The impact of severe LDL receptor mutations on SREBP-pathway regulation in homozygous familial hypercholesterolemia (FH)

• Published in: Gene 2012-05, Vol.499 (1), p.218-222
• Main Authors: Soufi, Muhidien, Ruppert, Volker, Kurt, Bilgen, Schaefer, Juergen R.
• Format: Article
• Language: English
• Subjects: ABCA1; Adult; ATP Binding Cassette Transporter 1; ATP-Binding Cassette Transporters - genetics; ATP-Binding Cassette Transporters - metabolism; ATP-Binding Cassette Transporters - physiology; Cells, Cultured; cholesterol; Familial hypercholesterolemia; Female; fibroblasts; Fibroblasts - metabolism; Fibroblasts - pathology; gene expression; genes; genetic disorders; HEK293 Cells; heterozygosity; homeostasis; homozygosity; Homozygote; Humans; hypercholesterolemia; Hyperlipoproteinemia Type II - genetics; Hyperlipoproteinemia Type II - metabolism; Hyperlipoproteinemia Type II - pathology; LDL receptor; low density lipoprotein; Male; Models, Biological; mutation; Mutation - physiology; patients; Primary Cell Culture; receptors; Receptors, LDL - genetics; Scavenger Receptors, Class B - genetics; Scavenger Receptors, Class B - metabolism; Scavenger Receptors, Class B - physiology; Severity of Illness Index; Signal Transduction - genetics; Signal Transduction - physiology; SR-BI; SREBP pathway; Sterol Regulatory Element Binding Proteins - genetics; Sterol Regulatory Element Binding Proteins - metabolism; Twins, Monozygotic
• ISSN: 0378-1119; 1879-0038
• DOI: 10.1016/j.gene.2012.02.031

Familial hypercholesterolemia (FH), Niemann–Pick disease type C (NPC) and Tangier disease (TD) are genetic inherited disorders with impaired processing of cholesterol, caused by mutations in genes that regulate cellular uptake, intracellular movement and transport of cholesterol. Various studies have shown a crucial regulatory role of the SREBP-pathway for cellular cholesterol homeostasis in these diseases. Since cholesterol is an essential structural component of cells, we assessed the impact of a severe FH causing LDLR mutation (FH p.W556R) on the SREBP pathway in primary FH fibroblasts. Primary FH fibroblasts derived from patients with the LDL receptor mutation p.W556R were used for gene expression experiments. Gene expression studies revealed increased expressions of SREBP regulated genes HMGCR, LDLR, SREBP-2, SREBP-1, SR-BI, INSIG-1, but interestingly not SCAP. In contrast expression of ABCA1, was strongly decreased in homozygous, but not in heterozygous p.W556R fibroblasts. Gene expression experiments with LDL receptor lacking primary FH fibroblasts, revealed that SR-BI and ABCA1 are important regulators for cholesterol acquisition in FH cells, consistent with findings in cells from NPC and TD patients. ► We examined SREPB pathway regulation in FH-Fibroblasts. ► SREBP-2 activates SR-BI expression in FH-Fibroblasts. ► SREBP-2 mediated ABCA1 expression is decreased in homozygous FH-Fibroblasts. ► Cholesterol pools regulate SREBP-2 function for ABCA1 transcription in FH.