Inward-rectifying potassium channels in retinal glial (Muller) cells

The voltage- and K(+)-dependent properties of Muller cell currents and channels were characterized in freshly dissociated salamander Muller cells. In whole-cell voltage-clamp experiments, cells with endfeet intact and cells missing endfeet both displayed strong inward rectification. The rectification was similar in shape in both groups of cells but currents were 9.2 times larger in cells with endfeet. Ba2+ at 100 microM reduced the inward current to 6.8% of control amplitude. Decreasing external K+ concentration shifted the cell current-voltage (I-V) relation in a hyperpolarizing direction and reduced current magnitude. In multichannel, cell-attached patch-clamp experiments, patches from both endfoot and soma membrane displayed strong inward rectification. Currents were 38 times larger in endfoot patches. In single-channel, cell-attached patch-clamp experiments, inward- rectifying K+ channels were, in almost all cases, the only channels present in patches of endfoot, proximal process, and soma membrane. Channel conductance was 27.8 pS in 98 mM external K+. Reducing external K+ shifted the channel reversal potential in a hyperpolarizing direction and reduced channel conductance. Channel open probability varied as a function of voltage, being reduced at more negative potentials. Together, these observations demonstrate that the principal ion channel in all Muller cell regions is an inward-rectifying K+ channel. Channel density is far higher on the cell endfoot than in other cell regions. Whole-cell I-V plots of cells bathed in 12, 7, 4, and 2.5 mM K+ were fit by an equation including Boltzmann relation terms representing channel rectification and channel open probability. This equation was incorporated into a model of K+ dynamics in the retina to evaluate the significance of inward-rectifying channels to the spatial buffering/K+ siphoning mechanism of K+ regulation. Compared with ohmic channels, inward-rectifying channels increased the rate of K+ clearance from the retina by 23% for a 1 mM K+ increase and by 137% for a 9.5 mM K+ increase, demonstrating that Muller cell inward- rectifying channels enhance K+ regulation in the retina.

[1]  B Sakmann,et al.  Conductance properties of single inwardly rectifying potassium channels in ventricular cells from guinea‐pig heart. , 1984, The Journal of physiology.

[2]  D. Corey,et al.  Ion channel expression by white matter glia: The type-1 astrocyte , 1990, Neuron.

[3]  E. Newman,et al.  Model of potassium dynamics in the central nervous system , 1988, Glia.

[4]  G. Wilson,et al.  Ion channels in axon and Schwann cell membranes at paranodes of mammalian myelinated fibers studied with patch clamp , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[5]  G. Cordingley,et al.  Responses of electrical potential, potassium levels, and oxidative metabolic activity of the cerebral neocortex of cats , 1975, Brain Research.

[6]  A. Gardner-Medwin A new framework for assessment of potassium-buffering mechanisms. , 1986, Annals of the New York Academy of Sciences.

[7]  D. Attwell,et al.  Is the potassium channel distribution in glial cells optimal for spatial buffering of potassium? , 1985, Biophysical journal.

[8]  W. Singer,et al.  Extracellular potassium gradients and visual receptive fields in the cat striate cortex , 1975, Brain Research.

[9]  E Syková,et al.  Extracellular K+ accumulation in the central nervous system. , 1983, Progress in biophysics and molecular biology.

[10]  E. Newman,et al.  Control of extracellular potassium levels by retinal glial cell K+ siphoning. , 1984, Science.

[11]  B. Barres,et al.  New roles for glia , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[12]  C. Vandenberg Inward rectification of a potassium channel in cardiac ventricular cells depends on internal magnesium ions. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[13]  R. D. do Carmo,et al.  Spreading depression of Leão probed with ion-selective microelectrodes in isolated chick retina. , 1984, Anais da Academia Brasileira de Ciencias.

[14]  D. V. van Essen,et al.  Cell structure and function in the visual cortex of the cat , 1974, The Journal of physiology.

[15]  E. Newman,et al.  Light-evoked increases in extracellular K+ in the plexiform layers of amphibian retinas , 1985, The Journal of general physiology.

[16]  A. Gardner-Medwin,et al.  Analysis of potassium dynamics in mammalian brain tissue. , 1983, The Journal of physiology.

[17]  E. Newman Distribution of potassium conductance in mammalian Muller (glial) cells: a comparative study , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[18]  G. Somjen Extracellular potassium in the mammalian central nervous system. , 1979, Annual review of physiology.

[19]  T. Brismar,et al.  Inward rectifying potassium channels in human malignant glioma cells , 1989, Brain Research.

[20]  H. Matsuda Magnesium gating of the inwardly rectifying K+ channel. , 1991, Annual review of physiology.

[21]  E. Newman Potassium conductance block by barium in amphibian Mu¨ller cells , 1989, Brain Research.

[22]  S. Chiu,et al.  Potassium channel regulation in Schwann cells during early developmental myelinogenesis , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[23]  E. Newman,et al.  Regional specialization of retinal glial cell membrane , 1984, Nature.

[24]  D P Corey,et al.  Ion channel expression by white matter glia: I. Type 2 astrocytes and oligodendrocytes , 1988, Glia.

[25]  A. Reichenbach,et al.  Spatial buffering of potassium by retinal müller (glial) cells of various morphologies calculated by a model , 1987, Neuroscience.

[26]  B. Rudy,et al.  Diversity and ubiquity of K channels , 1988, Neuroscience.

[27]  Seung U. Kim,et al.  Single channel potassium currents in cultured adult bovine oligodendrocytes , 1989, Glia.

[28]  E. Newman Membrane physiology of retinal glial (Muller) cells , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[29]  L. Proenza,et al.  Relationship between Müller cell responses, a local transretinal potential, and potassium flux. , 1977, Journal of neurophysiology.

[30]  S. W. Kuffler,et al.  Effect of nerve impulses on the membrane potential of glial cells in the central nervous system of amphibia. , 1966, Journal of neurophysiology.

[31]  B. Sakmann,et al.  Voltage‐dependent inactivation of inward‐rectifying single‐channel currents in the guinea‐pig heart cell membrane. , 1984, The Journal of physiology.

[32]  David P. Corey,et al.  Ion channel expression by white matter glia: The O-2A glial progenitor cell , 1990, Neuron.

[33]  Seung U. Kim,et al.  Existence of inward potassium currents in adult human oligodendrocytes , 1989, Neuroscience Letters.

[34]  R. Keynes The ionic channels in excitable membranes. , 1975, Ciba Foundation symposium.

[35]  W. H. Miller,et al.  Microelectrode study of spreading depression (SD) in frog retina-Müller cell activity and [K+] during SD--. , 1976, The Japanese journal of physiology.

[36]  L. Frishman,et al.  Light-evoked changes in [K+]o in proximal portion of light-adapted cat retina. , 1992, Journal of neurophysiology.

[37]  S. Hagiwara Membrane potential-dependent ion channels in cell membrane : phylogenetic and developmental approaches , 1983 .

[38]  S Miyazaki,et al.  Potassium current and the effect of cesium on this current during anomalous rectification of the egg cell membrane of a starfish , 1976, The Journal of general physiology.

[39]  A. R. Gardner A New Framework for Assessment of Potassium‐Buffering Mechanisms , 1986 .

[40]  H. Lux The Kinetics of Extracellular Potassium: Relation to Epileptogenesis1 , 1974, Epilepsia.

[41]  H. Kettenmann,et al.  Heterogeneity of potassium currents in cultured oligodendrocytes , 1988, Glia.

[42]  C. Nicholson,et al.  Calcium and potassium changes in extracellular microenvironment of cat cerebellar cortex. , 1978, Journal of neurophysiology.

[43]  N. Abbott The neuronal microenvironment , 1986, Trends in Neurosciences.

[44]  E. Newman High potassium conductance in astrocyte endfeet. , 1986, Science.

[45]  C. Karwoski,et al.  Neurons, potassium, and glia in proximal retina of Necturus , 1980, The Journal of general physiology.

[46]  D. Attwell,et al.  Endfeet of retinal glial cells have higher densities of ion channels that mediate K+ buffering , 1986, Nature.

[47]  S. W. Kuffler,et al.  Physiological properties of glial cells in the central nervous system of amphibia. , 1966, Journal of neurophysiology.

[48]  R. Miller,et al.  Extracellular K+ activity changes related to electroretinogram components. I. Amphibian (I-type) retinas , 1985, The Journal of general physiology.

[49]  U. Heinemann,et al.  Relations between slow extracellular potential changes, glial potassium buffering, and electrolyte and cellular volume changes during neuronal hyperactivity in cat brain , 1989, Glia.

[50]  E. Newman Regulation of potassium levels by glial cells in the retina , 1985, Trends in Neurosciences.

[51]  E. Newman,et al.  Spatial buffering of light-evoked potassium increases by retinal Müller (glial) cells. , 1989, Science.

[52]  P. Pennefather,et al.  The mechanism of rectification of iK1 in canine Purkinje myocytes , 1990, The Journal of general physiology.

[53]  E. Newman Voltage-dependent calcium and potassium channels in retinal glial cells , 1985, Nature.

[54]  H. Irisawa,et al.  Ohmic conductance through the inwardly rectifying K channel and blocking by internal Mg2+ , 1987, Nature.