血管生成
干细胞
牙髓干细胞
间充质干细胞
牙周膜干细胞
趋化因子
细胞生物学
下调和上调
归巢(生物学)
内皮干细胞
伤口愈合
化学
癌症研究
免疫学
医学
生物
炎症
碱性磷酸酶
生物化学
体外
酶
基因
生态学
作者
Zhengrong Gao,Yinghui Zhou,Ya‐Qiong Zhao,Jie Zhao,Qin Ye,Shaohui Zhang,Yao Feng,Li Tan,Qiong Liu,Y. Chen,Ze-Yue Ou-Yang,Jiyi Hu,Marie Aimee Dusenge,Yun‐Zhi Feng,Yue Guo
摘要
Kangfuxin (KFX) shows potential in wound healing, but its role in socket healing is unclear. This research finds increased bone mass, mineralization, and collagen deposition in KFX-treated mice. Mouse bone marrow mesenchymal stem cells, human periodontal ligament stem cells (hPDLSCs), and human dental pulp stem cells (hDPSCs) are treated with KFX under osteogenic induction. RNA-sequencing reveals upregulated chemokine-related genes, with a threefold increase in chemokine (C-C motif) ligand 2 (Ccl2). The conditioned medium (CM) of hPDLSCs and hDPSCs treated with KFX promotes endothelial cell migration and angiogenesis. Ccl2 knockdown abolishes CM-induced endothelial cell migration and angiogenesis, which can be reversed by recombinant CCL2 treatment. KFX-treated mice showed increased vasculature. In conclusion, KFX increases the expression of CCL2 in stem cells, promoting bone formation and mineralization in the extraction socket by inducing endothelial cell angiogenesis. © 2023 American Society for Bone and Mineral Research (ASBMR).
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