Renal gene transfer techniques are being developed as a novel experime
ntal approach to understand the pathogenesis of renal disease and to p
otentially develop new therapeutic tools. We review the currently avai
lable technology to introduce foreign genetic material into renal tiss
ue, i.e., retroviral, adenoviral, and liposomal transfer systems with
their respective advantages and caveats. Today, the transfer efficienc
y of these methods appears to be sufficiently high to study the effect
s of transduced genes on renal function and morphology in rat kidney.
This will allow (i) the elucidation of the function of genes on the co
urse of renal disease in experimental animal models and (ii) the modul
ation of local expression of endogenous genes which presumptively cont
ribute to renal pathology in these models. One strategy to accomplish
this aim is the use of recombinant DNA technology to design antisense
DNA constructs or oligonucleotides, which interfere with the renal exp
ression of target genes. We will also discuss some of the shortcomings
of the currently used techniques with respect to potential therapeuti
c use of gene transfer systems and gene modulation.