Sortilin: An unusual suspect in cholesterol metabolism From GWAS identification to in vivo biochemical analyses, sortilin has been identified as a novel mediator of human lipoprotein metabolism

被引:31
作者
Dube, Joseph B.
Johansen, Christopher T.
Hegele, Robert A. [1 ]
机构
[1] Robarts Res Inst, Dept Biochem, London, ON N6A 5C1, Canada
关键词
cardiovascular disease; functional genomics; genome-wide association studies; lipoprotein metabolism; low-density lipoprotein cholesterol; MESENCHYMAL STEM-CELLS; VPS10P DOMAIN; CARDIOVASCULAR-DISEASE; LDL-CHOLESTEROL; GENE-EXPRESSION; ASSOCIATION; RECEPTOR; PROTEIN; LOCI; ENDOCYTOSIS;
D O I
10.1002/bies.201100003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The concentration of low-density lipoprotein (LDL) cholesterol (C) in plasma is a key determinant of cardiovascular disease risk and human genetic studies have long endeavoured to elucidate the pathways that regulate LDL metabolism. Massive genome-wide association studies (GWASs) of common genetic variation associated with LDL-C in the population have implicated SORT1 in LDL metabolism. Using experimental paradigms and standards appropriate for understanding the mechanisms by which common variants alter phenotypic expression, three recent publications have presented divergent and even contradictory findings. Interestingly, although these reports each linked SORT1 to LDL metabolism, they did not agree on a mechanism to explain the association. Here, we review recent mechanistic studies of SORT1 the first gene identified by GWAS as a determinant of plasma LDL-C to be evaluated mechanistically.
引用
收藏
页码:430 / 437
页数:8
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