Influence of the high density lipoprotein receptor SR-BI on reproductive and cardiovascular pathophysiology
dc.contributor.author | Trigatti, B | |
dc.contributor.author | Rayburn, H | |
dc.contributor.author | Vinals, M | |
dc.contributor.author | Braun, A | |
dc.contributor.author | Miettinen, H | |
dc.contributor.author | Penman, M | |
dc.contributor.author | Hertz, M | |
dc.contributor.author | Schrenzel, M | |
dc.contributor.author | Amigo, L | |
dc.contributor.author | Rigotti, A | |
dc.contributor.author | Krieger, M | |
dc.date.accessioned | 2024-01-10T12:06:04Z | |
dc.date.available | 2024-01-10T12:06:04Z | |
dc.date.issued | 1999 | |
dc.description.abstract | The high density lipoprotein (HDL) receptor SR-BI (scavenger receptor class B type I) mediates the selective uptake of plasma HDL cholesterol by the liver and steroidogenic tissues. As a consequence, SR-BI can influence plasma HDL cholesterol levels, HDL structure, biliary cholesterol concentrations, and the uptake, storage, and utilization of cholesterol by steroid hormone-producing cells. Here we used homozygous null SR-BI knockout mice to show that SR-BI is required for maintaining normal biliary cholesterol levels, oocyte development, and female fertility. We also used SR-BI/apolipoprotein E double homozygous knockout mice to show that SR-BI can protect against early-onset atherosclerosis. Although the mechanisms underlying the effects of SR-BI loss on reproduction and atherosclerosis have not been established, potential causes include changes in (i) plasma lipoprotein levels and/or structure, (ii) cholesterol flux into or out of peripheral tissues (ovary, aortic wall), and (iii) reverse cholesterol transport, as indicated by the significant reduction of gallbladder bile cholesterol levels in SR-BI and SR-BI/apolipoprotein E double knockout mice relative to controls. If SR-BI has similar activities in humans, it may become an attractive target for therapeutic intervention in a variety of diseases. | |
dc.description.funder | NHLBI NIH HHS | |
dc.description.funder | NATIONAL HEART, LUNG, AND BLOOD INSTITUTE | |
dc.fechaingreso.objetodigital | 2024-05-06 | |
dc.format.extent | 6 páginas | |
dc.fuente.origen | WOS | |
dc.identifier.doi | 10.1073/pnas.96.16.9322 | |
dc.identifier.issn | 0027-8424 | |
dc.identifier.pubmedid | MEDLINE:10430941 | |
dc.identifier.uri | https://doi.org/10.1073/pnas.96.16.9322 | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/76111 | |
dc.identifier.wosid | WOS:000081835500099 | |
dc.information.autoruc | Medicina;Rigotti A;S/I;68489 | |
dc.issue.numero | 16 | |
dc.language.iso | en | |
dc.nota.acceso | contenido parcial | |
dc.pagina.final | 9327 | |
dc.pagina.inicio | 9322 | |
dc.publisher | NATL ACAD SCIENCES | |
dc.revista | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | |
dc.rights | acceso restringido | |
dc.subject | APOLIPOPROTEIN-A-I | |
dc.subject | CHOLESTEROL ACYLTRANSFERASE GENE | |
dc.subject | MESSENGER-RNA EXPRESSION | |
dc.subject | SCAVENGER RECEPTOR | |
dc.subject | SELECTIVE UPTAKE | |
dc.subject | ADRENAL-GLAND | |
dc.subject | CELLULAR CHOLESTEROL | |
dc.subject | STEROIDOGENIC CELLS | |
dc.subject | TARGETED MUTATION | |
dc.subject | HDL METABOLISM | |
dc.subject.ods | 03 Good Health and Well-being | |
dc.subject.odspa | 03 Salud y bienestar | |
dc.title | Influence of the high density lipoprotein receptor SR-BI on reproductive and cardiovascular pathophysiology | |
dc.type | artículo | |
dc.volumen | 96 | |
sipa.codpersvinculados | 68489 | |
sipa.index | WOS | |
sipa.index | Scopus | |
sipa.trazabilidad | Carga SIPA;09-01-2024 |
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