Liao Yunyang, Fang Youran, Zhu Hanghang, Huang Yue, Zou Gengsen, Dai Bowen, Rausch Macro Aoqi, Shi Bin
Department of Oral and Maxillofacial Surgery, The First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
Laboratory of Facial Plastic and Reconstruction, Fujian Medical University, Fuzhou, China.
Front Bioeng Biotechnol. 2022 Mar 21;10:837295. doi: 10.3389/fbioe.2022.837295. eCollection 2022.
Osteogenesis is a complex physiologic process that occurs during bone regeneration. This process requires several growth factors that act on bone marrow-derived mesenchymal stem cells (BMSCs). Concentrated growth factor (CGF) is a new-generation platelet-rich derivative that is an appealing autologous material for application in tissue repair and bone regenerative medicine because it contains a variety of fibrin and growth factors. In this study, the effects of CGF on the proliferation and osteogenic differentiation of hBMSCs and human umbilical vein endothelial cells (HUVECs) were explored with cell co-culture experiments. HBMSCs and HUVECs were directly co-cultured at the ratio of 1:2 under different concentrations (0, 2, 5, 10, 20%) of CGF for 7 days. Alkaline phosphatase (ALP) staining and quantitative reverse transcription polymerase chain reaction were used to detect the effects of CGF on the expression of osteogenic genes (ALP, osteocalcin [OCN], type I collagen [COL-1], Runt-related transcription factor 2 [RUNX2]) and connexin 43 (CX43). RNA sequencing was used to explore potential regulated genes and signaling pathways that affect the osteogenesis of co-cultured hBMSCs exposed to CGF. The results showed higher expressions of ALP, COL-1, RUNX2, OCN, and CX43 in the direct co-culture group containing 10% CGF compared to the direct co-culture group without CGF and the indirect co-culture group. In summary, 10% CGF can significantly promote osteogenesis in hBMSCs directly co-cultured with HUVECs. Intercellular communication between the direct co-culture of hBMSCs and HUVECs through CX43 may be one of the main regulatory mechanisms.
骨生成是骨再生过程中发生的一个复杂生理过程。该过程需要多种作用于骨髓间充质干细胞(BMSCs)的生长因子。浓缩生长因子(CGF)是新一代富含血小板的衍生物,因其含有多种纤维蛋白和生长因子,是一种适用于组织修复和骨再生医学的有吸引力的自体材料。在本研究中,通过细胞共培养实验探讨了CGF对人BMSCs和人脐静脉内皮细胞(HUVECs)增殖和成骨分化的影响。将hBMSCs和HUVECs以1:2的比例在不同浓度(0、2、5、10、20%)的CGF下直接共培养7天。采用碱性磷酸酶(ALP)染色和定量逆转录聚合酶链反应检测CGF对成骨基因(ALP、骨钙素[OCN]、I型胶原[COL-1]、 runt相关转录因子2[RUNX2])和连接蛋白43(CX43)表达的影响。利用RNA测序探索影响暴露于CGF的共培养hBMSCs成骨的潜在调控基因和信号通路。结果显示,与无CGF的直接共培养组和间接共培养组相比,含10%CGF的直接共培养组中ALP、COL-1、RUNX2、OCN和CX43的表达更高。总之,10%CGF可显著促进与HUVECs直接共培养的hBMSCs的成骨作用。hBMSCs和HUVECs通过CX43直接共培养的细胞间通讯可能是主要调控机制之一。