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新型磷酸盐激活的巨噬细胞通过增加细胞外ATP和焦磷酸盐来预防异位钙化。

Novel phosphate-activated macrophages prevent ectopic calcification by increasing extracellular ATP and pyrophosphate.

作者信息

Villa-Bellosta Ricardo, Hamczyk Magda R, Andrés Vicente

机构信息

Centro Nacional de Investigaciones CardiovascularesCarlos III (CNIC), Madrid, Spain.

Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), Madrid, Spain.

出版信息

PLoS One. 2017 Mar 31;12(3):e0174998. doi: 10.1371/journal.pone.0174998. eCollection 2017.

Abstract

PURPOSE

Phosphorus is an essential nutrient involved in many pathobiological processes. Less than 1% of phosphorus is found in extracellular fluids as inorganic phosphate ion (Pi) in solution. High serum Pi level promotes ectopic calcification in many tissues, including blood vessels. Here, we studied the effect of elevated Pi concentration on macrophage polarization and calcification. Macrophages, present in virtually all tissues, play key roles in health and disease and display remarkable plasticity, being able to change their physiology in response to environmental cues.

METHODS AND RESULTS

High-throughput transcriptomic analysis and functional studies demonstrated that Pi induces unpolarized macrophages to adopt a phenotype closely resembling that of alternatively-activated M2 macrophages, as revealed by arginine hydrolysis and energetic and antioxidant profiles. Pi-induced macrophages showed an anti-calcifying action mediated by increased availability of extracellular ATP and pyrophosphate.

CONCLUSION

We conclude that the ability of Pi-activated macrophages to prevent calcium-phosphate deposition is a compensatory mechanism protecting tissues from hyperphosphatemia-induced pathologic calcification.

摘要

目的

磷是一种参与多种病理生物学过程的必需营养素。在细胞外液中,以无机磷酸根离子(Pi)形式存在于溶液中的磷不到1%。高血清Pi水平会促进包括血管在内的许多组织发生异位钙化。在此,我们研究了升高的Pi浓度对巨噬细胞极化和钙化的影响。巨噬细胞几乎存在于所有组织中,在健康和疾病中发挥关键作用,并且具有显著的可塑性,能够根据环境线索改变其生理状态。

方法与结果

高通量转录组分析和功能研究表明,Pi诱导未极化的巨噬细胞呈现出一种与替代性激活的M2巨噬细胞非常相似的表型,这通过精氨酸水解以及能量和抗氧化特征得以揭示。Pi诱导的巨噬细胞表现出由细胞外ATP和焦磷酸可用性增加介导的抗钙化作用。

结论

我们得出结论,Pi激活的巨噬细胞预防磷酸钙沉积的能力是一种保护组织免受高磷血症诱导的病理性钙化的代偿机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc6/5376322/51e0405299cc/pone.0174998.g001.jpg

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