Literature DB >> 2410192

The application of patch clamp methods to ocular epithelia.

J L Rae.   

Abstract

The techniques of patch voltage clamping and whole cell clamping have been applied to the lenses and corneas of several species of animals. Numerous ion channels have been found in the basal and apical membranes of lens epithelial cells, anterior and posterior surface lens fibers, apical membrane of corneal endothelial cells, and apical membrane of the second layer of corneal epithelial cells. No ion channels have been found in deep lens fiber membranes to date. There are 9-11 different kinds of potassium channels in ocular epithelial membranes, several different kinds of non-selective cation channels, and one non-selective channel with a large unit conductance. Sodium selective channels are seen only rarely while chloride selective channels have not been seen at all. Several channels have not yet been identified unequivocally. Using the gigohm seal technique, it is possible to show that the frog lens epithelial cell membrane is dominated by potassium channels. Also, a technique is described for using the reversal potential of a 25-30 pS non-selective cation channel to measure the resting voltage of epithelial cells without penetrating them. The results of lens ion channel localization studies are in only qualitative agreement with previous lens channel localization studies which used whole lens impedance and ion substitution techniques. Limitations of using the patch clamp for ion channel localization are presented.

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Year:  1985        PMID: 2410192     DOI: 10.3109/02713688509025155

Source DB:  PubMed          Journal:  Curr Eye Res        ISSN: 0271-3683            Impact factor:   2.424


  17 in total

1.  Single-membrane and cell-to-cell permeability properties of dissociated embryonic chick lens cells.

Authors:  A G Miller; G A Zampighi; J E Hall
Journal:  J Membr Biol       Date:  1992-06       Impact factor: 1.843

Review 2.  Stress-induced corneal epithelial apoptosis mediated by K+ channel activation.

Authors:  Luo Lu
Journal:  Prog Retin Eye Res       Date:  2006-09-07       Impact factor: 21.198

3.  A cation channel in frog lens epithelia responsive to pressure and calcium.

Authors:  K E Cooper; J M Tang; J L Rae; R S Eisenberg
Journal:  J Membr Biol       Date:  1986       Impact factor: 1.843

4.  Potassium channels in the luminal membrane of rabbit proximal straight tubule. Evidence from vesicle studies.

Authors:  C Jacobsen; H Røigaard-Petersen; M I Sheikh
Journal:  Biochem J       Date:  1989-08-15       Impact factor: 3.857

5.  Membrane and junctional properties of dissociated frog lens epithelial cells.

Authors:  K Cooper; J L Rae; P Gates
Journal:  J Membr Biol       Date:  1989-11       Impact factor: 1.843

6.  Potassium channel in rabbit corneal endothelium activated by external anions.

Authors:  J L Rae; J Dewey; K Cooper; P Gates
Journal:  J Membr Biol       Date:  1990-03       Impact factor: 1.843

7.  Single-channel recordings from the apical membrane of the toad urinary bladder epithelial cell.

Authors:  S Frings; R D Purves; A D Macknight
Journal:  J Membr Biol       Date:  1988-12       Impact factor: 1.843

Review 8.  Ion channel subconductance states.

Authors:  J A Fox
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

9.  Ba2+-inhibitable 86Rb+ fluxes across membranes of vesicles from toad urinary bladder.

Authors:  H Garty; M M Civan
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

10.  Membrane and junctional properties of the isolated frog lens epithelium.

Authors:  G Duncan; S Stewart; A R Prescott; R M Warn
Journal:  J Membr Biol       Date:  1988-06       Impact factor: 1.843

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