Go Yoon-Young, Lee Chan-Mi, Chae Sung-Won, Song Jae-Jun
Department of Otorhinolaryngology-Head and Neck Surgery, Korea University Guro Hospital, 80 Guro-Dong, Guro-Gu, Seoul, 08308, South Korea.
Institute for Health Care Convergence Center, Korea University Guro Hospital, Seoul, 08308, Republic of Korea.
Biomater Res. 2023 Jun 27;27(1):62. doi: 10.1186/s40824-023-00396-5.
Human mesenchymal stem cells (MSCs) are therapeutic for clinical applications because of their excellent immunomodulatory and multiple lineage differentiation abilities at tissue injury sites. However, insufficient number of cells and lack of regenerative properties during in vitro expansion still limit the clinical applicability of MSC therapies. Here, we demonstrated a preconditioning strategy with trophoblast stem cell-derived extracellular vesicles (TSC-EVs) to boost the proliferation and regenerative capacity of MSCs.
We employed cell proliferation analyses such as CCK8 and BrdU assays to determine the proliferation-promoting role of TSC-EVs on MSCs. Osteogenic effects of TSC-EVs on MSCs were assessed by alkaline phosphatase (ALP) activity, calcium assays, and calvarial bone defect animal models. For skin regenerative effects, skin wound mice model was exploited to analyze wound-healing rate in this study, as well as immunofluorescence and histological staining evaluates. We also performed the small RNA profiling and RNA-sequencing analyzes to understand the cellular mechanism of TSC-EVs on MSCs.
TSC-EVs significantly promoted MSC proliferation under xeno-free conditions and facilitated the therapeutic effects of MSCs, including osteogenesis, anti-senescence, and wound healing. Transcriptomic analysis also provided evidence that specific microRNAs in TSC-EVs and differentially expressed genes (DEGs) in TSC-EV-treated MSCs showed the possibility of TSC-EVs triggering the regenerative abilities of MSCs with cytokine interaction. Hence, we found that NGF/Akt signaling mediated the regenerative effects of TSC-EVs on MSCs as a particular cellular signaling pathway.
The results of this study demonstrated the functional properties of TSC-EVs on MSCs for MSC-based therapeutic applications, suggesting that TSC-EVs may serve as a potential preconditioning source for MSC therapy in the clinical field of regenerative medicine.
人间充质干细胞(MSCs)因其在组织损伤部位具有出色的免疫调节和多谱系分化能力而适用于临床治疗。然而,体外扩增过程中细胞数量不足和缺乏再生特性仍然限制了MSC疗法的临床应用。在此,我们展示了一种用滋养层干细胞衍生的细胞外囊泡(TSC-EVs)进行预处理的策略,以提高MSCs的增殖和再生能力。
我们采用细胞增殖分析方法,如CCK8和BrdU检测,来确定TSC-EVs对MSCs的促增殖作用。通过碱性磷酸酶(ALP)活性、钙检测和颅骨缺损动物模型评估TSC-EVs对MSCs的成骨作用。对于皮肤再生作用,本研究利用皮肤创伤小鼠模型分析伤口愈合率,并进行免疫荧光和组织学染色评估。我们还进行了小RNA谱分析和RNA测序分析,以了解TSC-EVs对MSCs的细胞机制。
TSC-EVs在无血清条件下显著促进MSCs增殖,并促进MSCs的治疗效果,包括成骨、抗衰老和伤口愈合。转录组分析还提供了证据,表明TSC-EVs中的特定微小RNA和TSC-EV处理的MSCs中的差异表达基因(DEGs)显示了TSC-EVs通过细胞因子相互作用触发MSCs再生能力的可能性。因此,我们发现NGF/Akt信号通路作为一种特定的细胞信号通路介导了TSC-EVs对MSCs的再生作用。
本研究结果证明了TSC-EVs对基于MSCs的治疗应用的功能特性,表明TSC-EVs可能作为再生医学临床领域中MSC治疗的潜在预处理来源。