1. Academic Validation
  2. YTHDF1 enhances chondrogenic differentiation by activating the Wnt/β-catenin signaling pathway

YTHDF1 enhances chondrogenic differentiation by activating the Wnt/β-catenin signaling pathway

  • Stem Cells Dev. 2023 Jan 17. doi: 10.1089/scd.2022.0216.
Xiaoming Yang 1 Youxi Lin 2 Taiqiu Chen 3 Wenjun Hu 4 Pengfei Li 5 Xuemei Qiu 6 Bo Yang 7 Anjing Liang 8 Wenjie Gao 9
Affiliations

Affiliations

  • 1 Renmin Hospital of Wuhan University, 117921, Wuhan, Hubei , China; yangxm6@whu.edu.cn.
  • 2 Sun Yat-Sen Memorial Hospital, 56713, Guangzhou, Guangdong, China; Linuc5@126.com.
  • 3 Sun Yat-Sen Memorial Hospital, 56713, Guangzhou, Guangdong, China; chentq6@mail2.sysu.edu.cn.
  • 4 Sun Yat-Sen Memorial Hospital, 56713, Guangzhou, Guangdong, China; huwj9@mail2.sysu.edu.cn.
  • 5 Sun Yat-Sen Memorial Hospital, 56713, Guangzhou, Guangdong, China; pengfei_li0703@163.com.
  • 6 Sun Yat-Sen Memorial Hospital, 56713, Guangzhou, Guangdong, China; qiqi0214@126.com.
  • 7 Renmin Hospital of Wuhan University, 117921, Wuhan, Hubei , China; yangbo3399@whu.edu.cn.
  • 8 Sun Yat-Sen Memorial Hospital, 56713, Guangzhou, Guangdong, China; lianganj@mail.sysu.edu.cn.
  • 9 Sun Yat-Sen Memorial Hospital, 56713, Guangzhou, China, 510120; gaowj7@mail.sysu.edu.cn.
Abstract

Cartilage is derived from the chondrogenic differentiation of stem cells, for which the regulatory mechanism has not been fully elucidated. N6-methyladenosine (m6A) mRNA methylation is the most common posttranscriptional modification in eukaryotic mRNAs and is mediated by m6A regulators. However, whether m6A regulators play roles in chondrogenic differentiation is unknown. Herein, we aim to determine the role of a main m6A reader protein, YTH N6-methyladenosine RNA binding protein 1 (YTHDF1), in chondrogenic differentiation regulation. Western blotting assays found the expression of YTHDF1 increased during chondrogenic differentiation of human bone marrow mesenchymal stem cells (hBMSCs). The results of qPCR, western blotting, immunohistochemistry and Alcian blue staining revealed that overexpression of YTHDF1 increased cartilage matrix synthesis and the expression of chondrogenic markers when hBMSCs, ATDC5 cells, or C3H10T1/2 cells were induced to undergo chondrogenesis. Conversely, chondrogenesis was clearly inhibited when YTHDF1 was knocked down in hBMSCs, ATDC5 cells, or C3H10T1/2 cells. Further RNA Sequencing and Molecular Biology experiments found that YTHDF1 activated the Wnt/β-catenin signaling pathway during chondrogenic differentiation. Finally, the effects of overexpression and knockdown of YTHDF1 on chondrogenic differentiation were reversed by inhibiting or activating β-catenin activity. Therefore, we demonstrated that YTDHF1 promoted chondrogenic differentiation through activation of the Wnt/β-catenin signaling pathway.

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