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논문 기본 정보

자료유형
학술저널
저자정보
Song Yameng (School and Hospital of Stomatology, Lanzhou University) Li Hongjiao (School and Hospital of Stomatology, Lanzhou University) Wang Zixuan (School and Hospital of Stomatology, Lanzhou University) Shi Jiamin (School of Life Sciences, Lanzhou University) Li Jing (School and Hospital of Stomatology, Lanzhou University) Wang Lu (School and Hospital of Stomatology, Lanzhou University) Liao Lingzi (School and Hospital of Stomatology, Lanzhou University) Ma Shengqin (School and Hospital of Stomatology, Lanzhou University) Zhang Yun (Lanzhou Hospital of Stomatology) Liu Bin (School and Hospital of Stomatology, Lanzhou University) Yang Yaling (Lanzhou Hospital of Stomatology) Zhou Ping (School and Hospital of Stomatology, Lanzhou University)
저널정보
한국조직공학과 재생의학회 조직공학과 재생의학 조직공학과 재생의학 제21권 제2호
발행연도
2024.2
수록면
291 - 308 (18page)
DOI
10.1007/s13770-023-00597-y

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Background: The addition of growth factiors is commonly applied to improve the osteogenic differentiation of stem cells. However, for human pluripotent stem cells (hPSCs), their complex differentiation processes result in the unknown effect at different stages. In this study, we focused on the widely used bone forming peptide-1 (BFP-1) and investigated the effect and mechanisms of its addition on the osteogenic induction of hPSCs as a function of the supplementation period. Methods: Monolayer-cultured hPSCs were cultured in osteogenic induction medium for 28 days, and the effect of BFP-1 peptide addition at varying weeks was examined. After differentiation for varying days (0, 7, 14, 21 and 28), the differentiation efficiency was determined by RT–PCR, flow cytometry, immunofluorescence, and alizarin red staining assays. Moreover, the expression of marker genes related to germ layers and epithelial-mesenchymal transition (EMT) was investigated at day 7. Results: Peptide treatment during the first week promoted the generation of mesoderm cells and mesenchymal-like cells from hiPSCs. Then, the upregulated expression of osteogenesis marker genes/proteins was detected in both hESCs and hiPSCs during subsequent inductions with BFP-1 peptide treatment. Fortunately, further experimental design confirmed that treating the BFP-1 peptide during 7–21 days showed even better performance for hESCs but was ineffective for hiPSCs. Conclusion: The differentiation efficiency of cells could be improved by determining the optimal treatment period. Our study has great value in maximizing the differentiation of hPSCs by adding osteogenesis peptides based on the revealed mechanisms and promoting the application of hPSCs in bone tissue regeneration.

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