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Correction: Enhancing osteogenic differentiation of MC3T3-E1 cells during inflammation using UPPE/β-TCP/TTC composites via the Wnt/β-catenin pathway
Qi-lin Liabc,
Ya-xin Wuabc,
Yu-xiao Zhangabc,
Jing Mao*abc and
Zhi-xing Zhang*abc
aDepartment of Stomatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China. E-mail: maojing@hust.edu.cn; zzx@tjh.tjmu.edu.cn
bSchool of Stomatology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China
cHubei Province Key Laboratory of Oral and Maxillofacial Development and Regeneration, Wuhan 430022, China
First published on 24th January 2024
Abstract
Correction for ‘Enhancing osteogenic differentiation of MC3T3-E1 cells during inflammation using UPPE/β-TCP/TTC composites via the Wnt/β-catenin pathway’ by Qi-lin Li et al., RSC Adv., 2024, 14, 1527–1537, https://doi.org/10.1039/D3RA05529A.
The authors regret that an incorrect version of Fig. 4 was included in the original article. The correct version of Fig. 4 is presented below.
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| Fig. 4 UPPE/β-TCP/TTC composites enhanced the osteogenic differentiation of MC3T3-E1 cells through the Wnt/β-catenin pathway under P.g-LPS stimulation. (a) Immunofluorescent staining of TOP-GFP and RUNX2 in MC3T3-E1 cells on the surface of UPPE/β-TCP and UPPE/β-TCP + 1% TTC after cell culture in P.g-LPS for 21 days. (b) The protein expression levels of β-catenin and p-β-catenin on the surface of UPPE/β-TCP and UPPE/β-TCP + 1% TTC after cell culture in P.g-LPS for 21 days. (c) Immunofluorescent staining of β-catenin in MC3T3-E1 cells on the surface of UPPE/β-TCP and UPPE/β-TCP + 1% TTC after cell culture in P.g-LPS for 21 days. (d) ARS and ALP staining of MC3T3-E1 cells (with or without JW67, the WNT pathway inhibitors) on the surface of UPPE/β-TCP + 1% TTC after cell culture in P.g-LPS for 21 days and quantitative analysis in (e) and (f). ***P < 0.001, ****P < 0.0001, compared with the without JW67 group. | ||
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