Damage of the glomerular filtration barrier leads to proteinuria and progre
ssive renal failure. Several independent lines of research have implicated
the glomerular epithelial cell (GEC) as a key player in initiation and prop
agation of pathways leading to glomerulosclerosis. A growing number of mole
cules activated in this process have been identified. To further define the
ir cellular function, manipulation of these molecules using pharmacological
or genetic approaches in tissue culture systems are required. In this stud
y, strategies for altering GEC gene expression by transient and stable tran
sfection of fluorescence labeled proteins will be presented and discussed.
The insight gained through these and comparable systems should allow a deta
iled dissection of the molecular pathways active in GEC function and failur
e.