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- Publisher Website: 10.1016/S0014-5793(00)01831-7
- Scopus: eid_2-s2.0-0034725459
- PMID: 10922480
- WOS: WOS:000088644200023
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Article: Cholestan-3β,5α,6β-triol, but not 7-ketocholesterol, suppresses taurocholate-induced mucin secretion by cultured dog gallbladder epithelial cells
Title | Cholestan-3β,5α,6β-triol, but not 7-ketocholesterol, suppresses taurocholate-induced mucin secretion by cultured dog gallbladder epithelial cells |
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Authors | |
Keywords | Cholesterol Cytotoxicity Epithelial cell Gallbladder Mucin secretion Oxysterol |
Issue Date | 2000 |
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/febslet |
Citation | Febs Letters, 2000, v. 478 n. 1-2, p. 113-118 How to Cite? |
Abstract | In order to investigate oxysterol-mediated effects on the biliary system, we studied the effects of cholestan-3β,5α,6β-triol (TriolC) and 7-ketocholesterol (7KC) on gallbladder epithelial cells. We compared their cell proliferation effects in cultured dog gallbladder epithelial cells (DGBE) to their effects in cultured human pulmonary artery endothelial cells (HPAE). Oxysterols inhibited cell proliferation in a dose-dependent fashion. Oxysterols inhibited cell growth to 50% of control at a higher dose for DGBE cells than for HPAE cells. TriolC was more cytotoxic than 7KC. We also investigated the effect of oxysterols on bile salt-induced mucin secretion by DGBE cells. TriolC suppressed mucin secretion by DGBE cells, whereas 7KC did not. These findings support the hypothesis that biliary oxysterols affect gallbladder mucosal function. Copyright (C) 2000 Federation of European Biochemical Societies. |
Persistent Identifier | http://hdl.handle.net/10722/92519 |
ISSN | 2023 Impact Factor: 3.0 2023 SCImago Journal Rankings: 1.208 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Yoshida, T | en_HK |
dc.contributor.author | Klinkspoor, JH | en_HK |
dc.contributor.author | Kuver, R | en_HK |
dc.contributor.author | Wrenn, SP | en_HK |
dc.contributor.author | Kaler, EW | en_HK |
dc.contributor.author | Lee, SP | en_HK |
dc.date.accessioned | 2010-09-17T10:48:42Z | - |
dc.date.available | 2010-09-17T10:48:42Z | - |
dc.date.issued | 2000 | en_HK |
dc.identifier.citation | Febs Letters, 2000, v. 478 n. 1-2, p. 113-118 | en_HK |
dc.identifier.issn | 0014-5793 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/92519 | - |
dc.description.abstract | In order to investigate oxysterol-mediated effects on the biliary system, we studied the effects of cholestan-3β,5α,6β-triol (TriolC) and 7-ketocholesterol (7KC) on gallbladder epithelial cells. We compared their cell proliferation effects in cultured dog gallbladder epithelial cells (DGBE) to their effects in cultured human pulmonary artery endothelial cells (HPAE). Oxysterols inhibited cell proliferation in a dose-dependent fashion. Oxysterols inhibited cell growth to 50% of control at a higher dose for DGBE cells than for HPAE cells. TriolC was more cytotoxic than 7KC. We also investigated the effect of oxysterols on bile salt-induced mucin secretion by DGBE cells. TriolC suppressed mucin secretion by DGBE cells, whereas 7KC did not. These findings support the hypothesis that biliary oxysterols affect gallbladder mucosal function. Copyright (C) 2000 Federation of European Biochemical Societies. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/febslet | en_HK |
dc.relation.ispartof | FEBS Letters | en_HK |
dc.subject | Cholesterol | en_HK |
dc.subject | Cytotoxicity | en_HK |
dc.subject | Epithelial cell | en_HK |
dc.subject | Gallbladder | en_HK |
dc.subject | Mucin secretion | en_HK |
dc.subject | Oxysterol | en_HK |
dc.title | Cholestan-3β,5α,6β-triol, but not 7-ketocholesterol, suppresses taurocholate-induced mucin secretion by cultured dog gallbladder epithelial cells | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Lee, SP: sumlee@hku.hk | en_HK |
dc.identifier.authority | Lee, SP=rp01351 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/S0014-5793(00)01831-7 | en_HK |
dc.identifier.pmid | 10922480 | en_HK |
dc.identifier.scopus | eid_2-s2.0-0034725459 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0034725459&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 478 | en_HK |
dc.identifier.issue | 1-2 | en_HK |
dc.identifier.spage | 113 | en_HK |
dc.identifier.epage | 118 | en_HK |
dc.identifier.isi | WOS:000088644200023 | - |
dc.publisher.place | Netherlands | en_HK |
dc.identifier.scopusauthorid | Yoshida, T=7501317704 | en_HK |
dc.identifier.scopusauthorid | Klinkspoor, JH=6602590656 | en_HK |
dc.identifier.scopusauthorid | Kuver, R=6701723533 | en_HK |
dc.identifier.scopusauthorid | Wrenn, SP=6603940041 | en_HK |
dc.identifier.scopusauthorid | Kaler, EW=7007157989 | en_HK |
dc.identifier.scopusauthorid | Lee, SP=7601417497 | en_HK |
dc.identifier.issnl | 0014-5793 | - |