Details

Autor(en) / Beteiligte

• Abifadel, Marianne
• Guerin, Maryse
• Benjannet, Suzanne
• Rabès, Jean-Pierre
• Le Goff, Wilfried
• Julia, Zélie
• Hamelin, Josée
• Carreau, Valérie
• Varret, Mathilde
• Bruckert, Eric
• Tosolini, Laurent
• Meilhac, Olivier
• Couvert, Philippe
• Bonnefont-Rousselot, Dominique
• Chapman, John
• Carrié, Alain
• Michel, Jean-Baptiste
• Prat, Annik
• Seidah, Nabil G
• Boileau, Catherine

Titel

Identification and characterization of new gain-of-function mutations in the PCSK9 gene responsible for autosomal dominant hypercholesterolemia

Ist Teil von

• Atherosclerosis, 2012-08, Vol.223 (2), p.394-400

Ort / Verlag

Amsterdam: Elsevier Ireland Ltd

Erscheinungsjahr

2012

Quelle

MEDLINE

Beschreibungen/Notizen

• Abstract Background The identification of mutations in PCSK9 (proprotein convertase subtilisin kexin9) in autosomal dominant hypercholesterolemia (ADH), has revealed the existence of a new player in cholesterol homeostasis. PCSK9 has been shown to enhance the degradation of the LDL receptor (LDLR) at the cell surface. Gain-of-function mutations of PCSK9 induce ADH and are very rare, but their identification is crucial in studying PCSK9's role in hypercholesterolemia, its detailed trafficking pathway and its impact on the LDLR. Methods In order to identify new mutations and understand the exact mechanisms of action of mutated PCSK9, PCSK9 was sequenced in 75 ADH patients with no mutations in the LDLR or APOB genes. Functional analyses in cell culture were conducted and the impact of novel PCSK9 mutations on the quantitative and qualitative features of lipoprotein particles and on the HDL-mediated cellular cholesterol efflux was studied. Results Among these 75 ADH probands with no mutations in the LDLR or APOB genes, four gain-of-function mutations of PCSK9 were identified, of which two were novel: the p.Leu108Arg and the p.Asp35Tyr substitutions. In vitro studies of their consequences on the activity of PCSK9 on cell surface levels of LDLR showed that the p.Leu108Arg mutation clearly results in a gain-of-function, while the p.Asp35Tyr mutation created a novel Tyr-sulfation site, which may enhance the intracellular activity of PCSK9. Conclusion These data further contribute to the characterization of PCSK9 mutations and to better understanding of the impact on cholesterol metabolism of this new therapeutic target.