Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Physician-Scientist Development
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • In-Press Preview
    • Resource and Technical Advances
    • Clinical Research and Public Health
    • Research Letters
    • Editorials
    • Perspectives
    • Physician-Scientist Development
    • Reviews
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Resource and Technical Advances
  • Clinical Research and Public Health
  • Research Letters
  • Editorials
  • Perspectives
  • Physician-Scientist Development
  • Reviews
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
Functional roles for PIEZO1 and PIEZO2 in urothelial mechanotransduction and lower urinary tract interoception
Marianela G. Dalghi, Wily G. Ruiz, Dennis R. Clayton, Nicolas Montalbetti, Stephanie L. Daugherty, Jonathan M. Beckel, Marcelo D. Carattino, Gerard Apodaca
Marianela G. Dalghi, Wily G. Ruiz, Dennis R. Clayton, Nicolas Montalbetti, Stephanie L. Daugherty, Jonathan M. Beckel, Marcelo D. Carattino, Gerard Apodaca
View: Text | PDF
Research Article Cell biology

Functional roles for PIEZO1 and PIEZO2 in urothelial mechanotransduction and lower urinary tract interoception

  • Text
  • PDF
Abstract

The mechanisms that link visceral mechanosensation to the perception of internal organ status (i.e., interoception) remain elusive. In response to bladder filling, the urothelium releases ATP, which is hypothesized to stimulate voiding function by communicating the degree of bladder fullness to subjacent tissues, including afferent nerve fibers. To determine if PIEZO channels function as mechanosensors in these events, we generated conditional urothelial Piezo1-, Piezo2-, and dual Piezo1/2-knockout (KO) mice. While functional PIEZO1 channels were expressed in all urothelial cell layers, Piezo1-KO mice had a limited phenotype. Piezo2 expression was limited to a small subset of superficial umbrella cells, yet male Piezo2-KO mice exhibited incontinence (i.e., leakage) when their voiding behavior was monitored during their active dark phase. Dual Piezo1/2-KO mice had the most affected phenotype, characterized by decreased urothelial responses to mechanical stimulation, diminished ATP release, bladder hypoactivity in anesthetized Piezo1/2-KO females but not males, and urinary incontinence in both male and female Piezo1/2-KO mice during their dark phase but not inactive light one. Our studies reveal that the urothelium functions in a sex- and circadian rhythm–dependent manner to link urothelial PIEZO1/2 channel–driven mechanotransduction to normal voiding function and behavior, and in the absence of these signals, bladder dysfunction ensues.

Authors

Marianela G. Dalghi, Wily G. Ruiz, Dennis R. Clayton, Nicolas Montalbetti, Stephanie L. Daugherty, Jonathan M. Beckel, Marcelo D. Carattino, Gerard Apodaca

×

Figure 2

Evidence of PIEZO channel–dependent mechanotransduction in bladder urothelium.

Options: View larger image (or click on image) Download as PowerPoint
Evidence of PIEZO channel–dependent mechanotransduction in bladder uroth...
(A–C) Yoda1-stimulated PIEZO1 activation in GCAMP5G-transduced urothelium. (A) Diagram of experimental approach. (B) Example of Yoda1-induced [Ca2+]i increases in Piezo1/2-control or Piezo1/2-KO urothelium. Scale bar: 100 μm. (C) Yoda1-induced changes in [Ca2+]i, normalized to control responses. Data are shown as mean ± SEM (n = 3). Data were analyzed using t tests and significant differences indicated with an asterisk (P ≤ 0.05). (D–F) Piezo channel dependence of poking-induced changes in [Ca2+]i. (D) Diagram depicting experimental approach. (E) Example of poking-induced increase in [Ca2+]i in urothelium transduced with adenovirus encoding GCAMP5G. In the 3 images to the right, the indicated cell (yellow arrow) was poked at 10.0 seconds, and the changes in [Ca2+]i were recorded over the next several seconds. Scale bar: 50 μm. (F) Poking-induced [Ca2+]i changes in randomly selected umbrella cells. Data, normalized to matched controls, are shown as mean ± SEM (n = 3 animals for each group; the value of each animal is the average from 11–14 cells). Data were analyzed using t tests and significant differences indicated with an asterisk (P ≤ 0.05). (G and H) Dependence of serosal ATP release on Piezo expression. (G) Schematic of the experimental setup. (H) Upper panels: ATP release from peeled bladders of the indicated strain of mouse. Both males and females were used in this analysis. The peeled bladders were filled after fraction 3. Bottom panels: The total filling-induced ATP release from the serosal surfaces of peeled bladders was calculated. Data are shown as mean ± SEM (Piezo1-control, n = 5; Piezo1-KO, n = 6; Piezo2-control and Piezo2-KO, n = 3; Piezo1/2-control and Piezo1/2-KO, n = 5). Data were analyzed using t tests and significant differences indicated with a double asterisk (P ≤ 0.01).

Copyright © 2025 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts