Source:http://linkedlifedata.com/resource/pubmed/id/21641386
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2011-6-6
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pubmed:abstractText |
Amyloid deposition and reduced ?-cell mass are pathological hallmarks of the pancreatic islet in type 2 diabetes; however, whether the extent of amyloid deposition is associated with decreased ?-cell mass is debated. We investigated the possible relationship and, for the first time, determined whether increased islet amyloid and/or decreased ?-cell area quantified on histological sections is correlated with increased ?-cell apoptosis. Formalin-fixed, paraffin-embedded human pancreas sections from subjects with (n = 29) and without (n = 39) diabetes were obtained at autopsy (64 ± 2 and 70 ± 4 islets/subject, respectively). Amyloid and ? cells were visualized by thioflavin S and insulin immunolabeling. Apoptotic ? cells were detected by colabeling for insulin and by TUNEL. Diabetes was associated with increased amyloid deposition, decreased ?-cell area, and increased ?-cell apoptosis, as expected. There was a strong inverse correlation between ?-cell area and amyloid deposition (r = -0.42, P < 0.001). ?-Cell area was selectively reduced in individual amyloid-containing islets from diabetic subjects, compared with control subjects, but amyloid-free islets had ?-cell area equivalent to islets from control subjects. Increased amyloid deposition was associated with ?-cell apoptosis (r = 0.56, P < 0.01). Thus, islet amyloid is associated with decreased ?-cell area and increased ?-cell apoptosis, suggesting that islet amyloid deposition contributes to the decreased ?-cell mass that characterizes type 2 diabetes.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/K01 DK074404-05,
http://linkedlifedata.com/resource/pubmed/grant/K01-DK74404,
http://linkedlifedata.com/resource/pubmed/grant/K99 DK080945-02,
http://linkedlifedata.com/resource/pubmed/grant/K99-DK80945,
http://linkedlifedata.com/resource/pubmed/grant/P30-DK17047,
http://linkedlifedata.com/resource/pubmed/grant/R01-DK7599,
http://linkedlifedata.com/resource/pubmed/grant/T32-DK07247
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1525-2191
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pubmed:author |
pubmed-author:Aston-MourneyKathrynK,
pubmed-author:CarrDarcy BDB,
pubmed-author:FlignerCorinne LCL,
pubmed-author:HullRebecca LRL,
pubmed-author:JurgensCatherine ACA,
pubmed-author:KahnSteven ESE,
pubmed-author:SubramanianShoba LSL,
pubmed-author:ToukatlyMirna NMN,
pubmed-author:UdayasankarJayalakshmiJ,
pubmed-author:WestermarkGunilla TGT,
pubmed-author:WestermarkPerP,
pubmed-author:ZraikaSakenehS
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pubmed:copyrightInfo |
Copyright © 2011 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
178
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2632-40
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pubmed:meshHeading |
pubmed-meshheading:21641386-Adult,
pubmed-meshheading:21641386-Aged,
pubmed-meshheading:21641386-Aged, 80 and over,
pubmed-meshheading:21641386-Amyloid,
pubmed-meshheading:21641386-Apoptosis,
pubmed-meshheading:21641386-Case-Control Studies,
pubmed-meshheading:21641386-Demography,
pubmed-meshheading:21641386-Diabetes Mellitus, Type 2,
pubmed-meshheading:21641386-Female,
pubmed-meshheading:21641386-Humans,
pubmed-meshheading:21641386-Insulin-Secreting Cells,
pubmed-meshheading:21641386-Male,
pubmed-meshheading:21641386-Middle Aged,
pubmed-meshheading:21641386-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
?-cell loss and ?-cell apoptosis in human type 2 diabetes are related to islet amyloid deposition.
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pubmed:affiliation |
Division of Metabolism, Endocrinology and Nutrition, Veterans Affairs Puget Sound Health Care System and University of Washington, Seattle, Washington, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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