Loading…

Functional coupling in bovine ciliary epithelial cells is modulated by carbachol

Physiology Unit, University of Wales, Cardiff CF1 3US, United Kingdom The functional coupling of the ciliary epithelium was studied in isolated pairs (couplets) of pigmented ciliary epithelial (PCE) and nonpigmented ciliary epithelial (NPCE) cells using the whole cell patch clamp and the fluorescent...

Full description

Saved in:
Bibliographic Details
Published in:American Journal of Physiology: Cell Physiology 1997-12, Vol.273 (6), p.C1876-C1881
Main Authors: Stelling, J. W, Jacob, T. J. C
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Physiology Unit, University of Wales, Cardiff CF1 3US, United Kingdom The functional coupling of the ciliary epithelium was studied in isolated pairs (couplets) of pigmented ciliary epithelial (PCE) and nonpigmented ciliary epithelial (NPCE) cells using the whole cell patch clamp and the fluorescent dye lucifer yellow. One cell of the pair (usually the NPCE cell of a NPCE-PCE cell couplet) was accessed with a 2-5 M electrode, containing 1-2 mM lucifer yellow, in the whole cell configuration of the patch clamp. After voltage-clamp experiments were completed, cells were viewed under a fluorescent microscope to confirm that the cells were coupled. The electrical coupling of the cells was also studied by calculating the capacitance (using the time-domain technique), assuming a "supercell" model for coupled cells. The mean capacitance of coupled pairs was 79.8 ± 4.3 (SE) pF ( n  = 47) compared with single cell capacitances of 36.8 ± 3.4 pF ( n  = 10) for PCE cells and 38.1 ± 3.1 pF ( n  = 15) for NPCE cells. Octanol, carbachol (CCh), and raised extracellular Ca 2+ concentration ([Ca 2+ ] o ) all caused uncoupling in pairs (couplets) of coupled NPCE and PCE cells. At room temperature (22-24°C), the capacitance of the couplets decreased from 70.5 ± 8.0 to 48.0 ± 5.2 pF ( n = 5) when exposed to octanol (1 mM), from 73.8 ± 9.2 to 43.2 ± 9.5 pF ( n  = 4) when exposed to CCh (100 µM), and from 80.5 ± 6.7 to 49.9 ± 7.8 pF ( n  = 4) when exposed to 10 mM [Ca 2+ ] o . The response to CCh was dose dependent; at higher temperatures of 34-37°C, 10 µM CCh caused a 38% reduction in capacitance, from 53.7 ± 9.7 to 33.5 ± 3.3 pF ( n  = 7) with a half-time of 249 s, and 100 µM CCh caused a 49% reduction in capacitance, from 51.3 ± 5.6 to 26.0 ± 2.4 pF ( n  = 7) with a half-time of 124 s. After pairs uncoupled and the uncoupling agent was washed out, the cell pairs often exhibited an increase in capacitance that we interpreted as "recoupling" or a reopening of the gap junctional communication pathway; the half-time for this process was 729 s after uncoupling with 100 µM CCh and 211 s after uncoupling with 10 µM CCh. This interpretation was confirmed optically by the spread of lucifer yellow into both cells of an uncoupled pair with a time course corresponding to the increase in electrical coupling. The controllable coupling of ciliary epithelial cells extends the idea of a functional syncytium involved in active transport. PCE cells take up solute and water from the blood, which
ISSN:0363-6143
1522-1563
DOI:10.1152/ajpcell.1997.273.6.c1876