دورية أكاديمية
Defective extracellular pyrophosphate metabolism promotes vascular calcification in a mouse model of Hutchinson-Gilford progeria syndrome that is ameliorated on pyrophosphate treatment
| العنوان: | Defective extracellular pyrophosphate metabolism promotes vascular calcification in a mouse model of Hutchinson-Gilford progeria syndrome that is ameliorated on pyrophosphate treatment |
|---|---|
| المؤلفون: | Villa-Bellosta, Ricardo, Rivera-Torres, Jose, Osorio, Fernando G, Acin-Perez, Rebeca, Enriquez, Jose Antonio, López-Otín, Carlos, Andres, Vicente |
| المساهمون: | Ministerio de Economía y Competitividad (España), Instituto de Salud Carlos III, Progeria Research Foundation, Botín Foundation, Fundación Cajastur, Fundación ProCNIC |
| سنة النشر: | 2013 |
| المجموعة: | REPISALUD (REPositorio Institucional en SALUD del Instituto de Salud Carlos III - ISCIII) |
| مصطلحات موضوعية: | ATP, Hutchinson-Gilford progeria syndrome, muscle, Progerin, Pyrophosphate, Tissue-non specific alkaline phosphatase, Vascular calcification, Smooth, Adenosine Triphosphate, Alkaline Phosphatase, Animals, Aorta, Cells, Cultured, Diphosphates, Disease Models, Animal, Lamin Type A, Male, Mice, Inbred C57BL, Mutant Strains, Mitochondria, Vascular, Progeria, Treatment Outcome |
| الوصف: | BACKGROUND: Progerin is a mutant form of lamin A responsible for Hutchinson-Gilford progeria syndrome (HGPS), a premature aging disorder characterized by excessive atherosclerosis and vascular calcification that leads to premature death, predominantly of myocardial infarction or stroke. The goal of this study was to investigate mechanisms that cause excessive vascular calcification in HGPS. METHODS AND RESULTS: We performed expression and functional studies in wild-type mice and knock-in Lmna(G609G/+) mice expressing progerin, which mimic the main clinical manifestations of HGPS. Lmna(G609G/+) mice showed excessive aortic calcification, and primary aortic vascular smooth muscle cells from these progeroid animals had an impaired capacity to inhibit vascular calcification. This defect in progerin-expressing vascular smooth muscle cells is associated with increased expression and activity of tissue-nonspecific alkaline phosphatase and mitochondrial dysfunction, which leads to reduced ATP synthesis. Accordingly, Lmna(G609G/+) vascular smooth muscle cells are defective for the production and extracellular accumulation of pyrophosphate, a major inhibitor of vascular calcification. We also found increased alkaline phosphatase activity and reduced ATP and pyrophosphate levels in plasma of Lmna(G609G/+) mice without changes in phosphorus and calcium. Treatment with pyrophosphate inhibited vascular calcification in progeroid mice. CONCLUSIONS: Excessive vascular calcification in Lmna(G609G) mice is caused by reduced extracellular accumulation of pyrophosphate that results from increased tissue-nonspecific alkaline phosphatase activity and diminished ATP availability caused by mitochondrial dysfunction in vascular smooth muscle cells. Excessive calcification is ameliorated on pyrophosphate treatment. These findings reveal a previously undefined pathogenic process in HGPS that may also contribute to vascular calcification in normal aging, because progerin progressively accumulates in the vascular tissue of individuals ... |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| تدمد: | 0009-7322 1524-4539 |
| العلاقة: | Postprint; https://doi.org/10.1161/CIRCULATIONAHA.112.000571Test; info:eu-repo/grantAgreement/ES/SAF2010-16044; info:eu-repo/grantAgreement/ES/RD06/0014/0021; info:eu-repo/grantAgreement/ES/RD12/0042/0028; info:eu-repo/grantAgreement/ES/JCI-2011-09663; Circulation. 2013; 127(24):2442-51; http://hdl.handle.net/20.500.12105/7754Test; Circulation |
| DOI: | 10.1161/CIRCULATIONAHA.112.000571 |
| الإتاحة: | https://doi.org/20.500.12105/7754Test https://doi.org/10.1161/CIRCULATIONAHA.112.000571Test https://hdl.handle.net/20.500.12105/7754Test |
| حقوق: | http://creativecommons.org/licenses/by-nc-nd/4.0Test/ ; Attribution-NonCommercial-NoDerivatives 4.0 Internacional ; info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.72CCF3D4 |
| قاعدة البيانات: | BASE |
Full Text Finder | تدمد: | 00097322 15244539 |
|---|---|
| DOI: | 10.1161/CIRCULATIONAHA.112.000571 |