An enzyme-linked immunosorbent assay for measuring GPIHBP1 levels in human plasma or serum.
An enzyme-linked immunosorbent assay for measuring GPIHBP1 levels in human plasma or serum.
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DOI:
10.1016/j.jacl.2017.10.022
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发表时间:
2018-01
影响因子:
4.4
通讯作者:
Nakajima K
中科院分区:
文献类型:
--
作者:
Miyashita K;Fukamachi I;Nagao M;Ishida T;Kobayashi J;Machida T;Nakajima K;Murakami M;Ploug M;Beigneux AP;Young SG;Nakajima K
GPIHBP1, a glycosylphosphatidylinositol (GPI)-anchored protein of capillary endothelial cells, transports lipoprotein lipase to the capillary lumen and is essential for the lipolytic processing of triglyceride-rich lipoproteins. Because some GPI-anchored proteins have been detected in plasma, we tested whether GPIHBP1 is present in human blood, and whether GPIHBP1 deficiency or a history of cardiovascular disease affected GPIHBP1 circulating levels. We developed two monoclonal antibodies against GPIHBP1and used the antibodies to established a sandwich ELISA to measure GPIHBP1 levels in human blood. The GPIHBP1 ELISA was linear in the 8–500 pg/ml range and allowed the quantification of GPIHBP1 in serum and in pre- and post-heparin plasma (including lipemic samples). GPIHBP1 was undetectable in the plasma of subjects with null mutations in GPIHBP1. Serum GPIHBP1 median levels were 849 pg/ml (range: 740–1014) in healthy volunteers (n = 28) and 1087 pg/ml (range: 877–1371) in patients with a history of cardiovascular or metabolic disease (n = 415). There was an extremely small inverse correlation between GPIHBP1 and triglyceride levels (r = 0.109; P <0.0275). GPIHBP1 levels tended to be slightly higher in patients who had a major cardiovascular event after revascularization. We developed an ELISA for quantifying GPIHBP1 in human blood. This assay will be useful to identify patients with GPIHBP1 deficiency and patients with GPIHBP1 autoantibodies. The potential of plasma GPIHBP1 as a biomarker for metabolic or cardiovascular disease is yet questionable but needs additional testing.
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影响因子:
20.1
作者:
Beigneux AP;Fong LG;Bensadoun A;Davies BS;Oberer M;Gårdsvoll H;Ploug M;Young SG
通讯作者:
Young SG
影响因子:
4.8
作者:
Plengpanich, Wanee;Young, Stephen G.;Beigneux, Anne P.
通讯作者:
Beigneux, Anne P.
影响因子:
6.5
作者:
Olivecrona, Gunilla;Ehrenborg, Ewa;Hernell, Olle
通讯作者:
Hernell, Olle
影响因子:
1.6
作者:
Gardsvoll, Henrik;Hansen, Line V.;Ploug, Michael
通讯作者:
Ploug, Michael
DOI:
10.1161/atvbaha.109.186577
发表时间:
2009-06
期刊:
Arteriosclerosis, thrombosis, and vascular biology
影响因子:
--
作者:
Beigneux AP;Franssen R;Bensadoun A;Gin P;Melford K;Peter J;Walzem RL;Weinstein MM;Davies BS;Kuivenhoven JA;Kastelein JJ;Fong LG;Dallinga-Thie GM;Young SG
通讯作者:
Young SG