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. 2019 May 6;9:6905. doi: 10.1038/s41598-019-43413-1

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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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The localization of large ribosomal proteins were nuclear accumulation in treatment groups. (A) The HEK293T cells expressing RpL23a-GFP were treated with different concentrations of thallium. And the protein localization of RpL23a was imaged by fluorescent microscopy. Cell nuclei were stained with Hoechst. The cytoplasmic intensity of RpL23a was measured with Image J and shown in the bar graph (n = 20). Scale bars, 25 μm. Error bars represent SD. Student’s t tests relative to the control were performed. *p < 0.05, **p < 0.01. (B,C) Immunofluorescence staining of RpL36 (B) and RpS3a (C) with anti-RpL36 and anti-RpS3a. DNA was stained by DAPI. Scale bars, 20 μm.