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

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.

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Animals
  • Antioxidants / metabolism
  • Calcium / metabolism
  • Diphosphates / metabolism*
  • Flow Cytometry
  • Macrophages / drug effects*
  • Macrophages / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Phosphates / pharmacology*
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Vascular Calcification / metabolism*

Substances

  • Antioxidants
  • Diphosphates
  • Phosphates
  • diphosphoric acid
  • Adenosine Triphosphate
  • Calcium

Grants and funding

The Spanish Ministerio de Economía y Competitividad (MINECO) supports R.V.-B. (“Juan de la Cierva” JCI-2011-09663 and SAF-2014-60699-JIN postdoctoral contracts) and M.R.H. (FPI predoctoral contract BES-2011-043938). This study was supported by research grants to V.A. from MINECO (SAF2013-4663-R) and the Instituto de Salud Carlos III (RD12/0042/0028) with co-funding from the Fondo Europeo de Desarrollo Regional (FEDER). The CNIC is supported by the MINECO and the Pro-CNIC Foundation, and is a Severo Ochoa Center of Excellence (MINECO award SEV-2015-0505). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.