Advanced Platelet-Rich Fibrin Extract Treatment Promotes the Proliferation and Differentiation of Human Adipose-Derived Mesenchymal Stem Cells through Activation of Tryptophan Metabolism

被引:2
|
作者
Lu, Guan-Ming [1 ]
Jiang, Li-Yuan [2 ]
Huang, Dong-Lin [3 ,4 ]
Rong, Yong-Xian [5 ]
Li, Yang-Hong [1 ]
Wei, Liu-Xing [1 ]
Ning, Yan [3 ,4 ]
Huang, Shan-Fu [6 ]
Mo, Steven [7 ]
Meng, Fu-Han [8 ]
Li, Hong-Mian [3 ,4 ]
机构
[1] Youjiang Med Univ Nationalities, Affiliated Hosp, Dept Breast & Thyroid Surg, Baise 533000, Guangxi, Peoples R China
[2] Guiping Peoples Hosp, Dept Orthopaed, Guigping 537200, Guangxi, Peoples R China
[3] Peoples Hosp Guangxi Zhuang Autonomous Reg, Res Ctr Med Sci, Nanning 530021, Peoples R China
[4] Guangxi Acad Med Sci, Nanning 530021, Peoples R China
[5] Guiping Peoples Hosp, Dept Burn & Plast Surg, Guigping 537200, Guangxi, Peoples R China
[6] Peoples Hosp Binyang Cty, Dept Dermatol, Binyang 530405, Guangxi, Peoples R China
[7] Yuan Dong Int Acad Life Sci, Nanning, Peoples R China
[8] Peoples Hosp Binyang Cty, Dept Rehabil Med, Binyang 530405, Guangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Adipose-derived Stem Cell; Advanced-platelet-rich Fibrin Extract; Proliferation; Differentiation; Pathway; Clinic; LONG NONCODING RNA; SIGNALING PATHWAY; EXPRESSION; TISSUE; MECHANISMS; DATABASE; NETWORK; AXIS;
D O I
10.2174/1574888X16666211206150934
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background: Advanced platelet-rich fibrin extract (APRFE) contains a high concentration of various cytokines that are helpful for improving stem cells repair function. Objective: However, the underlying mechanism of APRFE improving stem cell repairing is not clear. Methods: We produced APRFE by centrifuging fresh peripheral blood samples and isolated and identified human adipose-derived mesenchymal stem cells (ADMSCs). The abundance of cytokines contained in APRFE was detected by the Enzyme-linked immunosorbent assay (ELISA). The ADMSCs treated with or without APRFE were collected for transcriptome sequencing. Results: Based on the sequencing data, the expression profiles were contracted. The differentially expressed genes and lncRNA (DEGs and DElncRNAs) were obtained using for the differential expression analysis. The lncRNA-miRNA-mRNA network was constructed based on the miRNet database. The further enrichment analysis results showed that the biological functions were mainly related to proliferation, differentiation, and cell-cell function. To explore the role of APRFE, the protein-protein interaction network was constructed among the cytokines included in APRFE and DEGs. Furthermore, we constructed the global regulatory network based on the RNAInter and TR-RUST database. The pathways in the global regulatory network were considered as the core pathways. We found that the DEGs in the core pathways were associated with stemness scores. Conclusion: In summary, we predicted that APRFE activated three pathways (tryptophan metabolism, mTOR signaling pathway, and adipocytokine signaling) to promote the proliferation and differentiation of ADMSCs. The finding may be helpful for guiding the application of ADMSCs in the clinic.
引用
收藏
页码:127 / 142
页数:16
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