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ATP and purinergic receptor–dependent membrane traffic in bladder umbrella cells
Edward C.Y. Wang, … , Lori A. Birder, Gerard Apodaca
Edward C.Y. Wang, … , Lori A. Birder, Gerard Apodaca
Published September 1, 2005
Citation Information: J Clin Invest. 2005;115(9):2412-2422. https://doi.org/10.1172/JCI24086.
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Research Article Cell biology

ATP and purinergic receptor–dependent membrane traffic in bladder umbrella cells

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Abstract

The umbrella cells that line the bladder are mechanosensitive, and bladder filling increases the apical surface area of these cells; however, the upstream signals that regulate this process are unknown. Increased pressure stimulated ATP release from the isolated uroepithelium of rabbit bladders, which was blocked by inhibitors of vesicular transport, connexin hemichannels, ABC protein family members, and nucleoside transporters. Pressure-induced increases in membrane capacitance (a measure of apical plasma membrane surface area where 1 μF ≈ 1 cm2) were inhibited by the serosal, but not mucosal, addition of apyrase or the purinergic receptor antagonist PPADS. Upon addition of purinergic receptor agonists, increased capacitance was observed even in the absence of pressure. Moreover, knockout mice lacking expression of P2X2 and/or P2X3 receptors failed to show increases in apical surface area when exposed to hydrostatic pressure. Treatments that prevented release of Ca2+ from intracellular stores or activation of PKA blocked ATPγS-stimulated changes in capacitance. These results indicate that increased hydrostatic pressure stimulates release of ATP from the uroepithelium and that upon binding to P2X and possibly P2Y receptors on the umbrella cell, downstream Ca2+ and PKA second messenger cascades may act to stimulate membrane insertion at the apical pole of these cells.

Authors

Edward C.Y. Wang, Jey-Myung Lee, Wily G. Ruiz, Elena M. Balestreire, Maximilian von Bodungen, Stacey Barrick, Debra A. Cockayne, Lori A. Birder, Gerard Apodaca

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Figure 5

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Localization of P2X3 in the uroepithelium and responses to pressure chan...
Localization of P2X3 in the uroepithelium and responses to pressure changes in P2X2- and P2X3-knockout mice. (A and B) Localization of P2X3 in cryosections of rabbit bladder uroepithelium. (A) P2X3 staining is shown in green, and the umbrella cells (UC) are marked with arrows. (B) Composite image with P2X3 staining shown in green, rhodamine-phalloidin–labeled actin in red, and Topro-3–labeled (Molecular Probes) nuclei in blue. (C) Whole mounted rabbit uroepithelium showing the distribution of the nuclei (blue) and P2X3 (green). The image is a 3-dimensional reconstruction of a Z series collected with a confocal microscope. The image was tilted around the x axis to emphasize the 3-dimensional aspect of the image. The grid is a 3-dimensional scale bar, with each side of the square approximately equivalent to 12.5 μm. (D) Bladders from mice of the indicated strains were mounted in Ussing stretch chambers, the pressure was increased at t = 0, and the capacitance was recorded. Data shown are mean ± SEM (n ≥ 3). *Statistically significant difference (P < 0.05) relative to the appropriate control.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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