Zhai Shafei, Liu Changkui, Vimalraj Selvaraj, Subramanian Raghunandhakumar, Abullais Shahabe Saquib, Arora Suraj, Saravanan Sekaran
Department of Stomatology, Xi'an Medical University, Xi'an 710021, Shaanxi, China; Department of Periodontology, Hospital of Stomatology, The Third Affiliated Hospital of Xi'an Medical University, Xi'an 710068, Shaanxi, China.
Center for Biotechnology, Anna University, Chennai 600025, India; Department of Prosthodontics, Saveetha Dental College and Hospital, Saveetha Institute of Medical and Technical Sciences, SIMATS, Chennai 600077, Tamil Nadu, India.
Peptides. 2023 May;163:170974. doi: 10.1016/j.peptides.2023.170974. Epub 2023 Feb 11.
Bone cells express the glucagon-like peptide 1 receptor (GLP-1R). However, its presence and role in human dental pulp derived stem cells (hDPSCs) remains elusive. Hence, in the current study, we isolated hDPSCs and differentiated them into osteoblasts, where GLP-1R expression was found to be upregulated during osteoblast differentiation. GLP-1 receptor agonist, liraglutide peptide treatment, increased osteoblast differentiation in hDPSCs by increasing calcium deposition, ALP activity, and osteoblast marker genes, Runx2, type 1 col, osteonectin, and osteocalcin. Furthermore, activation of long non-coding RNA (LncRNA) LINC00968 and microRNA-3658 signalling increased Runx2 expression. Specifically, liraglutide increased LncRNA-LINC00968 expression while decreasing miR-3658 expression. LINC00968 targets miR-3658, and miR-3658 targets Runx2. Additionally, in an in-vivo study, zebrafish scale regeneration model, liraglutide promoted calcium deposition, osteoblastic cell count, collagen 1α, osteonectin, osteocalcin, runx2a MASNA isoform expression (transcribed from promoter P1), and Ca/P ratio in scales. Overall, GLP-1R activation promotes osteoblast differentiation via Runx2/LncRNA-LINC00968/miR-3658 signalling in hDPSCs and promotes bone formation in zebrafish scale regeneration.
骨细胞表达胰高血糖素样肽1受体(GLP-1R)。然而,其在人牙髓来源干细胞(hDPSC)中的存在及作用仍不清楚。因此,在本研究中,我们分离了hDPSC并将其分化为成骨细胞,发现在成骨细胞分化过程中GLP-1R表达上调。GLP-1受体激动剂利拉鲁肽肽处理通过增加钙沉积、碱性磷酸酶(ALP)活性以及成骨细胞标记基因Runx2、I型胶原、骨连接蛋白和骨钙素,促进了hDPSC中的成骨细胞分化。此外,长链非编码RNA(LncRNA)LINC00968和微小RNA-3658信号通路的激活增加了Runx2的表达。具体而言,利拉鲁肽增加了LncRNA-LINC00968的表达,同时降低了miR-3658的表达。LINC00968靶向miR-3658,而miR-3658靶向Runx2。此外,在一项体内研究即斑马鱼鳞片再生模型中,利拉鲁肽促进了钙沉积、成骨细胞计数、I型胶原、骨连接蛋白、骨钙素、runx2a MASNA亚型表达(从启动子P1转录)以及鳞片中的钙磷比。总体而言,GLP-1R激活通过hDPSC中的Runx2/LncRNA-LINC00968/miR-3658信号通路促进成骨细胞分化,并促进斑马鱼鳞片再生中的骨形成。