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MiR-483-3p promotes dental pulp stem cells osteogenic differentiation via the MAPK signaling pathway by targeting ARRB2.
Yu, Xin; Ge, Juan; Xie, Huimin; Qian, Jialu; Xia, Wenqian; Wang, Qinghua; Zhou, Xiaorong; Zhou, Yan.
Affiliation
  • Yu X; Department of Orthodontics and Periodontology, Affiliated Nantong Stomatological Hospital of Nantong University, 36 South Yuelong Road, Nantong, 226001, China.
  • Ge J; Department of Immunology, School of Medicine, Nantong University, Nantong, China.
  • Xie H; Department of Orthodontics and Periodontology, Affiliated Nantong Stomatological Hospital of Nantong University, 36 South Yuelong Road, Nantong, 226001, China.
  • Qian J; Department of Clinical Laboratory, The First People's Hospital of Nantong, The Second Affiliated Hospital of Nantong University, Nantong, China.
  • Xia W; Department of Orthodontics and Periodontology, Affiliated Nantong Stomatological Hospital of Nantong University, 36 South Yuelong Road, Nantong, 226001, China.
  • Wang Q; Laboratory Animal Center, Nantong University, Nantong, China.
  • Zhou X; Department of Immunology, School of Medicine, Nantong University, Nantong, China. zhouxiaorong@ntu.edu.cn.
  • Zhou Y; Department of Orthodontics and Periodontology, Affiliated Nantong Stomatological Hospital of Nantong University, 36 South Yuelong Road, Nantong, 226001, China. ntyaner@126.com.
In Vitro Cell Dev Biol Anim ; 60(8): 879-887, 2024 Sep.
Article in En | MEDLINE | ID: mdl-38833209
ABSTRACT
Human dental pulp stem cells (DPSCs) have become an important component for bone tissue engineering and regenerative medicine due to their ability to differentiate into osteoblast precursors. Two miRNA chip datasets (GSE138180 and E-MTAB-3077) of DPSCs osteogenic differentiation were analyzed respectively to find the expression of miR-483-3p significantly increased in the differentiated groups. We further confirmed that miR-483-3p continued to overexpress during osteogenic differentiation of DPSCs, especially reaching its peak on the 7th day. Moreover, miR-483-3p could significantly promote the expression of osteogenic markers including RUNX2 and OSX, and activate MAPK signaling pathway by inducing phosphorylation of ERK, p38, and JNK. In addition, as a significant gene within the MAPK signaling pathway, ARRB2 was identified as the target gene of miR-483-3p by bioinformatic prediction and experimental verification. In conclusion, we identified miR-483-3p could promote osteogenic differentiation of DPSCs via the MAPK signaling pathway by targeting ARRB2.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteogenesis / Stem Cells / Cell Differentiation / MAP Kinase Signaling System / MicroRNAs / Dental Pulp Limits: Humans Language: En Journal: In Vitro Cell Dev Biol Anim Journal subject: BIOLOGIA Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteogenesis / Stem Cells / Cell Differentiation / MAP Kinase Signaling System / MicroRNAs / Dental Pulp Limits: Humans Language: En Journal: In Vitro Cell Dev Biol Anim Journal subject: BIOLOGIA Year: 2024 Document type: Article Affiliation country: Country of publication: