File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1152/physiolgenomics.00140.2011
- Scopus: eid_2-s2.0-84862099772
- PMID: 22454453
- WOS: WOS:000304367600002
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Differential genomic changes caused by cholesterol-and PUFA-rich diets in regenerated porcine coronary endothelial cells
Title | Differential genomic changes caused by cholesterol-and PUFA-rich diets in regenerated porcine coronary endothelial cells | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Authors | |||||||||||
Keywords | Endothelium Fish oil Microarray Polyunsaturated fatty acids Porcine coronary artery angioplasty Regeneration | ||||||||||
Issue Date | 2012 | ||||||||||
Publisher | American Physiological Society. The Journal's web site is located at http://physiolgenomics.physiology.org/ | ||||||||||
Citation | Physiological Genomics, 2012, v. 44 n. 10, p. 551-561 How to Cite? | ||||||||||
Abstract | Endothelial regeneration and dyslipidemia impair endothelium-dependent relaxation, while supplementation with fish oil (FO) prevents it. The genomic impact of different diets was compared in primary cultures derived from native and regenerated endothelial cells. Pigs were fed with high-cholesterol (CHL) or FO-rich diet. Partial in vivo removal of endothelium was performed to induce endothelial regeneration. Native and regenerated cells were harvested, cultured, and prepared for genomic (microarray experiments, real-time PCR) and proteomic (Western blotting) analysis. The analysis identified genomic changes induced by chronic CHL diet in native cultures resembling those induced by in vivo regeneration, as well as those that could be prevented by FO diet. At the protein level, the reduced and increased presences of endothelial nitric oxide synthase and F2, respectively, observed after regeneration combined with CHL diet were alleviated by FO. The comparison of the differential changes induced by regeneration in vivo in endothelial cells from both diet groups revealed a limited number of genes as the most likely contributors to reduction in endothelium-dependent relaxations in porcine coronary arteries lined with regenerated endothelium. © 2012 the American Physiological Society. | ||||||||||
Persistent Identifier | http://hdl.handle.net/10722/149118 | ||||||||||
ISSN | 2023 Impact Factor: 2.5 2023 SCImago Journal Rankings: 0.999 | ||||||||||
ISI Accession Number ID |
Funding Information: This work was supported by grants from the University of Hong Kong; the Research Grant Council of Hong Kong (HKU 780410M); and the Research Centre of Heart, Brain, Hormone & Healthy Aging of the University of Hong Kong. This study was also supported by an unconditional grant from Les Laboratoires Servier [Neuilly-sur-Seine, France]. | ||||||||||
References | |||||||||||
Grants |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, MYK | en_HK |
dc.contributor.author | Cai, Y | en_HK |
dc.contributor.author | Wang, Y | en_HK |
dc.contributor.author | Liao, SY | en_HK |
dc.contributor.author | Liu, Y | en_HK |
dc.contributor.author | Zhang, Y | en_HK |
dc.contributor.author | Bai, B | en_HK |
dc.contributor.author | Tse, HF | en_HK |
dc.contributor.author | Vanhoutte, PM | en_HK |
dc.date.accessioned | 2012-06-22T06:24:15Z | - |
dc.date.available | 2012-06-22T06:24:15Z | - |
dc.date.issued | 2012 | en_HK |
dc.identifier.citation | Physiological Genomics, 2012, v. 44 n. 10, p. 551-561 | en_HK |
dc.identifier.issn | 1094-8341 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/149118 | - |
dc.description.abstract | Endothelial regeneration and dyslipidemia impair endothelium-dependent relaxation, while supplementation with fish oil (FO) prevents it. The genomic impact of different diets was compared in primary cultures derived from native and regenerated endothelial cells. Pigs were fed with high-cholesterol (CHL) or FO-rich diet. Partial in vivo removal of endothelium was performed to induce endothelial regeneration. Native and regenerated cells were harvested, cultured, and prepared for genomic (microarray experiments, real-time PCR) and proteomic (Western blotting) analysis. The analysis identified genomic changes induced by chronic CHL diet in native cultures resembling those induced by in vivo regeneration, as well as those that could be prevented by FO diet. At the protein level, the reduced and increased presences of endothelial nitric oxide synthase and F2, respectively, observed after regeneration combined with CHL diet were alleviated by FO. The comparison of the differential changes induced by regeneration in vivo in endothelial cells from both diet groups revealed a limited number of genes as the most likely contributors to reduction in endothelium-dependent relaxations in porcine coronary arteries lined with regenerated endothelium. © 2012 the American Physiological Society. | en_HK |
dc.language | eng | en_US |
dc.publisher | American Physiological Society. The Journal's web site is located at http://physiolgenomics.physiology.org/ | - |
dc.relation.ispartof | Physiological Genomics | en_HK |
dc.rights | Physiological Genomics. Copyright © American Physiological Society | - |
dc.subject | Endothelium | en_HK |
dc.subject | Fish oil | en_HK |
dc.subject | Microarray | en_HK |
dc.subject | Polyunsaturated fatty acids | en_HK |
dc.subject | Porcine coronary artery angioplasty | en_HK |
dc.subject | Regeneration | en_HK |
dc.title | Differential genomic changes caused by cholesterol-and PUFA-rich diets in regenerated porcine coronary endothelial cells | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Tse, HF: hftse@hkucc.hku.hk | en_HK |
dc.identifier.email | Vanhoutte, PM: vanhoutt@hku.hk | en_HK |
dc.identifier.authority | Tse, HF=rp00428 | en_HK |
dc.identifier.authority | Vanhoutte, PM=rp00238 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1152/physiolgenomics.00140.2011 | en_HK |
dc.identifier.pmid | 22454453 | - |
dc.identifier.scopus | eid_2-s2.0-84862099772 | en_HK |
dc.identifier.hkuros | 199999 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-84862099772&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 44 | en_HK |
dc.identifier.issue | 10 | en_HK |
dc.identifier.spage | 551 | en_HK |
dc.identifier.epage | 561 | en_HK |
dc.identifier.isi | WOS:000304367600002 | - |
dc.publisher.place | United States | en_HK |
dc.relation.project | Protective effect of lipocalin-2 deficiency on aging- and dietary obesity-induced endothelial dysfunction | - |
dc.identifier.scopusauthorid | Lee, MYK=22980015700 | en_HK |
dc.identifier.scopusauthorid | Cai, Y=55247545000 | en_HK |
dc.identifier.scopusauthorid | Wang, Y=54953511800 | en_HK |
dc.identifier.scopusauthorid | Liao, SY=22433820700 | en_HK |
dc.identifier.scopusauthorid | Liu, Y=54936707200 | en_HK |
dc.identifier.scopusauthorid | Zhang, Y=35785466900 | en_HK |
dc.identifier.scopusauthorid | Bai, B=55247646000 | en_HK |
dc.identifier.scopusauthorid | Tse, HF=7006070805 | en_HK |
dc.identifier.scopusauthorid | Vanhoutte, PM=7202304247 | en_HK |
dc.identifier.issnl | 1094-8341 | - |