A distinct membrane current in rat lens fiber cells isolated under calcium-free conditions.

PURPOSE To investigate whether lens fiber cells isolated and maintained under calcium-free conditions exhibit distinct membrane currents. METHODS Fiber cells were isolated from the cortical portion of neonate rat lenses using a trypsin digestion protocol and were maintained in EDTA-buffered Ringer's solutions. Membrane currents were recorded from fiber bundles using the whole-cell patch-clamp technique. RESULTS Cortical fiber cells of up to 600-microm length were viable and amenable to whole-cell patch-clamp recording. The major current recorded under these conditions was a slowly activating, voltage-dependent current that was markedly increased on membrane depolarization. This current appeared to be fiber cell specific and had similar properties to currents elicited by gap junction hemichannels previously recorded by others in Xenopus oocytes. CONCLUSIONS This is the first report of whole-cell patch-clamp recordings from intact elongated fiber cells. Fiber cells kept in calcium-free bath medium appear to be electrically "leaky" and exhibit a distinct membrane current that has not been described previously for lens cells. This current is unlikely to be active in the normal lens but may play a role in the depolarized cataractogenic lens.

[1]  S. Srivastava,et al.  Calcium homeostasis of isolated single cortical fibers of rat lens. , 1997, Investigative ophthalmology & visual science.

[2]  F. Bettelheim,et al.  Role of small GTP-binding proteins in lovastatin-induced cataracts. , 1997, Investigative ophthalmology & visual science.

[3]  S. Srivastava,et al.  Contribution of osmotic changes to disintegrative globulization of single cortical fibers isolated from rat lens. , 1997, Experimental eye research.

[4]  S. Srivastava,et al.  Alterations in the light transmission through single lens fibers during calcium-mediated disintegrative globulization. , 1997, Investigative ophthalmology & visual science.

[5]  R. Mathias,et al.  Physiological properties of the normal lens. , 1997, Physiological reviews.

[6]  J. H. Park,et al.  Phylogenetic Characterization of the MIP Family of Transmembrane Channel Proteins , 1996, The Journal of Membrane Biology.

[7]  C. Green,et al.  Liquefaction of cortical tissue in diabetic and galactosemic rat lenses defined by confocal laser scanning microscopy. , 1996, Investigative ophthalmology & visual science.

[8]  S. Srivastava,et al.  Mechanism of calcium-induced disintegrative globulization of rat lens fiber cells. , 1996, Investigative ophthalmology & visual science.

[9]  D. Goodenough,et al.  Heteromeric connexons in lens gap junction channels. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[10]  S. Srivastava,et al.  Calcium-mediated disintegrative globulization of isolated ocular lens fibers mimics cataractogenesis. , 1995, Experimental eye research.

[11]  C. Green,et al.  Changes in lens connexin expression lead to increased gap junctional voltage dependence and conductance. , 1995, The American journal of physiology.

[12]  C. Kushmerick,et al.  Ion, water and neutral solute transport in Xenopus oocytes expressing frog lens MIP. , 1995, Experimental eye research.

[13]  E. Beyer,et al.  Distinct behavior of connexin56 and connexin46 gap junctional channels can be predicted from the behavior of their hemi-gap-junctional channels. , 1995, Biophysical journal.

[14]  G. Chandrasekher,et al.  Calcium activated proteolysis and protein modification in the U18666A cataract. , 1993, Experimental eye research.

[15]  L. Ebihara,et al.  Properties of a nonjunctional current expressed from a rat connexin46 cDNA in Xenopus oocytes , 1993, The Journal of general physiology.

[16]  R. Bruzzone,et al.  Mouse Cx50, a functional member of the connexin family of gap junction proteins, is the lens fiber protein MP70. , 1992, Molecular biology of the cell.

[17]  D. Paul,et al.  Connexin46, a novel lens gap junction protein, induces voltage-gated currents in nonjunctional plasma membrane of Xenopus oocytes , 1991, The Journal of cell biology.

[18]  G. Zampighi,et al.  Properties of channels reconstituted from the major intrinsic protein of lens fiber membranes , 1990, The Journal of general physiology.

[19]  R. Eisenberg,et al.  Ionic channels in ocular epithelia. , 1988, Ion channels.

[20]  J L Rae,et al.  Electrical properties of structural components of the crystalline lens. , 1979, Biophysical journal.