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. 2023 Nov 28;24:300. doi: 10.1186/s12931-023-02606-z

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© The Author(s) 2023

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 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. 8 — TGF-β1 induces the differentiation of LR-MSCs into myofibroblasts by modulating the METTL3/miR-21/PTEN pathway. A, B The mRNA and protein expression levels of PTEN in LR-MSCs with or without METTL3 silencing, combined with or without treatment with TGF-β1 and miR-21 mimics. C–E The mRNA and protein expression levels of myofibroblast markers (α-SMA, type I collagen, and vimentin) in LR-MSCs with or without METTL3 silencing, PTEN overexpression, and treatment with TGF-β1 and miR-21 mimics. β-Actin was used as a reference gene. Scale bars = 20 μm, **P < 0.01