scholarly journals The p21-activated kinase (PAK1) is involved in diet-induced beta cell mass expansion and survival in mice and human islets

Diabetologia ◽  
2016 ◽  
Vol 59 (10) ◽  
pp. 2145-2155 ◽  
Author(s):  
Miwon Ahn ◽  
Stephanie M. Yoder ◽  
Zhanxiang Wang ◽  
Eunjin Oh ◽  
Latha Ramalingam ◽  
...  
Diabetologia ◽  
2015 ◽  
Vol 58 (9) ◽  
pp. 2064-2073 ◽  
Author(s):  
Yili Xu ◽  
Xiaojing Wang ◽  
Li Gao ◽  
Jiayu Zhu ◽  
Hui Zhang ◽  
...  

1995 ◽  
Vol 59 (6) ◽  
pp. 817-820 ◽  
Author(s):  
A. M. DAVALLI ◽  
Y. OGAWA ◽  
C. RICORDI ◽  
D. W. SCHARP ◽  
S. BONNER-WEIR ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Lucien Marchand ◽  
Audrey Jalabert ◽  
Emmanuelle Meugnier ◽  
Kathleen Van den Hende ◽  
Nicole Fabien ◽  
...  

Background.The use of miRNAs as biomarkers for Type 1 Diabetes (T1D) risk is attractive as T1D is usually diagnosed in front of acute symptoms. As miR-375 is highly expressed in the endocrine pancreas, we postulated that its circulating level might reflect beta cell alterations and might be altered in the blood of T1D patients recently diagnosed.Methods.Sera were obtained from 22 T1D children at onset of the disease, before subcutaneous insulin treatment, and from 10 nondiabetic pediatric controls. MiR-375 seric level was quantified by stem-loop RT-PCR-based assay. MiRNAs regulations in isolated human islets in response to high glucose concentrations were determined by TaqMan Low-Density Array.Results.The abundance of miR-375, among the 410 miRNAs detected in human islets, mirrored its well-established role in rodent islet biology. Upregulated miRNAs targeted genes involved in islet homeostasis and regulation of beta cell mass. Downregulated miRNAs, including miR-375, were involved in pancreas secretion and protein turnover. Seric level of miR-375 was lower in T1D children versus age-matched controls, without any correlations with HbA1c, glycaemia, and number of autoantibodies.Conclusion.Altered circulating level of miR-375 at onset of T1D might be a general biomarker of metabolic alterations and inflammation associated with the disease.


Diabetologia ◽  
2006 ◽  
Vol 49 (12) ◽  
pp. 2910-2919 ◽  
Author(s):  
M. A. Lipsett ◽  
E. B. Austin ◽  
M. L. Castellarin ◽  
J. Lemay ◽  
L. Rosenberg

2020 ◽  
Author(s):  
Ada Admin ◽  
Mijke Buitinga ◽  
Christian M.Cohrs ◽  
Wael A.Eter ◽  
Lieke Claessens-Joosten ◽  
...  

GLP-1R imaging with radiolabelled exendin has proven to be a powerful tool to quantify beta-cell mass (BCM) <i>in vivo</i>. As GLP-1R expression is thought to be influenced by glycemic control, we examined the effect of blood glucose levels on GLP-1R-mediated exendin uptake in both murine and human islets and its implications for BCM quantification. Periods of hyperglycemia significantly reduced exendin uptake in murine and human islets, which was paralleled by a reduction in GLP-1R expression. Detailed mapping of the tracer uptake and insulin and GLP-1R expression conclusively demonstrated that the observed reduction in tracer uptake directly correlates to GLP-1R expression levels. Importantly, the linear correlation between tracer uptake and beta-cell area was maintained in spite of the reduced GLP-1R expression levels. Subsequent normalization of blood glucose levels restored absolute tracer uptake and GLP-1R expression in beta-cells and the observed loss in islet volume was halted. <p>This manuscript emphasizes the potency of nuclear imaging techniques to monitor receptor regulation non-invasively. Our findings have significant implications for clinical practice, indicating that blood glucose levels should be near-normalized for at least three weeks prior to GLP-1R agonist treatment or quantitative radiolabeled exendin imaging for BCM analysis.</p>


1995 ◽  
Vol 59 (6) ◽  
pp. 817-820 ◽  
Author(s):  
A. M. DAVALLI ◽  
Y. OGAWA ◽  
C. RICORDI ◽  
D. W. SCHARP ◽  
S. BONNER-WEIR ◽  
...  

PLoS ONE ◽  
2012 ◽  
Vol 7 (8) ◽  
pp. e41976 ◽  
Author(s):  
Xiaohong Wu ◽  
Qinfeng Zhang ◽  
Xiaojing Wang ◽  
Jiayu Zhu ◽  
Kuangfeng Xu ◽  
...  

2010 ◽  
Vol 90 ◽  
pp. 1001
Author(s):  
L. Marzban ◽  
Z. Ao ◽  
T. J. Kieffer ◽  
M. Meloche ◽  
N. Safikhan ◽  
...  

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