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ABSTRACT: Background
CKD is associated with the loss of functional nephr ons, leading to increased mechanical and metabolic stress in the remaining cells, particularly for cells constituting the filtration barrier, such as podocytes. The failure of podocytes to mount an adequate stress response can lead to further nephron loss and disease progression. However, the mechanisms that regulate this degenerative process in the kidney are unknown.Methods
We combined in vitro, in vivo, and organ-on-chip approaches to identify the RE1-silencing transcription factor (REST), a repressor of neuronal genes during embryonic development, as a central regulator of podocyte adaptation to injury and aging.Results
Mice with a specific deletion of REST in podocytes exhibit a
SUBMITTER: Magassa S
PROVIDER: S-EPMC8455262 | biostudies-literature | 2021 Aug
REPOSITORIES: biostudies-literature