Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Choi, Seungbum | - |
dc.contributor.author | Park, Yae Eun | - |
dc.contributor.author | Cheon, Eun Jeong | - |
dc.contributor.author | Kim, Kyeong Yeon | - |
dc.contributor.author | Kim, Miso | - |
dc.contributor.author | Ann, Soo-jin | - |
dc.contributor.author | Noh, Hye-Min | - |
dc.contributor.author | Lee, Jaeho | - |
dc.contributor.author | Lee, Chan Joo | - |
dc.contributor.author | Lee, Seung-Taek | - |
dc.contributor.author | Lee, Cheolju | - |
dc.contributor.author | Lee, Ji Eun | - |
dc.contributor.author | Lee, Sang-Hak | - |
dc.date.accessioned | 2024-01-19T18:02:58Z | - |
dc.date.available | 2024-01-19T18:02:58Z | - |
dc.date.created | 2021-09-04 | - |
dc.date.issued | 2020-03 | - |
dc.identifier.issn | 1738-5520 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/118928 | - |
dc.description.abstract | Background and Objectives: Recent studies have examined the structure-function relationship of high-density lipoprotein (HDL). This study aimed to identify and rank HDL-associated proteins involved in several biological function of HDL. Methods: HDLs isolated from 48 participants were analyzed. Cholesterol efflux capacity, effect of HDL on nitric oxide production, and vascular cell adhesion molecule-1 expression were assessed. The relative abundance of identified proteins in the highest vs. lowest quartile was expressed using the normalized spectral abundance factor ratio. Results: After adjustment by multiple testing, six proteins, thyroxine-binding globulin, alpha-1B-glycoprotein, plasma serine protease inhibitor, vitronectin, angiotensinogen, and serum amyloid A-4, were more abundant (relative abundance ratio >= 2) in HDLs with the highest cholesterol efflux capacity. In contrast, three proteins, complement C4-A, alpha-2-macroglobulin, and immunoglobulin mu chain C region, were less abundant (relative abundance ratio <0.5). In terms of nitric oxide production and vascular cell adhesion molecule-1 expression, no proteins showed abundance ratios >= 2 or <0.5 after adjustment. Proteins correlated with the functional parameters of HDL belonged to diverse biological categories. Conclusions: In summary, this study ranked proteins showing higher or lower abundance in HDLs with high functional capacities and newly identified multiple proteins linked to cholesterol efflux capacity. | - |
dc.language | English | - |
dc.publisher | KOREAN SOC CARDIOLOGY | - |
dc.subject | EPITHELIUM-DERIVED FACTOR | - |
dc.subject | GROWTH-FACTOR-I | - |
dc.subject | BINDING PROTEIN-3 | - |
dc.subject | ANTIINFLAMMATORY PROPERTIES | - |
dc.subject | HDL | - |
dc.subject | ATHEROSCLEROSIS | - |
dc.subject | VITRONECTIN | - |
dc.subject | SUPPRESSION | - |
dc.subject | ACTIVATION | - |
dc.subject | PATHWAYS | - |
dc.title | Novel Associations between Related Proteins and Cellular Effects of High-Density Lipoprotein | - |
dc.type | Article | - |
dc.identifier.doi | 10.4070/kcj.2019.0195 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | KOREAN CIRCULATION JOURNAL, v.50, no.3, pp.236 - 247 | - |
dc.citation.title | KOREAN CIRCULATION JOURNAL | - |
dc.citation.volume | 50 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | 236 | - |
dc.citation.endPage | 247 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
dc.identifier.kciid | ART002558874 | - |
dc.identifier.wosid | 000517831100005 | - |
dc.identifier.scopusid | 2-s2.0-85081545168 | - |
dc.relation.journalWebOfScienceCategory | Cardiac & Cardiovascular Systems | - |
dc.relation.journalResearchArea | Cardiovascular System & Cardiology | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | EPITHELIUM-DERIVED FACTOR | - |
dc.subject.keywordPlus | GROWTH-FACTOR-I | - |
dc.subject.keywordPlus | BINDING PROTEIN-3 | - |
dc.subject.keywordPlus | ANTIINFLAMMATORY PROPERTIES | - |
dc.subject.keywordPlus | HDL | - |
dc.subject.keywordPlus | ATHEROSCLEROSIS | - |
dc.subject.keywordPlus | VITRONECTIN | - |
dc.subject.keywordPlus | SUPPRESSION | - |
dc.subject.keywordPlus | ACTIVATION | - |
dc.subject.keywordPlus | PATHWAYS | - |
dc.subject.keywordAuthor | Atherosclerosis | - |
dc.subject.keywordAuthor | Cardiovascular diseases | - |
dc.subject.keywordAuthor | Proteomics | - |
dc.subject.keywordAuthor | Lipoproteins | - |
dc.subject.keywordAuthor | Immunity | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.