May 1994
Volume 35, Issue 6
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Articles  |   May 1994
Pathways signaling the regulatory volume decrease of cultured nonpigmented ciliary epithelial cells.
Author Affiliations
  • M M Civan
    Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia 19104-6085.
  • M Coca-Prados
    Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia 19104-6085.
  • K Peterson-Yantorno
    Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia 19104-6085.
Investigative Ophthalmology & Visual Science May 1994, Vol.35, 2876-2886. doi:
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    • Get Citation

      M M Civan, M Coca-Prados, K Peterson-Yantorno; Pathways signaling the regulatory volume decrease of cultured nonpigmented ciliary epithelial cells.. Invest. Ophthalmol. Vis. Sci. 1994;35(6):2876-2886.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

PURPOSE: The authors identify the signaling pathways for the regulatory volume decrease (RVD) of nonpigmented ciliary epithelial (NPE) cells. The RVD is a regulatory response triggered by swelling and reflecting KCl release by NPE cells. METHODS: The cell volumes of human nonpigmented ciliary epithelial cells were measured in suspension by electronic cell sorting. Measurements were conducted in test solutions of constant ionic strength, but osmolality was varied by sucrose. RESULTS: Cyclic AMP (cAMP), forskolin, PGE2, the PKC-inhibitor staurosporine, and increasing cytoplasmic Ca2+ activity with thapsigargin all enhanced the RVD. Leukotrienes A4, D4, E4, and the protein phosphatase inhibitor okadaic acid had no detectable effect under the current experimental conditions. The cyclooxygenase inhibitor indomethacin, the epoxygenase inhibitors ketoconazole and SKF 525A, and the PKC activator DiC8 all downregulated the RVD. The addition of the cation ionophore, gramicidin, increased the RVD. In the presence of gramicidin, cAMP, PGE2, and indomethacin did not affect the RVD, but ketoconazole, DiC8, and the calcium-calmodulin blocker trifluoroperazine still inhibited--and staurosporine still enhanced--the RVD. Many of these observations are strikingly different from results reported with other cells. Anisosmotic swelling did not increase intracellular cAMP concentration. CONCLUSIONS: The pathways signaling the regulatory responses to swelling are unique for each cell type. The authors propose that hypotonic swelling of NPE cells stimulates arachidonic acid turnover, triggering PGE2-mediated upregulation of K+ channels and epoxide-mediated upregulation of Cl- channels. Swelling may also reduce endogenous PKC activity, further upregulating Cl- channels. Calcium-calmodulin plays a permissive role in upregulating the Cl- channels.

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