Dietary Pyrophosphate Modulates Calcification in a Mouse Model of Pseudoxanthoma Elasticum: Implication for Treatment of Patients

التفاصيل البيبلوغرافية
العنوان: Dietary Pyrophosphate Modulates Calcification in a Mouse Model of Pseudoxanthoma Elasticum: Implication for Treatment of Patients
المؤلفون: Pomozi, Viola, Julian, Charnelle B., Zoll, Janna, Pham, Kevin, Kuo, Sheree, Tőkési, Natália, Martin, Ludovic, Váradi, András, Le Saux, Olivier
المصدر: Journal of Investigative Dermatology; May 2019, Vol. 139 Issue: 5 p1082-1088, 7p
مستخلص: Pseudoxanthoma elasticum is a heritable disease caused by ABCC6deficiency. Patients develop ectopic calcification in skin, eyes, and vascular tissues. ABCC6, primarily found in liver and kidneys, mediates the cellular efflux of ATP, which is rapidly converted into inorganic pyrophosphate (PPi), a potent inhibitor of calcification. Pseudoxanthoma elasticum patients and Abcc6–/–mice display reduced PPi levels in plasma and peripheral tissues. Pseudoxanthoma elasticum is currently incurable, although some palliative treatments exist. In recent years, we have successfully developed therapeutic methodologies to compensate the PPi deficit in animal models and humans. Here, we inadvertently discovered that modulating dietary PPi can also be an effective approach to reducing calcification in Abcc6–/–mice. Our findings were prompted by a change in institutional rodent diet. The new chow was enriched in PPi, which increased plasma PPi, and significantly reduced mineralization in Abcc6–/–mice. We also found that dietary PPi is readily absorbed in humans. Our results suggest that the consumption of food naturally or artificially enriched in PPi represents a possible intervention to mitigate calcification progression in pseudoxanthoma elasticum, that dietary preferences of patients may explain pseudoxanthoma elasticum heterogeneous manifestations, and that animal chow has the potential to influence data reproducibility.
قاعدة البيانات: Supplemental Index
الوصف
تدمد:0022202X
15231747
DOI:10.1016/j.jid.2018.10.040