Cellular Volume Homeostasis Kevin Strange, Ph.D. Vanderbilt University School of Medicine.

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Presentation transcript:

Cellular Volume Homeostasis Kevin Strange, Ph.D. Vanderbilt University School of Medicine

Introduction 1.How cell volume is perturbed 2.Physiological and pathophysiological consequences of cell volume change 3.Cell volume regulation: recovery from swelling and shrinkage 4.Organic osmolyte homeostasis 5.Detection of cell volume changes 6.Detection and repair of osmotic stress-induced damage

Osmotic water flow across a “semipermeable” membrane Water flows from an area of high water activity to one of lower activity Osmotic pressure, , is pressure required to stop water flow van’t Hoff relationships:  1 =RT[S] 1 ;  2 =RT[S] 2 ;  =RT  [S]

Water is in thermodynamic equilibrium across cell membranes  cell =  out solute Anisosmotic volume change: induced by extracellular osmotic perturbations Isosmotic volume change: induced by changes in cytoplasmic solute content

Physiology and pathophysiology of cell volume change Physiology: all cells are exposed to isosmotic volume perturbations Physiology: organisms and cells that live in osmotically unstable environments Pathophysiology: e.g., systemic osmolality disturbances, anoxia and ischemia, reperfusion injury, diabetes, sickle cell crisis >intertidal zone >gut >kidney

Cell volume is regulated by the gain and loss of osmotically active solutes normal volume Regulatory Volume Increase (RVI) Regulatory Volume Decrease (RVD) solute gainsolute loss

Volume regulatory electrolyte gain and loss are mediated by rapid changes in membrane transport Advantages: allows cell to rapidly correct their volume by activating pre-existing transport pathways Disadvantages: disruption of intracellular ion concentrations and cytoplasmic ionic strength

Organic osmolytes allow cells to maintain long-term stability of cytoplasmic ionic strength Amino acids AlanineProlineTaurine Polyols GlycerolSorbitolmyo-Inositol Methylamines TMAOBetaineGPC Three major classes of organic osmolytes:

Organic osmolytes are “compatible” or “non-perturbing” solutes Compatible solutes are an ubiquitous solution to osmotic stress; used by all organisms for cellular osmoregulation High water solubility: accumulated to cytoplasmic concentrations of 10s to 100s of millimolar Compatible solutes do not perturb macromolecular structure or function when present at high concentrations

Perturbing soluteCompatible solute Compatible solutes are excluded from the surface of macromolecules No net charge at physiological pH Lack strongly hydrophobic regions Steric properties

Organic osmolyte accumulation occurs by changes in synthesis or membrane transport Metabolically expensive: organic osmolytes are accumulated against concentration gradients of up to fold

Organic osmolyte accumulation requires increased gene expression Slow: requires many hours of exposure to osmotic stress

Organic osmolyte loss is mediated by: 1.Decreases in gene expression: rapid and slow components 2.Increase in passive efflux: rapid

How do cells detect volume changes? Sensor Transducer Effector Signals: mechanical stress; dilution and concentration of cytoplasmic constituents Signal transduction: kinases and phosphatases

Mechanical stress (bilayer model): force transduction via the lipid bilayer From Sukharev et al. Ann. Rev. Physiol. 59: , 1997 MscL channel swelling/stretch-activated cloned protein activated by bilayer stretch Model channels alamethicin gramicidin Membrane-bound enzymes PLA 2 GTPases E. coli MscL channel ProP transporter shrinkage-activated cloned protein activated by liposome shrinkage

Mechanical stress (tethered model): force transduction via cytoskeletal/extracellular proteins Chalfie, Driscoll and coworkers

Cytoplasmic dilution/concentration of small solutes Intracellular ionic strength Specific ions (e.g., K + ) Other solutes??

Increased cell ionic strength increases expression of organic osmolyte transporters and synthesis enzymes Aldose reductase activity Cell Na + K (mM) Uchida et al., Am. J. Physiol. 256:C614-C620, 1989

The transcriptional activator TonEBP regulates hypertonicity-induced gene expression IsotonicHypertonic TonEBP siRNA TonEBP siRNA Control Aldose reductase Na/myo-inositol cotransporter Young et al., J. Am. Soc. Nephrol. 14: , 2003

HypotonicIsotonicHypertonic Lee et al., Biochem. Biophys. Res. Comm. 294: , 2002 TonEBP translocates into the cell nucleus in response to hypertonic stress

Regulation of gene expression by TonEBP IsotonicHypertonic

Cytoplasmic dilution/concentration: macromolecular crowding and confinement Crowding and confinement alter macromolecule thermodynamic activity, structure and interactions Small changes in crowding and confinement can lead to large changes in the activity of signaling pathways, gene transcription, channel/transporter activity, etc.

Signal transduction: the case for kinases and phosphatases Swelling-activated RVD Shrinkage-activated RVI

STE20-related kinases interact with N-termini of KCl and NaK2Cl cotransporters Piechotta et al., J. Biol. Chem. 277:50812–50819, 2002 fray gene product CePASK OSR1 PASK Dan et al., Trends Cell Biol., 2001

PASK regulates shrinkage-induced activation of the NaK2Cl cotransporter Dowd and Forbush, J. Biol. Chem. 278: , 2003 Time (min) Rubidium influx PASK Kinase dead PASK Empty vector

Basal current 250 ms 1000 pA Swelling- or meiotic maturation-induced current NMDG-Cl CeGLC-7  /  CePASK CLH-3b Active P CLH-3b Inactive Meiotic maturation, swelling Meiotic arrest, shrinkage CePASK regulates the C. elegans volume-sensitive ClC channel CLH-3b Denton, Rutledge, Nehrke, Strange

Osmosensing in yeast

Some consilience (finally) Yeast STE20: shrinkage-induced activation of glycerol accumulation and RVI (turgor regulation) CePASK: shrinkage-induced inactivation of ClC anion channel PASK: shrinkage-induced activation of NaK2Cl cotransporter and RVI

How cell volume is perturbed matters Extent of volume change Rate of volume change Mechanism of volume change (anisosmotic vs. isosmotic) Cells sense:

Volume recovery Rapid electrolyte accumulation/loss Damage detection/repair Detection Cell cycle arrest Repair or apoptosis Organic osmolyte homeostasis Slow accumulation Rapid efflux/loss The cellular osmotic stress response