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. 2023 Mar 29;20:86. doi: 10.1186/s12974-023-02762-5

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© The Author(s) 2023

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. 7 — Effect of HCA2 on the expression of iNOS and Arg-1 in microglia. We, respectively, treated BV2 cells with SiHCA2 (25 nM, 24 h), MK2206 (10 μM, 4 h) and SiPPARγ (25 nM, 24 h), and then treated with NA (1 mM) and LPS (100 ng/mL) for 24 h. After that, we examined the expression of iNOS and Arg-1 in microglia. A The expression of iNOS was detected using the immunofluorescence staining (the bar represents 20 μm). B The expression of Arg-1 was detected using the immunofluorescence staining (the bar represents 20 μm)