Molecular biology and cell biology of the kidney have seen remarkable devel
opment in recent years. Three major cell lineages, endothelial, epithelial,
and fibroblastic, can be traced in the kidney, with high degrees of functi
onal specialization in the different nephron segments. Ischemic, toxic or i
mmunological damage has varying impact on glomerular, tubular and interstit
ial cell populations, often with a major contribution from infiltrating leu
kocytes. Inflammatory, proliferative, repair and degenerative processes pre
viously recognized and studied in renal biopsies are now interpreted at a m
olecular level, with implications for the diagnosis and treatment of kidney
diseases. A host of cellular mediators have been identified, allowing prel
iminary testing of inhibitors, antagonists and novel pharmacological agents
. Gene targeting and manipulation hold promise for the treatment of disorde
rs until now believed to be relentlessly progressive, including new approac
hes to renal allograft and xenograft.