scholarly journals Cellular characterization of pituitary adenoma cell line (AtT20 cell) transfected with insulin, glucose transporter type 2 (GLUT2) and glucokinase genes: Insulin secretion in response to physiological concentrations of glucose

Diabetologia ◽  
1998 ◽  
Vol 41 (12) ◽  
pp. 1492-1501 ◽  
Author(s):  
S. Motoyoshi ◽  
T. Shirotani ◽  
E. Araki ◽  
K. Sakai ◽  
K. Kaneko ◽  
...  
2018 ◽  
Vol 9 ◽  
Author(s):  
Matteo Pigni ◽  
Devika Ashok ◽  
Mathias Stevanin ◽  
Hans Acha-Orbea
Keyword(s):  

1998 ◽  
Vol 9 (2) ◽  
pp. 169-184 ◽  
Author(s):  
Long Jin ◽  
Elzbieta Kulig ◽  
Xiang Qian ◽  
Bernd W. Scheithauer ◽  
Norman L. Eberhardt ◽  
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Vol 91 (2) ◽  
pp. 401-404 ◽  
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Céline Druet ◽  
Nadia Tubiana-Rufi ◽  
Didier Chevenne ◽  
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1990 ◽  
Vol 46 (6) ◽  
pp. 1059-1065 ◽  
Author(s):  
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John R. Clamp ◽  
Angela D. Casey ◽  
Christos Paraskeva

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Vol 307 (3) ◽  
pp. G330-G337 ◽  
Author(s):  
Ramona Pais ◽  
Tamara Zietek ◽  
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Hannelore Daniel ◽  
Thomas Skurk

Type 2 diabetes is associated with elevated circulating levels of the chemokine RANTES and with decreased plasma levels of the incretin hormone glucagon-like peptide 1 (GLP-1). GLP-1 is a peptide secreted from intestinal L-cells upon nutrient ingestion. It enhances insulin secretion from pancreatic β-cells and protects from β-cell loss but also promotes satiety and weight loss. In search of chemokines that may reduce GLP-1 secretion we identified RANTES and show that it reduces glucose-stimulated GLP-1 secretion in the human enteroendocrine cell line NCI-H716, blocked by the antagonist Met-RANTES, and in vivo in mice. RANTES exposure to mouse intestinal tissues lowers transport function of the intestinal glucose transporter SGLT1, and administration in mice reduces plasma GLP-1 and GLP-2 levels after an oral glucose load and thereby impairs insulin secretion. These data show that RANTES is involved in altered secretion of glucagon-like peptide hormones most probably acting through SGLT1, and our study identifies the RANTES-receptor CCR1 as a potential target in diabetes therapy.


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