Astrocyte swelling leads to membrane unfolding, not membrane insertion

The mechanisms mediating the release of chemical transmitters from astrocytes are the subject of intense research. Recent experiments have shown that hypotonic conditions stimulate the release of glutamate and ATP from astrocytes, but a mechanistic understanding of this process is not available. To determine whether hypotonicity activates the process of regulated exocytosis, we monitored membrane capacitance by the whole‐cell patch‐clamp technique whilst a hypotonic medium was applied to cultured astrocytes. If exocytosis is triggered under hypotonic conditions, as it is following increases in cytosolic calcium, a net increase in membrane surface area, monitored by measuring the whole‐cell membrane capacitance, is expected. Simultaneous measurements of cell size and whole‐cell membrane conductance and surface area demonstrated that hypotonic medium (210 mOsm for 200 s) resulted in an increase in membrane conductance and in the swelling of cultured astrocytes by an average of 40%, as monitored by cell cross‐sectional area, but without any corresponding change in membrane surface area. As we have demonstrated that capacitance measurements have the sensitivity to detect increases in cell surface area as small as 0.5%, we conclude that cell swelling occurs via an exocytosis‐independent mechanism, probably involving the unfolding of the plasma membrane.

[1]  H. Kimelberg,et al.  [3H]taurine and D-[3H]aspartate release from astrocyte cultures are differently regulated by tyrosine kinases. , 1999, The American journal of physiology.

[2]  P. Haydon,et al.  Defining pathways of loss and secretion of chemical messengers from astrocytes , 2004, Glia.

[3]  F. Alvarez-Leefmans,et al.  Regulatory Volume Decrease and Intracellular Ca2+ in Murine Neuroblastoma Cells Studied with Fluorescent Probes , 1998, The Journal of general physiology.

[4]  P. Haydon,et al.  Imaging Extracellular Waves of Glutamate during Calcium Signaling in Cultured Astrocytes , 2000, The Journal of Neuroscience.

[5]  S. White The Physical Nature of Planar Bilayer Membranes , 1986 .

[6]  S. Lidofsky,et al.  Autocrine signaling through ATP release represents a novel mechanism for cell volume regulation. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[7]  H. Kimelberg,et al.  ATP potently modulates anion channel-mediated excitatory amino acid release from cultured astrocytes. , 2002, American journal of physiology. Cell physiology.

[8]  G. Kilic,et al.  Vesicular exocytosis contributes to volume-sensitive ATP release in biliary cells. , 2004, American journal of physiology. Gastrointestinal and liver physiology.

[9]  L. Vaca,et al.  Osmotic Swelling‐Induced Changes in Cytosolic Calcium Do Not Affect Regulatory Volume Decrease in Rat Cultured Suspended Cerebellar Astrocytes , 1998, Journal of neurochemistry.

[10]  R. Zorec,et al.  Osmotic swelling of hepatocytes increases membrane conductance but not membrane capacitance. , 1995, Biophysical journal.

[11]  J. Schwarts,et al.  Preparation and characterization of type 1 astrocytes cultured from adult rat cortex, cerebellum, and striatum , 1992, Glia.

[12]  Fang Liu,et al.  Glutamate-mediated astrocyte–neuron signalling , 1994, Nature.

[13]  N. McCarty,et al.  Calcium signaling in cell volume regulation. , 1992, Physiological reviews.

[14]  E. Hansson Metabotropic glutamate receptor activation induces astroglial swelling. , 1994, The Journal of biological chemistry.

[15]  M. Matteoli,et al.  Storage and Release of ATP from Astrocytes in Culture* , 2003, The Journal of Biological Chemistry.

[16]  A. Houtsmuller,et al.  Increased Vesicle Recycling in Response to Osmotic Cell Swelling , 2003, Journal of Biological Chemistry.

[17]  D. Attwell,et al.  Modulation of extracellular glutamate concentration in rat brain slices by cystine‐glutamate exchange , 1999, The Journal of physiology.

[18]  E. Newman New roles for astrocytes: Regulation of synaptic transmission , 2003, Trends in Neurosciences.

[19]  F. Kirchhoff,et al.  Segregated Expression of AMPA-Type Glutamate Receptors and Glutamate Transporters Defines Distinct Astrocyte Populations in the Mouse Hippocampus , 2003, The Journal of Neuroscience.

[20]  Alessandra Fabbro,et al.  Quantal release of ATP from clusters of PC12 cells , 2004, The Journal of physiology.

[21]  Gordan Kilic Exocytosis in bovine chromaffin cells: studies with patch-clamp capacitance and FM1-43 fluorescence. , 2002, Biophysical journal.

[22]  Maja Potokar,et al.  Properties of Ca2+‐dependent exocytosis in cultured astrocytes , 2004, Glia.

[23]  R. Tsien,et al.  A new generation of Ca2+ indicators with greatly improved fluorescence properties. , 1985, The Journal of biological chemistry.

[24]  H. Kimelberg,et al.  Role of calcium in astrocyte volume regulation and in the release of ions and amino acids , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[25]  J. Olson,et al.  Increased potassium, chloride, and taurine conductances in astrocytes during hypoosmotic swelling , 1997, Glia.

[26]  J. Meldolesi,et al.  Astrocytes, from brain glue to communication elements: the revolution continues , 2005, Nature Reviews Neuroscience.

[27]  B. Ransom,et al.  Functional Hemichannels in Astrocytes: A Novel Mechanism of Glutamate Release , 2003, The Journal of Neuroscience.

[28]  Denise Feighan,et al.  ATP released from astrocytes during swelling activates chloride channels. , 2003, Journal of neurophysiology.

[29]  T. Takano,et al.  Receptor-mediated glutamate release from volume sensitive channels in astrocytes. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[30]  D. Attwell,et al.  Non-vesicular release of glutamate from glial cells by reversed electrogenic glutamate uptake , 1990, Nature.

[31]  Manfred Lindau,et al.  Patch-clamp techniques for time-resolved capacitance measurements in single cells , 1988, Pflügers Archiv.

[32]  M. Oike,et al.  Involvement of Rho‐kinase and tyrosine kinase in hypotonic stress‐induced ATP release in bovine aortic endothelial cells , 2001, The Journal of physiology.

[33]  Y. Okada,et al.  Exocytosis upon osmotic swelling in human epithelial cells. , 1992, Biochimica et biophysica acta.

[34]  P. Haydon Glia: listening and talking to the synapse , 2001, Nature Reviews Neuroscience.

[35]  Michael M. Halassa,et al.  Fusion-related Release of Glutamate from Astrocytes* , 2004, Journal of Biological Chemistry.

[36]  M. Salter,et al.  ATP-evoked increases in intracellular calcium in neurons and glia from the dorsal spinal cord , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[37]  M. Cahalan,et al.  Membrane chloride conductance and capacitance in Jurkat T lymphocytes during osmotic swelling. , 1994, Biophysical journal.

[38]  H. Pasantes‐Morales,et al.  Osmosensitive Release of Neurotransmitter Amino Acids: Relevance and Mechanisms , 2002, Neurochemical Research.

[39]  T. Takano,et al.  Beyond the role of glutamate as a neurotransmitter , 2002, Nature Reviews Neuroscience.

[40]  Robert Zorec,et al.  13 - Electrophysiological Study of Hormone Secretion by Single Adenohypophyseal Cells , 1991 .

[41]  U. Kubitscheck,et al.  Osmotically evoked shrinking of guard-cell protoplasts causes vesicular retrieval of plasma membrane into the cytoplasm , 2000, Planta.

[42]  H. Kimelberg,et al.  [3H]taurine andd-[3H]aspartate release from astrocyte cultures are differently regulated by tyrosine kinases. , 1999, American journal of physiology. Cell physiology.

[43]  R. North,et al.  Brilliant blue G selectively blocks ATP-gated rat P2X(7) receptors. , 2000, Molecular pharmacology.

[44]  D. Attwell,et al.  Glutamate release in severe brain ischaemia is mainly by reversed uptake , 2000, Nature.

[45]  R. Kinne,et al.  Cell volume regulation: osmolytes, osmolyte transport, and signal transduction. , 2003, Reviews of physiology, biochemistry and pharmacology.

[46]  INTERNATIONAL SOCIETY FOR NEUROCHEMISTRY , 1976 .

[47]  E Neher,et al.  Discrete changes of cell membrane capacitance observed under conditions of enhanced secretion in bovine adrenal chromaffin cells. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[48]  M. Kreft,et al.  Vesicle mobility studied in cultured astrocytes. , 2005, Biochemical and biophysical research communications.

[49]  S. Duan,et al.  P2X7 Receptor-Mediated Release of Excitatory Amino Acids from Astrocytes , 2003, The Journal of Neuroscience.

[50]  S. Jeftinija,et al.  ATP stimulates calcium‐dependent glutamate release from cultured astrocytes , 2001, Journal of neurochemistry.