Stable HeLa cell line for use in anti-diabetic and anti-obesity drug screening and trials
The technology
We've developed a robust easy-to-use test that provides a useful read-out for insulin sensitivity and screening potential of antagonistic or synergistic small molecules or other drugs.
When treating diabetes with insulin, a major consequence is an increase in the rate of glucose transport into fat and muscle. This happens through regulated trafficking of the facilitative glucose transporter GLUT4 from insulin-sensitive intracellular stores to the plasma membrane, a process termed 'translocation'. Our scientists have developed an assay system to allow 'hits' for anti-diabetic and anti-obesity drugs to be identified quickly and cheaply, ready for further analysis
Researchers at Strathclyde employ a stable HeLa cell line engineered to express HA-GLUT4-GFP. This was driven by a need to establish a cell line that can be readily genetically manipulated and imaged, and by a lack of reagents that can target endogenous GLUT4 specifically at the plasma membrane. HA-GLUT4-GFP is widely used in studies of GLUT4 trafficking; it has been extensively characterised and validated. GFP reports on the distribution of GLUT4 and the HA-epitope (only accessible to anti-HA added to the media of non-permeabilised cells) allows quantification of levels of GLUT4 in the plasma membrane. GFP also reports on total levels of GLUT4.
This assay lends itself to FACS analysis and can also be multiplexed in 96-well plates.Anti-diabetic and anti-obesity drug screening and trials.