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. 2021 Apr 12;11:7928. doi: 10.1038/s41598-021-85119-3

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© The Author(s) 2021

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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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IL8 and MCP1 ELISA with supernatants from SGBS-derived cells. SGBS-derived cells were exposed to DEHP [50 µg/ml] from d0–d4 of adipogenesis. Samples of the cell supernatant were taken at d4 and d8 of differentiation. IL8 and MCP1 ELISA was performed. The data were statistically analyzed by one-way ANOVA on ranks with the Student–Newman–Keuls method. N = 7, n = 1 (4 pooled wells); *p ≤ 0.05 DEHP vs. DMSO at d4 or d8; ^ap ≤ 0.05 DMSO d4 vs. DMSO d8, DEHP d4 vs. DEHP d8.