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Open Access

Correction

Correction: Alternatively Activated (M2) Macrophage Phenotype Is Inducible by Endothelin-1 in Cultured Human Macrophages

  • Stefano Soldano,
  • Carmen Pizzorni,
  • Sabrina Paolino,
  • Amelia Chiara Trombetta,
  • Paola Montagna,
  • Renata Brizzolara,
  • Barbara Ruaro,
  • Alberto Sulli,
  • Maurizio Cutolo

Fig 1 has an incorrectly duplicated panel. The image for the IL-4 treated CD68 cells is an incorrect duplication of the CD68 ET-1 treated cells. Please see the correct Fig 1 here.

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Fig 1. Evaluation of CD68, CD204 and CD206 expression in cultured THP-1-derived macrophages.

Immunocytochemistry of CD68 (marker of macrophage activation), CD204 and CD206 protein expression in cultured THP-1-derived macrophages (M0 macrophages) treated for 72 hours with ET-1 (100nM) and IL-4 (10ng/mL) alone, or pre-treated with ETA/BRA (bosentan, 10-5M) for 1 hour before being stimulated with ET-1. Cultured M0 macrophages maintained for 72 hours in RPMI at 5% of FBS were used as controls (M0-controls). Immunocytochemistry was performed on four independent in vitro experiments. The detection of protein expression was performed evaluating the same number of cells by light microscopy (magnification 40X).

https://doi.org/10.1371/journal.pone.0175238.g001

Reference

  1. 1. Soldano S, Pizzorni C, Paolino S, Trombetta AC, Montagna P, Brizzolara R, et al. (2016) Alternatively Activated (M2) Macrophage Phenotype Is Inducible by Endothelin-1 in Cultured Human Macrophages. PLoS ONE 11(11): e0166433. pmid:27846260

Citation: Soldano S, Pizzorni C, Paolino S, Trombetta AC, Montagna P, Brizzolara R, et al. (2017) Correction: Alternatively Activated (M2) Macrophage Phenotype Is Inducible by Endothelin-1 in Cultured Human Macrophages. PLoS ONE 12(3): e0175238. https://doi.org/10.1371/journal.pone.0175238

Published: March 30, 2017

Copyright: © 2017 Soldano et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.