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. 2022 Mar 21;13:114. doi: 10.1186/s13287-022-02795-2

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© The Author(s) 2022

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. 3 — LPLCs exhibit superior proliferation and anti-senescence abilities as compared to SOX9-negative hepatocytes with the progression of cholestasis. Multiple immunofluorescence staining of LPLCs with (A) proliferation marker (Ki67) and (B) anti-senescence marker (p21). Overall percentage (C) and cell cluster percentage (D) of Ki67+ LPLCs and Ki67+ SOX9-negative hepatocytes in different fibrosis stages. Overall percentage (E) and cell cluster percentage (F) of p21+ LPLCs and p21+ SOX9-negative hepatocytes in different fibrosis stages