The role of urothelial PIEZO ion channels in urinary function
- 1Baylor College of Medicine, Howard Hughes Medical Institute (HHMI)
Abstract
The urothelium is increasingly recognized as a dynamic sensory interface that contributes to the regulation of urinary tract function. Mechanosensitive PIEZO ion channels expressed by urothelial cells have been proposed to play important roles in bladder fullness sensation and urinary reflexes. However, the functional contribution of urothelial PIEZO channels to these processes remains unclear. Here, we investigated the consequences of urothelial Piezo1 and Piezo2 deletion using the commonly used Upk2-cre transgenic line. Surprisingly, combined deletion of urothelial PIEZO channels did not alter urinary behavior, and mice lacking urothelial PIEZO1/2 exhibited normal bladder pressure-volume relationships, indicating preserved bladder filling and voiding function. Notably, Upk2-cre; Piezo1fl/fl mice displayed enhanced external urethral sphincter reflex activity during voiding, suggesting that loss of PIEZO1 from cells targeted by Upk2-cre may influence sensory signaling outside of the bladder urothelium. Consistent with this possibility, we identified substantial off-target Cre expression in dorsal root ganglia. These findings demonstrate that the Upk2-cre line is not restricted to the urothelium and therefore raises important considerations for interpreting associated phenotypes attributed specifically to urothelial gene deletion. Biologically, this raises the possibility that PIEZO1 does not influence bladder pressure-volume handling but might contribute to urinary reflexes.
Related
- Development of iPSC-derived urothelial organoids towards investigating the effect of hormones on host-defense to urinary tract infections
- Urinary TERT promoter mutations as non-invasive biomarkers for the comprehensive detection of urothelial cancer
- Development of Sensitive Droplet Digital PCR Assays for Detecting Urinary TERT Promoter Mutations as Non-Invasive Biomarkers for Detection of Urothelial Cancer
- Gain of Function Cytolysin Variant Expressed by Clinically Isolated Urinary Enterococcus faecalis
- Right Place, Right Function: The Contribution of Subcellular Localization to the Physiological Impact of TRPM2 Channels.
BibTeX
@misc{hamed2026role,
title = {{The role of urothelial PIEZO ion channels in urinary function}},
author = {Y. M. F. Hamed and M. A. Odem and S. Pendyala and T. B. Kwok and K. L. Marshall},
howpublished = {bioRxiv},
year = {2026},
month = oct,
doi = {10.64898/2026.10.10.758063},
url = {https://www.biorxiv.org/content/10.64898/2026.10.10.758063v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - The role of urothelial PIEZO ion channels in urinary function
AU - Y. M. F. Hamed
AU - M. A. Odem
AU - S. Pendyala
AU - T. B. Kwok
AU - K. L. Marshall
PY - 2026
DA - 2026/10/10
PB - bioRxiv
DO - 10.64898/2026.10.10.758063
UR - https://www.biorxiv.org/content/10.64898/2026.10.10.758063v1
AB - The urothelium is increasingly recognized as a dynamic sensory interface that contributes to the regulation of urinary tract function. Mechanosensitive PIEZO ion channels expressed by urothelial cells have been proposed to play important roles in bladder fullness sensation and urinary reflexes. However, the functional contribution of urothelial PIEZO channels to these processes remains unclear. Here, we investigated the consequences of urothelial Piezo1 and Piezo2 deletion using the commonly used Upk2-cre transgenic line. Surprisingly, combined deletion of urothelial PIEZO channels did not alter urinary behavior, and mice lacking urothelial PIEZO1/2 exhibited normal bladder pressure-volume relationships, indicating preserved bladder filling and voiding function. Notably, Upk2-cre; Piezo1fl/fl mice displayed enhanced external urethral sphincter reflex activity during voiding, suggesting that loss of PIEZO1 from cells targeted by Upk2-cre may influence sensory signaling outside of the bladder urothelium. Consistent with this possibility, we identified substantial off-target Cre expression in dorsal root ganglia. These findings demonstrate that the Upk2-cre line is not restricted to the urothelium and therefore raises important considerations for interpreting associated phenotypes attributed specifically to urothelial gene deletion. Biologically, this raises the possibility that PIEZO1 does not influence bladder pressure-volume handling but might contribute to urinary reflexes.
ER -