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胰高血糖素样肽-1受体在斑马鱼鳞片再生模型中促进牙髓干细胞的成骨细胞分化和骨形成。

Glucagon-like peptide-1 receptor promotes osteoblast differentiation of dental pulp stem cells and bone formation in a zebrafish scale regeneration model.

作者信息

Zhai Shafei, Liu Changkui, Vimalraj Selvaraj, Subramanian Raghunandhakumar, Abullais Shahabe Saquib, Arora Suraj, Saravanan Sekaran

机构信息

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.

出版信息

Peptides. 2023 May;163:170974. doi: 10.1016/j.peptides.2023.170974. Epub 2023 Feb 11.

Abstract

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.

摘要

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。

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