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. 2018 Jan 17;8:902. doi: 10.1038/s41598-017-18832-7

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Efficiency of monocyte-to-macrophage differentiation is regulated by PPM1A. THP-1, THP-PPM1A, and THP-ΔPPM1A monocytes were treated with (A) PMA (100 ng/ml) or (B) Bryostatin (10 nM) to induce macrophage differentiation. Differentiation (adherence) was measured kinetically by the Real-time Cell Analysis (RTCA) system. The Cell Index (CI) is an arbitrary unit proportional to the strength of adherence. CI measurements were made every 30 min and represent the average of 3 independent wells.