in response to insulin resistance through increased beta-cell supply (islet neogenesis and beta-cell replication) and/or decreased beta-...

2007
Chang-jiang Huang Leena Haataja Tatyana Gurlo Alexandra E. Butler Xiuju Wu Walter C. Soeller Peter C. Butler

Huang C-j, Haataja L, Gurlo T, Butler AE, Wu X, Soeller WC, Butler PC. Induction of endoplasmic reticulum stress-induced -cell apoptosis and accumulation of polyubiquitinated proteins by human islet amyloid polypeptide. Am J Physiol Endocrinol Metab 293: E1656–E1662, 2007. First published October 2, 2007; doi:10.1152/ajpendo.00318.2007.—The islet in type 2 diabetes is characterized by an 60% -c...

2010
Jacqueline F. Aitken Kerry M. Loomes David W. Scott Shivanand Reddy Anthony R.J. Phillips Gordana Prijic Chathurini Fernando Shaoping Zhang Ric Broadhurst Phil L'Huillier Garth J.S. Cooper

OBJECTIVE Aggregation of human amylin/islet amyloid polypeptide (hA/hIAPP) into small soluble beta-sheet-containing oligomers is linked to islet beta-cell degeneration and the pathogenesis of type 2 diabetes. Here, we used tetracycline, which modifies hA/hIAPP oligomerization, to probe mechanisms whereby hA/hIAPP causes diabetes in hemizygous hA/hIAPP-transgenic mice. RESEARCH DESIGN AND METH...

2012
Chris T. Middleton Peter Marek Ping Cao Chi-cheng Chiu Sadanand Singh Ann Marie Woys Juan J. de Pablo Daniel P. Raleigh Martin T. Zanni

Amyloid formation has been implicated in the pathology of over 20 human diseases, but the rational design of amyloid inhibitors is hampered by a lack of structural information about amyloid-inhibitor complexes. We use isotope labelling and two-dimensional infrared spectroscopy to obtain a residue-specific structure for the complex of human amylin (the peptide responsible for islet amyloid forma...

Journal: :Experimental Diabetes Research 2008
Lucie Khemtémourian J. Antoinette Killian Jo W. M. Höppener Maarten F. M. Engel

The presence of fibrillar protein deposits (amyloid) of human islet amyloid polypeptide (hIAPP) in the pancreatic islets of Langerhans is thought to be related to death of the insulin-producing islet beta-cells in type 2 diabetes mellitus (DM2). The mechanism of hIAPP-induced beta-cell death is not understood. However, there is growing evidence that hIAPP-induced disruption of beta-cell membran...

2014
Johan F. Paulsson Johnny Ludvigsson Annelie Carlsson Rosaura Casas Gun Forsander Sten A. Ivarsson Ingrid Kockum Åke Lernmark Claude Marcus Bengt Lindblad Gunilla T. Westermark

AIMS/HYPOTHESIS Islet amyloid polypeptide (IAPP) is a beta cell hormone secreted together with insulin upon glucose stimulation. IAPP participates in normal glucose regulation, but IAPP is also known for its ability to misfold and form islet amyloid. Amyloid fibrils form through smaller cell toxic intermediates and deposited amyloid disrupts normal islet architecture. Even though IAPP and amylo...

2016
Lucie Caillon Anais R. F. Hoffmann Alexandra Botz Lucie Khemtemourian

Human islet amyloid polypeptide (hIAPP) is the major component of the amyloid deposits found in the pancreatic islets of patients with type 2 diabetes mellitus (T2DM). Mature hIAPP, a 37-aa peptide, is natively unfolded in its monomeric state but forms islet amyloid in T2DM. In common with other misfolded and aggregated proteins, amyloid formation involves aggregation of monomers of hIAPP into ...

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