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10.1016/j.ebiom.2017.01.006

http://scihub22266oqcxt.onion/10.1016/j.ebiom.2017.01.006
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C5474437!5474437!28111237
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suck abstract from ncbi


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pmid28111237      EBioMedicine 2017 ; 16 (ä): 204-11
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  • Human Neutrophil Peptide 1 Limits Hypercholesterolemia-induced Atherosclerosis by Increasing Hepatic LDL Clearance #MMPMID28111237
  • Paulin N; Döring Y; Kooijman S; Blanchet X; Viola JR; de Jong R; Mandl M; Hendrikse J; Schiener M; von Hundelshausen P; Vogt A; Weber C; Bdeir K; Hofmann SM; Rensen PC; Drechsler M; Soehnlein O
  • EBioMedicine 2017[Feb]; 16 (ä): 204-11 PMID28111237show ga
  • Increases in plasma LDL-cholesterol have unequivocally been established as a causal risk factor for atherosclerosis. Hence, strategies for lowering of LDL-cholesterol may have immediate therapeutic relevance. Here we study the role of human neutrophil peptide 1 (HNP1) in a mouse model of atherosclerosis and identify its potent atheroprotective effect both upon transgenic overexpression and therapeutic delivery. The effect was found to be due to a reduction of plasma LDL-cholesterol. Mechanistically, HNP1 binds to apolipoproteins enriched in LDL. This interaction facilitates clearance of LDL particles in the liver via LDL receptor. Thus, we here identify a non-redundant mechanism by which HNP1 allows for reduction of LDL-cholesterol, a process that may be therapeutically instructed to lower cardiovascular risk.
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