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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...
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Published in: | American Journal of Physiology: Cell Physiology 1997-12, Vol.273 (6), p.C1876-C1881 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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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 |
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ISSN: | 0363-6143 1522-1563 |
DOI: | 10.1152/ajpcell.1997.273.6.c1876 |