Quantitative HDL Proteomics Identifies Peroxiredoxin-6 as a Biomarker of Human Abdominal Aortic Aneurysm.
Quantitative HDL Proteomics Identifies Peroxiredoxin-6 as a Biomarker of Human Abdominal Aortic Aneurysm.
复制标题
DOI:
10.1038/srep38477
复制
发表时间:
2016-12-09
影响因子:
4.6
通讯作者:
Martin-Ventura JL
中科院分区:
文献类型:
--
作者:
Burillo E;Jorge I;Martínez-López D;Camafeita E;Blanco-Colio LM;Trevisan-Herraz M;Ezkurdia I;Egido J;Michel JB;Meilhac O;Vázquez J;Martin-Ventura JL
High-density lipoproteins (HDLs) are complex protein and lipid assemblies whose composition is known to change in diverse pathological situations. Analysis of the HDL proteome can thus provide insight into the main mechanisms underlying abdominal aortic aneurysm (AAA) and potentially detect novel systemic biomarkers. We performed a multiplexed quantitative proteomics analysis of HDLs isolated from plasma of AAA patients (N = 14) and control study participants (N = 7). Validation was performed by western-blot (HDL), immunohistochemistry (tissue), and ELISA (plasma). HDL from AAA patients showed elevated expression of peroxiredoxin-6 (PRDX6), HLA class I histocompatibility antigen (HLA-I), retinol-binding protein 4, and paraoxonase/arylesterase 1 (PON1), whereas α-2 macroglobulin and C4b-binding protein were decreased. The main pathways associated with HDL alterations in AAA were oxidative stress and immune-inflammatory responses. In AAA tissue, PRDX6 colocalized with neutrophils, vascular smooth muscle cells, and lipid oxidation. Moreover, plasma PRDX6 was higher in AAA (N = 47) than in controls (N = 27), reflecting increased systemic oxidative stress. Finally, a positive correlation was recorded between PRDX6 and AAA diameter. The analysis of the HDL proteome demonstrates that redox imbalance is a major mechanism in AAA, identifying the antioxidant PRDX6 as a novel systemic biomarker of AAA.
登录
查看更多内容
DOI:
10.1161/atvbaha.110.214429
发表时间:
2011-04-01
影响因子:
8.7
作者:
Martinez-Pinna, Roxana;Ramos-Mozo, Priscila;Martin-Ventura, Jose L.
通讯作者:
Martin-Ventura, Jose L.
影响因子:
4.8
作者:
Chatterjee, Shampa;Feinstein, Sheldon I.;Fisher, Aron B.
通讯作者:
Fisher, Aron B.
影响因子:
2
作者:
Martinez-Pinna, Roxana;de Peredo, Anne Gonzalez;Luis Martin-Ventura, Jose
通讯作者:
Luis Martin-Ventura, Jose
影响因子:
7.4
作者:
Kwon J;Wang A;Burke DJ;Boudreau HE;Lekstrom KJ;Korzeniowska A;Sugamata R;Kim YS;Yi L;Ersoy I;Jaeger S;Palaniappan K;Ambruso DR;Jackson SH;Leto TL
通讯作者:
Leto TL
DOI:
10.1016/j.bbamcr.2011.11.014
发表时间:
2012-02-01
影响因子:
5.1
作者:
Ambruso, Daniel R.;Ellison, Michael A.;Leto, Thomas L.
通讯作者:
Leto, Thomas L.