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. 2020 Oct 25;17:320. doi: 10.1186/s12974-020-01970-7

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© The Author(s) 2020

Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 9 — SOX2 siRNA attenuated the loss of cell proliferation and mature neurons and reduced glial differentiation in the hippocampus from sepsis-associated encephalopathy mice. Representative immunofluorescence micrographs showing (a) BrdU⁺/DCX⁺ cells, (b) BrdU⁺/GFAP⁺ glial cells and (c) BrdU⁺/NeuN⁺ neurons in hippocampal dentate gyrus of CLP mice injected with SOX2 siRNA. Magnification: × 200. Bar = 100 μm. Quantification of immunofluorescent cells staining positive for (d) BrdU/DCX, (e) BrdU/GFAP or (f) Brdu/NeuN. *p < 0.05; **p < 0.01. Abbreviations: CLP, cecal ligation and perforation; si-SOX2, SOX2 siRNA