ClC-3 is a fundamental molecular component of volume-sensitive outwardly rectifying Cl<SUP>-</SUP> channels and volume regulation in HeLa cells and <i>Xenopus laevis</i> oocytes
dc.contributor.author | Hermoso, M | |
dc.contributor.author | Satterwhite, CM | |
dc.contributor.author | Andrade, YN | |
dc.contributor.author | Hidalgo, J | |
dc.contributor.author | Wilson, SM | |
dc.contributor.author | Horowitz, B | |
dc.contributor.author | Hume, JR | |
dc.date.accessioned | 2025-01-21T01:10:28Z | |
dc.date.available | 2025-01-21T01:10:28Z | |
dc.date.issued | 2002 | |
dc.description.abstract | Volume-sensitive osmolyte and anion channels (VSOACs) are activated upon cell swelling in most vertebrate cells. Native VSOACs are believed to be a major pathway for regulatory volume decrease (RVD) through efflux of chloride and organic osmolytes. ClC-3 has been proposed to encode native VSOACs in Xenopus laevis oocytes and in some mammalian cells, including cardiac and vascular smooth muscle cells. The relationship between the ClC-3 chloride channel, the native volume-sensitive osmolyte and anion channel (VSOAC) currents, and cell volume regulation in HeLa cells and X. laevis oocytes was investigated using ClC-3 antisense. In situ hybridization in HeLa cells, semiquantitative and real-time PCR, and immunoblot studies in HeLa cells and X. laevis oocytes demonstrated the presence of ClC-3 mRNA and protein, respectively. Exposing both cell types to hypotonic solutions induced cell swelling and activated native VSOACs. Transient transfection of HeLa cells with ClC-3 antisense oligonucleotide or X. laevis oocytes injected with antisense cRNA abolished the native ClC-3 mRNA transcript and protein and significantly reduced the density of native VSOACs activated by hypotonically induced cell swelling. In addition, antisense against native ClC-3 significantly impaired the ability of HeLa cells and X. laevis oocytes to regulate their volume. These results suggest that ClC-3 is an important molecular component underlying VSOACs and the RVD process in HeLa cells and X. laevis oocytes. | |
dc.description.funder | NCRR NIH HHS | |
dc.fuente.origen | WOS | |
dc.identifier.doi | 10.1074/jbc.M205132200 | |
dc.identifier.eissn | 1083-351X | |
dc.identifier.issn | 0021-9258 | |
dc.identifier.uri | https://doi.org/10.1074/jbc.M205132200 | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/96687 | |
dc.identifier.wosid | WOS:000178662500127 | |
dc.issue.numero | 42 | |
dc.language.iso | en | |
dc.pagina.final | 40074 | |
dc.pagina.inicio | 40066 | |
dc.revista | Journal of biological chemistry | |
dc.rights | acceso restringido | |
dc.subject.ods | 03 Good Health and Well-being | |
dc.subject.odspa | 03 Salud y bienestar | |
dc.title | ClC-3 is a fundamental molecular component of volume-sensitive outwardly rectifying Cl<SUP>-</SUP> channels and volume regulation in HeLa cells and <i>Xenopus laevis</i> oocytes | |
dc.type | artículo | |
dc.volumen | 277 | |
sipa.index | WOS | |
sipa.trazabilidad | WOS;2025-01-12 |