HNF1B integrates signals in a feed-forward loop driving kidney disease progression
Summary
Chronic kidney disease (CKD), which affects more than 10% of the global population, may continue to progress even after the triggering insult has resolved, suggesting the involvement of self-sustaining mechanisms that remain poorly understood. Here, we identify this molecular circuitry, centered on the transcription factor HNF1B, a key regulator of renal epithelial identity. In adult kidneys, HNF1B loss disrupts epithelial differentiation and quiescence, induces replication stress, and tri
Content
# HNF1B integrates signals in a feed-forward loop driving kidney disease progression
*Published: 2026 Apr 16*
Chronic kidney disease (CKD), which affects more than 10% of the global
population, may continue to progress even after the triggering insult has
resolved, suggesting the involvement of self-sustaining mechanisms that remain
poorly understood. Here, we identify this molecular circuitry, centered on the
transcription factor HNF1B, a key regulator of renal epithelial identity. In
adult kidneys, HNF1B loss disrupts epithelial differentiation and quiescence,
induces replication stress, and triggers CKD. Conversely, CKD itself
epigenetically suppresses HNF1B activity, creating a vicious cycle that
amplifies disease progression. In a cohort of 900 patients, lower HNF1B activity
correlated with greater CKD severity, linking this mechanism to common forms of
the disease. These findings unify rare Mendelian and common complex kidney
disorders and identify HNF1B loss as a driver of CKD.
DOI: 10.1126/science.aea3219