Source:http://linkedlifedata.com/resource/pubmed/id/16769051
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2006-9-4
|
pubmed:abstractText |
In the eye, trabecular meshwork (TM) cell volume may be an important determinant of aqueous humor outflow. Among their functions, ClC-2 chloride channels are thought to be involved in regulation of cellular volume and intracellular [Cl(-)]. We characterized the properties and modulation of an inwardly rectifying chloride current activated in these cells. Patch-clamp recordings revealed inwardly rectifying chloride currents activated by membrane hyperpolarization in primary cultures of both bovine (BTM) and human (HTM) TM cells. Electrophysiological properties and anion permeability sequence (Cl(-)>Br(-)>I(-)>F(-)) were in agreement with previous data for ClC-2 in other cells. The currents were blocked by Cd(2+) and enhanced by extracellular acidification, 8Br-cAMP and cell swelling, while extracellular alkalinization decreased them. RT-PCR experiments using total RNA revealed the molecular expression of ClC-2 channels. Previously we reported the involvement of swelling-activated chloride channels (Cl(swell)) and Ca(2+)-activated K(+) channels (BK(Ca)) in cell volume and outflow facility regulation. However, in the present analysis, cell volume experiments in calcein-loaded cells and outflow facility studies performed in bovine anterior segments revealed that ClC-2 channels do not make a significant contribution to the recovery of cellular volume or to the regulation of the outflow facility. Nevertheless, ClC-2 modulation by different stimuli may contribute to intracellular [Cl(-)] regulation and other cellular functions yet to be determined in the TM.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0014-4835
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
83
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
877-89
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:16769051-8-Bromo Cyclic Adenosine Monophosphate,
pubmed-meshheading:16769051-Animals,
pubmed-meshheading:16769051-Aqueous Humor,
pubmed-meshheading:16769051-Cadmium,
pubmed-meshheading:16769051-Cattle,
pubmed-meshheading:16769051-Cell Size,
pubmed-meshheading:16769051-Cells, Cultured,
pubmed-meshheading:16769051-Chloride Channels,
pubmed-meshheading:16769051-Humans,
pubmed-meshheading:16769051-Ion Channel Gating,
pubmed-meshheading:16769051-Patch-Clamp Techniques,
pubmed-meshheading:16769051-Trabecular Meshwork
|
pubmed:year |
2006
|
pubmed:articleTitle |
Identification and functional characterization of ClC-2 chloride channels in trabecular meshwork cells.
|
pubmed:affiliation |
Laboratory of Neurophysiology, Department of Physiological Sciences I-Institute of Biomedical Investigations August Pi i Sunyer, IDIBAPS, School of Medicine, University of Barcelona, Casanova 143, E-08036 Barcelona, Spain.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
|