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. 2019 May 6;9:6909. doi: 10.1038/s41598-019-43335-y

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© The Author(s) 2019

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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Regulation of Plin2. (A) Immunoblot analysis of Plin2 using protein lysates from control (refed) and O/N fasted C57Bl/6N mice hearts (n = 3). Full-length blots are presented in Supplementary Fig. S7. (B) Quantification of immunoblot analysis on Plin2 (n = 3). (C) Triglyceride content in hearts of control (refed) and overnight fasted mice (n = 3). (D) Confocal microscopy images on C57Bl/6N cardiomyocytes, shown as z-stack 1, 2, 3 and a max stack picture containing 30 z-stacks compromised into one image. Plin2 is shown in green, ORO (LDs) in red and nuclei in blue and co-localization of LDs and Plin2 in yellow (x630 magnification, scale bar: 10 µm). Data are presented as mean ± SEM, *p < 0.05 vs. Plin2^+/+, **p < 0.01 vs. Plin2^+/+. TG, triglycerides; O/N, overnight.