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. 2021 Sep 30;12:743202. doi: 10.3389/fendo.2021.743202

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Copyright © 2021 Xie, Chen, Xu, Li, Ni, Hou, Chen, Chang, Yang, Wang, He, Chen, Qian, Luo, Zhang, Li, Zhu, Ji and Liu

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Increased nuclear transporting of Hsp90α in MAFLD mice. (A) Immunohistochemical staining of the liver section with Hsp90α. (B) Semiquantitative analysis of the expression of Hsp90α in the nucleus and cytoplasm in the immunohistochemical staining. (C) Immunofluorescence staining to investigate the locating of Hsp90α. DAPI (blue) marked the nucleus, F4/80 (red) marked Kupffer cells, albumin (green) marked hepatocytes. (D) Colocation analysis of Hsp90α and albumin, DAPI, F4/80 in immunofluorescence staining. Data are presented as mean ± SEM. The significance among groups was determined using the two-way ANOVA with LSD’s multiple comparisons test (n = 4 in CON-NS group, n = 6 in CON-GGA group, n = 7 in NASH-NS group, n = 7 in NASH-GGA group). *p < 0.05, **p < 0.01, ***p < 0.001.