TY - JOUR
T1 - A Protocol to Enhance INS1E and MIN6 Functionality—The Use of Theophylline
AU - Groot Nibbelink, Milou
AU - Marchioli, Giulia
AU - Moroni, Lorenzo
AU - Karperien, Marcel
AU - van Apeldoorn, Aart
PY - 2016
Y1 - 2016
N2 - In vitro research in the field of type I diabetes is frequently limited by the availability of a functional model for islets of Langerhans. This method shows that by the addition of theophylline to the glucose buffers, mouse insulinoma MIN6 and rat insulinoma INS1E pseudo-islets can serve as a model for islets of Langerhans for in vitro research. The effect of theophylline is dose- and cell line-dependent, resulting in a minimal stimulation index of five followed by a rapid return to
baseline insulin secretion by reducing glucose concentrations after a first high glucose stimulation. This protocol solves issues concerning in vitro research for type I diabetes as donors and the availability of primary islets of Langerhans are limited. To avoid the limitations of using human donor material, cell lines represent a valid alternative. Many different cell lines have been reported, but the lack of reproducible responsiveness to glucose stimulation remains a challenge.
AB - In vitro research in the field of type I diabetes is frequently limited by the availability of a functional model for islets of Langerhans. This method shows that by the addition of theophylline to the glucose buffers, mouse insulinoma MIN6 and rat insulinoma INS1E pseudo-islets can serve as a model for islets of Langerhans for in vitro research. The effect of theophylline is dose- and cell line-dependent, resulting in a minimal stimulation index of five followed by a rapid return to
baseline insulin secretion by reducing glucose concentrations after a first high glucose stimulation. This protocol solves issues concerning in vitro research for type I diabetes as donors and the availability of primary islets of Langerhans are limited. To avoid the limitations of using human donor material, cell lines represent a valid alternative. Many different cell lines have been reported, but the lack of reproducible responsiveness to glucose stimulation remains a challenge.
U2 - 10.3390/ijms17091532
DO - 10.3390/ijms17091532
M3 - Article
SN - 1661-6596
VL - 17
JO - International journal of molecular sciences
JF - International journal of molecular sciences
IS - 1532
M1 - 1532
ER -