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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
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Research Article Cell biology

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

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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

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Figure 1

Expression and distribution of Piezo1 and Piezo2 in mouse bladder urothelium.

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Expression and distribution of Piezo1 and Piezo2 in mouse bladder urothe...
(A) Distribution of Piezo1 (signal dots in red, surrounded by yellow circles) and uroplakin 3A (Upk3a) (green) assessed using FISH. Urothelial boundary is outlined with white dashed lines (lumen indicated by red arrowheads), scale bars: 50 μm. (B) Western blot analysis of PIEZO1-tdT expression in urothelium (Ut) or detrusor (D) fractions taken from Piezo1+/+ (lanes 1 and 3) or Piezo1tdT/tdT (lanes 2 and 4) mouse bladders. (C) Distribution of PIEZO1-tdT in bladder wall, scale bar: 100 μm. (D and E) Localization of PIEZO1-tdT with respect to the actin cytoskeleton or claudin-8 (CLDN8). Apical surface of umbrella cells are marked with white dashed lines, arrows point to the location of the junctional complex, closed white circles indicate umbrella cell nuclei, and the region of tissue in the yellow dashed box is magnified 2.9-fold (2.9×) in the insets. Scale bars: 20 μm. (F) Piezo2 (red) and Upk3a (green) expression in mouse bladder urothelium defined using FISH. Arrows mark the position of Piezo2-expressing umbrella cells. The boxed region, indicated by a dashed yellow line, is magnified 14-fold (14×) in the insets. The larger panel is a photomerge of 11 images, collected using a wide-field microscope. The area bound by the rectangular box includes a stitching error when the samples were merged. Scale bar: 200 μm. (G) Expression of tdT in Piezo2Cre-IRES-GFP mice mated with Ai9 reporter mice. In the confocal images at the left and at the center, a single tdT-positive umbrella cell is located at the tip of a bladder rugae (also note tdT+ fibroblasts in LP). The region of the yellow dashed line is magnified 2-fold (2×) in the images below. Confocal images to the right show tdT-positive umbrella cells, viewed en face in whole-mounted bladder tissue. Examples of the regional expression of tdT-positive umbrella cells (and the tight junction protein TJP1) from the dome, equator, and neck region of the bladder are shown. All confocal images are 3D reconstructions of 32–48 optical sections. Scale bars: 100 μm. DIC, differential interference contrast; LP, lamina propria; L, lumen; Ut, urothelium.

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