September 1997
Volume 38, Issue 10
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Articles  |   September 1997
Membrane-associated carbonic anhydrase in cultured rabbit nonpigmented ciliary epithelium.
Author Affiliations
  • Q Wu
    Department of Pharmacology and Toxicology, University of Louisville, Kentucky 40292, USA.
  • N A Delamere
    Department of Pharmacology and Toxicology, University of Louisville, Kentucky 40292, USA.
  • W Pierce, Jr
    Department of Pharmacology and Toxicology, University of Louisville, Kentucky 40292, USA.
Investigative Ophthalmology & Visual Science September 1997, Vol.38, 2093-2102. doi:
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    • Get Citation

      Q Wu, N A Delamere, W Pierce; Membrane-associated carbonic anhydrase in cultured rabbit nonpigmented ciliary epithelium.. Invest. Ophthalmol. Vis. Sci. 1997;38(10):2093-2102.

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

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Abstract

PURPOSE: To measure the activity of membrane-associated carbonic anhydrase (CA) in cultured rabbit nonpigmented epithelial (NPE) cells, determine its identity and its sensitivity to extracellular trypsin, and compare the ability of acetazolamide and a cell-impermeant dextran-bound CA inhibitor to change cytoplasmic pH. METHODS: Studies were conducted using a cell line derived from rabbit NPE. The cells were lysed and separated into soluble and insoluble fractions by differential centrifugation. CA activity in these fractions was determined using a CO2 hydration assay. In studies with intact cells, a membrane-impermeable high-molecular-weight dextran-bound inhibitor (DBI) was synthesized and used to selectively bind and inhibit the extracellular-facing membrane-bound CA. Measurements of CA activity in intact red blood cells were conducted to confirm DBI remains extracellular. Acetazolamide, a membrane-permeable CA inhibitor, was used to inhibit total CA activity. Intracellular pH was determined using the pH-dependent absorbance of the fluorescent dye BCECF-AM. RESULTS: A low-speed pellet enriched with plasma membrane material accounted for 22.3 +/- 6.1% (n = 18) of the total CA activity in the cultured NPE. When intact cells were exposed to trypsin-EDTA, a 28% reduction of membrane-associated CA activity was observed; DBI inhibited this CA activity loss. Cytosolic CA activity was inhibited by 0.2% sodium dodecyl sulfate (SDS). In contrast, membrane-associated CA was SDS resistant, a characteristic of the CA-IV isozyme. By Western blot, CA-IV immunoreactive polypeptide was detected in the cultured cells and also in native rabbit and porcine ciliary epithelium. Inhibition of total CA activity with acetazolamide and inhibition of extracellular-facing membrane-associated CA with DBI caused an identical intracellular pH decrease in intact NPE cells. CONCLUSIONS: Expression of the CA-IV isozyme could account for the significant fraction of CA activity in the cultured NPE, which is membrane associated and SDS resistant. Sensitivity to tryptic hydrolysis suggests the membrane-associated CA partially faces extracellularly. As judged by responses to an extracellular CA inhibitor, the membrane-associated CA has a functional role in maintaining cytoplasmic pH.

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