Regulation of cell volume in health and disease.

Maintenance of a constant volume in the face of extracellular and intracellular osmotic perturbations is a critical problem faced by all cells. Most cells respond to swelling or shrinkage by activating specific metabolic or membrane-transport processes that return cell volume to its normal resting state. These processes are essential for the normal function and survival of cells. This article will outline the cellular and molecular events underlying cell-volume homeostasis and discuss their relevance to medical practice. Fundamentals of Cell-Volume Regulation Meeting Osmotic Challenges Water is in thermodynamic equilibrium across the plasma membrane. In other words, the osmotic concentrations of cytoplasmic . . .

[1]  D. Benos,et al.  Activation of Amiloride‐Sensitive Sodium Transport in C6 Glioma Cells , 1984, Journal of neurochemistry.

[2]  R. Panet Serum-induced net K+ influx performed by the diuretic-sensitive transport system in quiescent NIH 3T3 mouse fibroblasts. , 1985, Biochimica et biophysica acta.

[3]  F. Giblin,et al.  Study of the polyol pathway and cell permeability changes in human lens and retinal pigment epithelium in tissue culture. , 1992, Investigative ophthalmology & visual science.

[4]  C. Joiner,et al.  Cation transport and volume regulation in sickle red blood cells. , 1993, The American journal of physiology.

[5]  R. Morrison,et al.  Volume regulation during recovery from chronic hypertonicity in brain glial cells. , 1992, The American journal of physiology.

[6]  A. Artru,et al.  Effect of mannitol on cerebrospinal fluid dynamics and brain tissue edema. , 1994, Anesthesia and analgesia.

[7]  C. Patlak,et al.  Regulation of Brain Volume Under Isosmotic and Anisosmotic Conditions , 1991 .

[8]  Lewis H. Weed,et al.  EXPERIMENTAL ALTERATION OF BRAIN BULK , 1919 .

[9]  D. Greene,et al.  Aldose reductase gene expression and osmotic dysregulation in cultured human retinal pigment epithelial cells. , 1993, The American journal of physiology.

[10]  M. Burg,et al.  Renal medullary organic osmolytes. , 1991, Physiological reviews.

[11]  J. Parker,et al.  Activation of ion transport pathways by changes in cell volume. , 1991, Biochimica et biophysica acta.

[12]  H. Grunicke,et al.  Stimulation of K+ transport systems by Ha-ras. , 1991, The Journal of biological chemistry.

[13]  K. Strange,et al.  Osmoregulation of Na(+)-inositol cotransporter activity and mRNA levels in brain glial cells. , 1992, The American journal of physiology.

[14]  R. Morrison,et al.  Osmoregulatory changes in Myo‐inositol content and Na+/Myo‐inositol contransport in rat cortical astrocytes , 1994, Glia.

[15]  Characterization and purification of a mammalian osmoregulatory protein, aldose reductase, induced in renal medullary cells by high extracellular NaCl. , 1987, The Journal of biological chemistry.

[16]  D. Becker,et al.  Effect of mannitol on ICP and CBF and correlation with pressure autoregulation in severely head-injured patients. , 1984, Journal of neurosurgery.

[17]  S. Alper,et al.  Treatment with oral clotrimazole blocks Ca(2+)-activated K+ transport and reverses erythrocyte dehydration in transgenic SAD mice. A model for therapy of sickle cell disease. , 1994, The Journal of clinical investigation.

[18]  A. V. Wolf,et al.  Osmotic volumes of distribution; idiogenic changes in osmotic pressure associated with administration of hypertonic solutions. , 1955, The American journal of physiology.

[19]  J. Grantham,et al.  Isovolumetric regulation of isolated S2 proximal tubules in anisotonic media. , 1986, The Journal of clinical investigation.

[20]  William A. Eaton,et al.  Editorial: Delay time of gelation: a possible determinant of clinical severity in sickle cell disease , 1976 .

[21]  D. Greene,et al.  Role of sorbitol accumulation and myo-inositol depletion in paranodal swelling of large myelinated nerve fibers in the insulin-deficient spontaneously diabetic bio-breeding rat. Reversal by insulin replacement, an aldose reductase inhibitor, and myo-inositol. , 1987, The Journal of clinical investigation.

[22]  S Grinstein,et al.  Na+/H+ exchange and growth factor-induced cytosolic pH changes. Role in cellular proliferation. , 1989, Biochimica et biophysica acta.

[23]  B. Ross,et al.  Brief report: organic osmolytes in the brain of an infant with hypernatremia. , 1994, The New England journal of medicine.

[24]  S. Alper,et al.  Inhibition of Ca(2+)-dependent K+ transport and cell dehydration in sickle erythrocytes by clotrimazole and other imidazole derivatives. , 1993, The Journal of clinical investigation.

[25]  K. Strange,et al.  Acute Volume Regulation of Brain Cells in Response to Hypertonic Challenge , 1993, Anesthesiology.

[26]  D. Becker,et al.  Mannitol causes compensatory cerebral vasoconstriction and vasodilation in response to blood viscosity changes. , 1983, Journal of neurosurgery.

[27]  R. Balaban,et al.  Induction of aldose reductase and sorbitol in renal inner medullary cells by elevated extracellular NaCl. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[28]  H. Tallan,et al.  Taurine: biological update. , 1986, Annual review of biochemistry.

[29]  K. Strange,et al.  Regulation of solute and water balance and cell volume in the central nervous system. , 1992, Journal of the American Society of Nephrology : JASN.

[30]  D. Greene,et al.  Sorbitol, phosphoinositides, and sodium-potassium-ATPase in the pathogenesis of diabetic complications. , 1987, The New England journal of medicine.

[31]  J. Parker In defense of cell volume? , 1993, The American journal of physiology.

[32]  E. Feldman,et al.  Aldose reductase inhibitors: an approach to the treatment of diabetic nerve damage. , 1993, Diabetes/metabolism reviews.

[33]  L. H. Weed,et al.  PRESSURE CHANGES IN THE CEREBRO-SPINAL FLUID FOLLOWING INTRAVENOUS INJECTION OF SOLUTIONS OF VARIOUS CONCENTRATIONS , 1919 .

[34]  M. Canessa,et al.  Deoxygenation inhibits the volume-stimulated, Cl(-)-dependent K+ efflux in SS and young AA cells: a cytosolic Mg2+ modulation. , 1987, Blood.

[35]  M. Burg,et al.  Sorbitol, osmoregulation, and the complications of diabetes. , 1988, The Journal of clinical investigation.

[36]  D. Greene,et al.  Altered aldose reductase gene regulation in cultured human retinal pigment epithelial cells. , 1993, The Journal of clinical investigation.

[37]  Lew Vl,et al.  Activation of calcium-dependent potassium channels in deoxygenated sickled red cells. , 1987 .

[38]  E. Feldman,et al.  Complications: Neuropathy, Pathogenetic Considerations , 1992, Diabetes Care.

[39]  C. Nicholson,et al.  Extracellular volume decreases while cell volume is maintained by ion uptake in rat brain during acute hypernatremia. , 1991, The Journal of physiology.

[40]  M. Canessa Red cell volume-related ion transport systems in hemoglobinopathies. , 1991, Hematology/oncology clinics of North America.

[41]  F. Diecke,et al.  Myo-inositol transport in the lens of galactose-maintained rats. , 1992, Current eye research.

[42]  K. Strange Are All Cell Volume Changes the Same , 1994 .

[43]  F. Giblin,et al.  Polyol accumulation in cultured human lens epithelial cells. , 1991, Experimental Eye Research.