METTL3 Promotes Osteogenic Differentiation of Human Periodontal Ligament Stem Cells through IGF2BP1-Mediated Regulation of Runx2 Stability
Xuefei Sun, Xiujiao Meng, Y. Piao, Shaojie Dong, Qianqian Dong
Abstract
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Xuefei Sun, Xiujiao Meng, Y. Piao, Shaojie Dong, Qianqian Dong
Abstract
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N6-Methyladenosine (m 6 A) has been reported to play a dynamic role in osteoporosis and bone metabolism.However, whether m 6 A is involved in the osteogenic differentiation of human periodontal ligament stem cells (hPDLSCs) remains unclear.Here, we found that methyltransferase-like 3 (METTL3) was up-regulated synchronously with m 6 A during the osteogenic differentiation of hPDLSCs.Functionally, lentivirus-mediated knockdown of METTL3 in hPDLSCs impaired osteogenic potential.Mechanistic analysis further showed that METTL3 knockdown decreased m 6 A methylation and reduced IGF2BP1-mediated stability of runt-related transcription factor 2 (Runx2) mRNA, which in turn inhibited osteogenic differentiation.Therefore, METTL3-based m 6 A modification favored osteogenic differentiation of hPDLSCs through IGF2BP1-mediated Runx2 mRNA stability.Our study shed light on the critical roles of m 6 A on regulation of osteogenic differentiation in hPDLSCs and served novel therapeutic approaches in vital periodontitis therapy.
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N6-Methyladenosine (m 6 A) has been reported to play a dynamic role in osteoporosis and bone metabolism.However, whether m 6 A is involved in the osteogenic differentiation of human periodontal ligament stem cells (hPDLSCs) remains unclear.Here, we found that methyltransferase-like 3 (METTL3) was up-regulated synchronously with m 6 A during the osteogenic differentiation of hPDLSCs.Functionally, lentivirus-mediated knockdown of METTL3 in hPDLSCs impaired osteogenic potential.Mechanistic analysis further showed that METTL3 knockdown decreased m 6 A methylation and reduced IGF2BP1-mediated stability of runt-related transcription factor 2 (Runx2) mRNA, which in turn inhibited osteogenic differentiation.Therefore, METTL3-based m 6 A modification favored osteogenic differentiation of hPDLSCs through IGF2BP1-mediated Runx2 mRNA stability.Our study shed light on the critical roles of m 6 A on regulation of osteogenic differentiation in hPDLSCs and served novel therapeutic approaches in vital periodontitis therapy.
Key concepts: Periodontal ligament stem cells, RUNX2, Gene knockdown, Cell biology, Periodontal fiber, Stem cell, Cellular differentiation, Transcription factor