bioRxivGeneticsPreprint
Non-canonical Wnt signaling triggered by WNT2B drives adrenal aldosterone production
Kleiton Silva BorgesiD, Donald W. LittleiD, Taciani de Almeida MagalhãesiD, Claudio Henrique T. RibeiroiD, Typhanie DumontetiD, Christopher Ryan LaPenseeiD, Kaitlin J. BashamiD, Aishwarya Seth, Svetlana AzovaiD, Nick A. GuagliardoiD, Paula Q. BarrettiD, Mesut BerberiD, Amy E. O’ConnelliD, Adina F. TurcuiD, Antônio Marcondes LerárioiD, Dipika R. MohaniD, William E. RaineyiD, Diana L. CarloneiD, Joel N. HirschhorniD, Adrian N. SaliciD, David T. BreaultiD, Gary Douglas HammeriD
Abstract
The steroid hormone aldosterone, produced by the zona glomerulosa (zG) of the adrenal gland, is a master regulator of plasma electrolytes and blood pressure. While aldosterone control by the renin-angiotensin system is well understood, other key regulatory factors have remained elusive. Here, we replicated a prior association between a non-coding variant in WNT2B and an increased risk of primary aldosteronism, a prevalent and debilitating disease caused by excessive aldosterone production. We further show that in both mice and humans, WNT2B is expressed in the mesenchymal capsule surrounding the adrenal cortex, in close proximity to the zG. Global loss of Wnt2b in the mouse results in a dysmorphic and hypocellular zG, with impaired aldosterone production. Similarly, humans harboring WNT2B loss-of-function mutations develop a novel form of Familial Hyperreninemic Hypoaldosteronism, designated here as Type 4. Additionally, we demonstrate that WNT2B signals by activating the non-canonical Wnt/planar cell polarity pathway. Our findings identify WNT2B as a key regulator of zG function and aldosterone production with important clinical implications. HighlightsO_LIWNT2B variant is associated with increased risk for primary aldosteronism C_LIO_LIWnt2b knock-out mice show defects in adrenal morphology C_LIO_LIWnt2b knock-out mice have hyperreninemic hypoaldosteronism C_LIO_LIWNT2B activates non-canonical Wnt/planar cell polarity signaling C_LIO_LIWNT2B deficiency causes a new form of familial hyperreninemic hypoaldosteronism C_LI
- organism: mouse
- organism: human
- assay: bulk RNA-seq
- research focus: gene regulatory network inference
- research focus: differential expression
- approach: statistical model
- approach: experimental assay
- Citations
- 11
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Rho-ROCK signaling and α-Catenin mediate β-Catenin-driven hyperplasia in the adrenal via adherens junctions
Mesut Berber, Betül Haykir, … David T. Breault·Journal of Clinical InvestigationPeer-reviewed·Jan 27, 2026
- ClC-2 contributes to hypotonicity-induced adrenal aldosterone secretion
Marina Volkert, Hoang An Dinh, … Gabriel Stölting·Acta PhysiologicaPeer-reviewed·Jan 28, 2026
- Intrarenal Generation of Aldosterone Contributes to Ischemia-Induced Hypertension and Nephropathy in Mice
Ziwei Fu, Chang‐Jiang Zou, … Tianxin Yang·bioRxiv·Aug 24, 2025
- Somatic Mutations in MCOLN3 in Aldosterone-Producing Adenomas cause Primary Aldosteronism.
Desmaré van Rooyen, Sascha Bandulik, … Juilee Rege·bioRxiv·Oct 20, 2024
- Sexually dimorphic interzonal crosstalk reshapes the adrenal cortex in response to pathophysiological challenges
Nicolò Faedda, Alaa B Abdellatif, … Maria‐Christina Zennaro·bioRxiv·Sep 5, 2025
- Zinc transporter somatic gene mutations cause primary aldosteronism
Juilee Rege, Kazutaka Nanba, … William E. Rainey·bioRxiv·Jul 25, 2022