Activin A stimulates insulin secretion in cultured human pancreatic islets

被引:0
作者
P. Florio
S. Luisi
P. Marchetti
R. Lupi
L. Cobellis
C. Falaschi
H. Sugino
R. Navalesi
A. R. Genazzani
F. Petraglia
机构
[1] University of Pisa,Department of Reproductive Medicine and Child Development, Section of Obstetrics and Gynecology
[2] University of Pisa,Department of Diabetology
[3] University of Udine,Department of Surgical Sciences
[4] University of Tokushima,Division of Molecular Cytology
来源
Journal of Endocrinological Investigation | 2000年 / 23卷
关键词
Activin A; insulin; human pancreatic islets; glucose;
D O I
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学科分类号
摘要
Activin A is a dimeric glycoprotein showing a high sequence homology with transforming growth factor-ß (TGF-ß) and playing autocrine/ paracrine actions in reproductive tissues. However, since the synthesis of activin is ubiquitous it may have a role in regulating cell growth and differentiation in several tissues. Previous studies showed that activin A is expressed by insulin-positive B cells of human pancreatic islets, and women with gestational diabetes have higher serum activin A levels than healthy pregnant women at the same gestational age. The present study aimed to evaluate the effect of activin A on insulin secretion from cultured human pancreatic islets. With this purpose human pancreatic islets were incubated with varying concentrations of activin A (0.1 to 10.0 nM). In absence of glucose, activin A did not modify insulin secretion at the different concentrations used. In absence of activin A, 8.3 mM and 16.7 mM glucose significantly increased insulin secretion, with a dosedependent pattern. In presence of a non stimulatory concentration of glucose (3.3 mM), activin A significantly increased insulin secretion starting from low concentration (0.1 nM). Furthermore, the addition of activin A to 8.3 mM and 16.7 mM glucose induced an additional effect of the dose-dependent glucose-mediated insulin secretion (p<0.001). The present data could support a role for activin A in human endocrine pancreas in modulating insulin response to different glucose concentrations.
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页码:231 / 234
页数:3
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