The First Affiliated Hospital, Zhejiang Chinese Medical University, Hangzhou, China.
Center for Stem Cell Translational Research, Zhejiang Chinese Medical University, Hangzhou, China.
Cell Death Dis. 2020 Oct 14;11(10):857. doi: 10.1038/s41419-020-03045-0.
Poor viability of mesenchymal stem cells (MSCs) at the transplanted site often hinders the efficacy of MSCs-based therapy. Platelet lysate (PL) contains rich amounts of growth factors, which benefits cell growth. This study aimed to explore how human PL benefits umbilical cord-derived MSCs (huc-MSCs), and whether they have synergistic potential in osteoarthritis (OA) treatment. As quality control, flow cytometry and specific staining were performed to identify huc-MSCs, and ELISA was used to quantify growth factors in PL. CCK-8 and flow cytometry assays were performed to evaluate the effects of PL on the cell viability and cell cycle progression of huc-MSCs. Wound healing and transwell assays were conducted to assess the migration of huc-MSCs. RNA sequencing, real time PCR, and Western blot assays were conducted to explore the growth factors-based mechanism of PL. The in vitro results showed that PL significantly promoted the proliferation, cell cycle, and migration of huc-MSCs by upregulating relevant genes/proteins and activating beclin1-dependent autophagy via the AMPK/mTOR signaling pathway. The main growth factors (PDGF-AA, IGF-1, TGF-β, EGF, and FGF) contributed to the effects of PL in varying degrees. The in vivo data showed that combined PL and huc-MSCs exerted significant synergistic effect against OA. The overall study determined the beneficial effects and mechanism of PL on huc-MSCs and indicated PL as an adjuvant for huc-MSCs in treating OA. This is the first report on the growth factors-based mechanism of PL on huc-MSCs and their synergistic application. It provides novel knowledge of PL's roles and offers a promising strategy for stem cell-based OA therapy by combining PL and huc-MSCs.
骨髓间充质干细胞(MSCs)在移植部位的存活率低往往会阻碍基于 MSCs 的治疗效果。血小板裂解液(PL)中含有丰富的生长因子,有利于细胞生长。本研究旨在探讨人 PL 对脐带间充质干细胞(huc-MSCs)的作用,以及它们在骨关节炎(OA)治疗中是否具有协同作用。作为质量控制,通过流式细胞术和特异性染色鉴定 huc-MSCs,通过 ELISA 定量 PL 中的生长因子。通过 CCK-8 和流式细胞术检测评估 PL 对 huc-MSCs 细胞活力和细胞周期进程的影响。通过划痕愈合和 Transwell 实验评估 huc-MSCs 的迁移。通过 RNA 测序、实时 PCR 和 Western blot 实验探讨 PL 基于生长因子的作用机制。体外实验结果表明,PL 通过上调相关基因/蛋白并激活 AMPK/mTOR 信号通路依赖性自噬,显著促进 huc-MSCs 的增殖、细胞周期和迁移。主要生长因子(PDGF-AA、IGF-1、TGF-β、EGF 和 FGF)在不同程度上对 PL 的作用有贡献。体内数据表明,PL 和 huc-MSCs 的联合应用对 OA 具有显著的协同作用。总的来说,本研究确定了 PL 对 huc-MSCs 的有益作用及其作用机制,并表明 PL 可作为 huc-MSCs 治疗 OA 的辅助剂。这是首次报道 PL 对 huc-MSCs 的基于生长因子的作用机制及其协同应用。它为 PL 的作用提供了新的认识,并通过联合 PL 和 huc-MSCs 为基于干细胞的 OA 治疗提供了有前景的策略。