Effect of circular RNA hsa_circ_0008016 on the Osteogenic and Odontogenic Ability of Stem Cells from Apical Papilla

DOI Web Site 37 References
  • Xu Jiali
    Department of Stomatology, The Affiliated Changzhou No.2 People’s Hospital of Nanjing Medical University, Changzhou Medical Center of Nanjing Medical University
  • Han Xuan
    Department of Stomatology, Cancer Hospital Chinese Academy of Medical Science
  • Yang Haibing
    Department of Stomatology, The Affiliated Changzhou No.2 People’s Hospital of Nanjing Medical University, Changzhou Medical Center of Nanjing Medical University
  • He Lei
    Department of Stomatology, The Affiliated Changzhou No.2 People’s Hospital of Nanjing Medical University, Changzhou Medical Center of Nanjing Medical University
  • Wang Yan
    Department of VIP center, School and Hospital of Stomatology, Shandong University & Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration
  • Tian Juzhong
    Department of Stomatology, The Affiliated Changzhou No.2 People’s Hospital of Nanjing Medical University, Changzhou Medical Center of Nanjing Medical University

Abstract

<p>This research aims to explore the role of hsa_circ_0008016 in osteogenic (OS) and odontogenic (OD) differentiation of stem cells derived from the apical papilla (SCAPs). SCAPs were isolated and cultured in either growth medium or OS and OD medium. RNA extraction was performed, followed by RNA sequencing to identify the circular RNA (circRNA) that exhibited the most significant changes between non-induced SCAPs and OS and OD-induced SCAPs, namely, hsa_circ_0008016. Subsequently, the over-expression vector pLenti-CMV-Hsa_circ_0008016-GFP-Puro was transfected into SCAPs, and the OS and OD ability of SCAPs was determined through qRT-PCR and Western blotting. In addition, the impact of hsa_circ_0008016 on 19 miRNAs were studied. Following the upregulation of hsa_circ_0008016 expression, qRT-PCR and Western blot analyses showed the expression of miRNA-660-5p, miRNA-337-3p, miRNA-376a-3p, miRNA-22-5p, bone sialoprotein (BSP) and dentin matrix protein 1 (DMP1), were increased, while the expression levels of collagenase I (COL1) and dentin sialophosphoprotein (DSPP) were decreased significantly. The target gene of miRNA-337-3p and hsa_circ_0008016 was predicted to be fibroblast growth factor receptor 1 (FGFR1). This study reveals that the hsa_circ_0008016 may enhance OS differentiation, while diminishing OD differentiation in SCAPs. This effect is likely mediated through hsa_circ_0008016 and miRNA-337-3p, potentially influencing the fibroblast growth factor (FGF)/fibroblast growth factor receptor (FGFR) signaling pathway, which warrants further validation.</p>

Journal

References(37)*help

See more

Keywords

Details 詳細情報について

Report a problem

Back to top