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. 2024 Oct 1;24:1166. doi: 10.1186/s12903-024-04882-7

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© The Author(s) 2024

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/.

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Fig. 5 — The effects of decellularized extracellular matrix derived from dental pulp stem cells (DPSCs) on gingival fibroblast proliferation. (A) Colony-forming unit cell morphology is represented by the colorization of Coomassie blue, while dECM without cell staining was used to distinguish between protein staining and the actual cell-forming colonies. (B) mRNA expression of GFs seeded on dECM at 48 h. Scale bars represent 1000 μm. The data are presented as the means ± standard errors (SEs). Statistical significance is denoted by bars, indicating a significant difference between groups (p < 0.05)