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. 2021 Jul 8;31(9):965–979. doi: 10.1038/s41422-021-00532-7

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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 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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Fig. 3 — a Representative images and quantifications of the BODIPY493/503 staining of the endogenous LDs in the 3T3-L1 differentiated adipocytes treated with the indicated compounds (LD·ATTECs: C1, C2, C3 and C4). Bars indicate means ± SEM. The LD number per cell and averaged LD size in each field were quantified by ImageJ (particle analysis) in a blinded manner. ns, P > 0.05; *P < 0.05; **P < 0.01; ***P < 0.001; ^$P < 0.0001 by one-way ANOVA (P values have been indicated) and Dunnett’s post hoc tests (compared to the DMSO group, if the ANOVA test showed significance). b Similar to a, but in cells transfected with the indicated siRNAs 48 h before treatment with compounds.