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Sökning: onr:"swepub:oai:lup.lub.lu.se:29f386d9-ebb9-46e6-9870-57ecf5aa8998" > DPP-4 is expressed ...

DPP-4 is expressed in human pancreatic beta cells and its direct inhibition improves beta cell function and survival in type 2 diabetes

Bugliani, Marco (författare)
University of Pisa
Syed, Farooq (författare)
University of Pisa
Paula, Flavia M.M. (författare)
Université Libre de Bruxelles (ULB)
visa fler...
Omar, Bilal A. (författare)
Lund University,Lunds universitet,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Department of Clinical Sciences, Lund,Faculty of Medicine
Suleiman, Mara (författare)
University of Pisa
Mossuto, Sandra (författare)
University of Pisa
Grano, Francesca (författare)
University of Pisa
Cardarelli, Francesco (författare)
Scuola Normale Superiore di Pisa
Boggi, Ugo (författare)
University of Pisa
Vistoli, Fabio (författare)
University of Pisa
Filipponi, Franco (författare)
University of Pisa
De Simone, Paolo (författare)
University of Pisa
Marselli, Lorella (författare)
University of Pisa
De Tata, Vincenzo (författare)
University of Pisa
Ahren, Bo (författare)
Lund University,Lunds universitet,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Department of Clinical Sciences, Lund,Faculty of Medicine
Eizirik, Decio L. (författare)
Université Libre de Bruxelles (ULB)
Marchetti, Piero (författare)
University of Pisa
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 (creator_code:org_t)
Elsevier BV, 2018
2018
Engelska.
Ingår i: Molecular and Cellular Endocrinology. - : Elsevier BV. - 0303-7207. ; 473, s. 186-193
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • It has been reported that the incretin system, including regulated GLP-1 secretion and locally expressed DPP-4, is present in pancreatic islets. In this study we comprehensively evaluated the expression and role of DPP-4 in islet alpha and beta cells from non-diabetic (ND) and type 2 diabetic (T2D) individuals, including the effects of its inhibition on beta cell function and survival. Isolated islets were prepared from 25 ND and 18 T2D organ donors; studies were also performed with the human insulin-producing EndoC-βH1 cells. Morphological (including confocal microscopy), ultrastructural (electron microscopy, EM), functional (glucose-stimulated insulin secretion), survival (EM and nuclear dyes) and molecular (RNAseq, qPCR and western blot) studies were performed under several different experimental conditions. DPP-4 co-localized with glucagon and was also expressed in human islet insulin-containing cells. Furthermore, DPP-4 was expressed in EndoC-βH1 cells. The proportions of DPP-4 positive alpha and beta cells and DPP-4 gene expression were significantly lower in T2D islets. A DPP-4 inhibitor protected ND human beta cells and EndoC-βH1 cells against cytokine-induced toxicity, which was at least in part independent from GLP1 and associated with reduced NFKB1 expression. Finally, DPP-4 inhibition augmented glucose-stimulated insulin secretion, reduced apoptosis and improved ultrastructure in T2D beta cells. These results demonstrate the presence of DPP-4 in human islet alpha and beta cells, with reduced expression in T2D islets, and show that DPP-4 inhibition has beneficial effects on human ND and T2D beta cells. This suggests that DPP-4, besides playing a role in incretin effects, directly affects beta cell function and survival.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Nyckelord

Apoptosis
Beta cells
Cytokines
DPP-4
MK-0626
Type 2 diabetes

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