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 The role of the membrane potential in chondrocyte volume regulation Lewis R; Asplin KE; Bruce G; Dart C; Mobasheri A; Barrett-Jolley RJ Cell Physiol  2011[Nov]; 226 (11): 2979-86Many cell types have significant negative resting membrane potentials (RMPs)  resulting from the activity of potassium-selective and chloride-selective ion  channels. In excitable cells, such as neurones, rapid changes in membrane  permeability underlie the generation of action potentials. Chondrocytes have less  negative RMPs and the role of the RMP is not clear. Here we examine the basis of  the chondrocyte RMP and possible physiological benefits. We demonstrate that  maintenance of the chondrocyte RMP involves gadolinium-sensitive cation channels.  Pharmacological inhibition of these channels causes the RMP to become more  negative (100 microM gadolinium: DeltaV(m)  = -30 +/- 4 mV). Analysis of the  gadolinium-sensitive conductance reveals a high permeability to calcium ions  (PCa/PNa  approximately 80) with little selectivity between monovalent ions; similar to that  reported elsewhere for TRPV5. Detection of TRPV5 by PCR and immunohistochemistry  and the sensitivity of the RMP to the TRPV5 inhibitor econazole (DeltaV(m)   = -18 +/- 3 mV) suggests that the RMP may be, in part, controlled by TRPV5. We  investigated the physiological advantage of the relatively positive RMP using a  mathematical model in which membrane stretch activates potassium channels  allowing potassium efflux to oppose osmotic water uptake. At very negative RMP  potassium efflux is negligible, but at more positive RMP it is sufficient to  limit volume increase. In support of our model, cells clamped at -80 mV and  challenged with a reduced osmotic potential swelled approximately twice as much  as cells at +10 mV. The positive RMP may be a protective adaptation that allows  chondrocytes to respond to the dramatic osmotic changes, with minimal changes in  cell volume.|Animals[MESH]|Calcium/physiology[MESH]|Cattle[MESH]|Cell Size[MESH]|Cells, Cultured[MESH]|Chondrocytes/*cytology/drug effects[MESH]|Dogs[MESH]|Gadolinium/pharmacology[MESH]|Horses[MESH]|Membrane Potentials/drug effects/*physiology[MESH]|Models, Biological[MESH]|Rats[MESH]|Sheep[MESH]|TRPV Cation Channels/drug effects/physiology[MESH]
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