Ontology highlight
ABSTRACT: Background
High circulating levels of Lp(a) (lipoprotein[a]) increase the risk of atherosclerosis and calcific aortic valve disease, affecting millions of patients worldwide. Although atherosclerosis is commonly treated with low-density lipoprotein-targeting therapies, these do not reduce Lp(a) or risk of calcific aortic valve disease, which has no available drug therapies. Targeting Lp(a) production and catabolism may provide therapeutic benefit, but little is known about Lp(a) cellular uptake.Methods
Here, unbiased ligand-receptor capture mass spectrometry was used to identify MFSD5 (major facilitator superfamily domain containing 5) as a novel receptor/cofactor involved in Lp(a) uptake.Results
Reducing MFSD5 expression by a computationally identified small
SUBMITTER: Rogers MA
PROVIDER: S-EPMC10842618 | biostudies-literature | 2024 Jan
REPOSITORIES: biostudies-literature