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Regulation of the cell swelling-activated chloride conductance by cholesterol-rich membrane domains

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Abstract:

Abstract Aim: 

The role of high cholesterol-containing microdomains in the signal transduction cascade leading to the activation of volume-regulated anion channels (VRACs) was studied. Methods: 

Osmotic cell swelling-induced efflux of 125I was determined in human epithelial Intestine 407 cells and in skin fibroblasts obtained from healthy controls or Niemann–Pick type C (NPC) patients. Cellular cholesterol content was modulated by pre-incubation with 2-hydroxypropyl-β-cyclodextrin in the presence of acceptor lipid vesicles. Results: 

Osmotic cell swelling of human Intestine 407 cells leads to the rapid activation of a compensatory anion conductance. Treatment of the cells with cyclodextrin enhanced the response to submaximal hypotonic stimulation by approx. twofold, but did not further increase the efflux elicited by a saturating stimulus. In contrast, the volume-sensitive anion efflux was markedly inhibited when cholesterol-loaded cyclodextrin was used. Potentiation of the response by cholesterol depletion was maintained in caveolin-1 deficient Caco-2 colonocytes as well as in sphingomyelinase-treated Intestine 407 cells, indicating that cholesterol-rich microdomains are not crucially involved. However, treatment of the cells with progesterone, an inhibitor of NPC1-dependent endosomal cholesterol trafficking, not only markedly reduced the hypotonicity-provoked anion efflux, but also prevented its potentiation by cyclodextrin. In addition, the volume-sensitive anion efflux from human NPC skin fibroblasts was significantly smaller when compared with control fibroblasts. Conclusions: 

The results support a model of regulatory volume decrease involving recruitment of volume-sensitive anion channels from intracellular compartments to the plasma membrane.

Keywords: Niemann–Pick type C; chloride channel; cholesterol; progesterone; regulatory volume decrease

Document Type: Research Article

DOI: https://doi.org/10.1111/j.1748-1716.2006.01534.x

Affiliations: 1: Department of Biochemistry, Erasmus University Medical Center, Rotterdam, The Netherlands 2: Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands

Publication date: 2006-05-01

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