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PLoS One DOI:10.1371/journal.pone.0120295

Modulators of hepatic lipoprotein metabolism identified in a search for small-molecule inducers of tribbles pseudokinase 1 expression.

Publication TypeJournal Article
Year of Publication2015
AuthorsNagiec, MM, Skepner, AP, Negri, J, Eichhorn, M, Kuperwasser, N, Comer, E, Muncipinto, G, Subramanian, A, Clish, C, Musunuru, K, Duvall, JR, Foley, M, Perez, JR, Palmer, MAJ
JournalPLoS One
Volume10
Issue3
Pagese0120295
Date Published2015
ISSN1932-6203
KeywordsCluster Analysis, Gene Expression Profiling, Gene Expression Regulation, Hep G2 Cells, Hepatocytes, High-Throughput Screening Assays, Humans, Intracellular Signaling Peptides and Proteins, Lipid Metabolism, Lipoproteins, Lipoproteins, LDL, Mitogen-Activated Protein Kinases, Oncostatin M, Protein-Serine-Threonine Kinases, Small Molecule Libraries
Abstract

Recent genome wide association studies have linked tribbles pseudokinase 1 (TRIB1) to the risk of coronary artery disease (CAD). Based on the observations that increased expression of TRIB1 reduces secretion of VLDL and is associated with lower plasma levels of LDL cholesterol and triglycerides, higher plasma levels of HDL cholesterol and reduced risk for myocardial infarction, we carried out a high throughput phenotypic screen based on quantitative RT-PCR assay to identify compounds that induce TRIB1 expression in human HepG2 hepatoma cells. In a screen of a collection of diversity-oriented synthesis (DOS)-derived compounds, we identified a series of benzofuran-based compounds that upregulate TRIB1 expression and phenocopy the effects of TRIB1 cDNA overexpression, as they inhibit triglyceride synthesis and apoB secretion in cells. In addition, the compounds downregulate expression of MTTP and APOC3, key components of the lipoprotein assembly pathway. However, CRISPR-Cas9 induced chromosomal disruption of the TRIB1 locus in HepG2 cells, while confirming its regulatory role in lipoprotein metabolism, demonstrated that the effects of benzofurans persist in TRIB1-null cells indicating that TRIB1 is sufficient but not necessary to transmit the effects of the drug. Remarkably, active benzofurans, as well as natural products capable of TRIB1 upregulation, also modulate hepatic cell cholesterol metabolism by elevating the expression of LDLR transcript and LDL receptor protein, while reducing the levels of PCSK9 transcript and secreted PCSK9 protein and stimulating LDL uptake. The effects of benzofurans are not masked by cholesterol depletion and are independent of the SREBP-2 regulatory circuit, indicating that these compounds represent a novel class of chemically tractable small-molecule modulators that shift cellular lipoprotein metabolism in HepG2 cells from lipogenesis to scavenging.

DOI10.1371/journal.pone.0120295
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/25811180?dopt=Abstract

Alternate JournalPLoS ONE
PubMed ID25811180
PubMed Central IDPMC4374785
Grant ListR00 HL098364 / HL / NHLBI NIH HHS / United States
R00-HL098364 / HL / NHLBI NIH HHS / United States