CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Migration Capacity of Stem Cells from Human Exfoliated Deciduous Teeth Towards Glioma.
Migration Capacity of Stem Cells from Human Exfoliated Deciduous Teeth Towards Glioma.
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我们的研究结果表明,SHED 有望用于追踪恶性胶质瘤。
人脱落乳牙来源干细胞(SHED)属于间充质干细胞,因增殖率高、多能性和免疫抑制特性,近期受到关注。然而,尚未研究过SHED的抗癌特性。因此,我们调查SHED能否用作治疗方式,特别是抗胶质瘤治疗。
体外研究中,我们评估SHED的运动能力,以及其向胶质瘤条件培养液和恶性胶质瘤分泌的特定生长因子迁移的能力。体内研究中,我们将SHED移植至裸鼠左侧大脑半球;这些小鼠此前已在右侧半球植入人恶性胶质瘤U87细胞。我们评估SHED是否具有致瘤潜能。
体外和体内实验均显示SHED向恶性胶质瘤迁移的能力较强。体外实验中,SHED向胶质瘤条件培养液及干细胞因子、血小板衍生生长因子BB、C-X-C基序趋化因子配体12和血管内皮生长因子等特定生长因子迁移。移植1周后,SHED聚集于对侧大脑半球的肿瘤细胞周围。此外,移植150天后,SHED仍存在于裸鼠脑内。最后,研究证实SHED未发生恶性转化,也未在小鼠脑内形成移植物生长。
研究结果表明,SHED有望用于追踪恶性胶质瘤。
Stem cells from human exfoliated deciduous teeth (SHED) are a mesenchymal stem cell type and have recently attracted attention for their high proliferative rate, multipotency, and immunosuppressive properties. However, SHED have not yet been investigated for anticancer properties. We therefore investigated whether SHED can be used as a treatment modality, particularly for anti-glioma therapy.
In vitro , we examined the mobility of SHED and their ability to migrate towards glioma-conditioned medium and specific growth factors secreted by malignant gliomas. In vivo , we transplanted SHED into the left hemisphere of nude mice that had been previously implanted with human malignant glioma U87 cells into the right hemisphere. We assessed whether SHED had tumorigenic potential.
SHED exhibited strong migration ability towards malignant glioma in both in vitro and in vivo assays. In vitro , SHED migrated towards glioma-conditioned medium and specific growth factors such as stem cell factor, platelet-derived growth factor BB, C-X-C motif chemokine ligand 12, and vascular endothelial growth factor. SHED were accumulated around tumor cells in the contralateral hemisphere 1 week after transplantation. Moreover, SHED remained in the brains of nude mice 150 days after transplantation. Finally, we verified that SHED had no malignant transformation or engraftment of SHED in the mouse brain.
Our findings indicate that SHED can potentially be applied to track malignant glioma.
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