间充质干细胞
体内
癌症研究
牙周膜干细胞
体外
药物输送
趋化因子受体
化学
趋化因子
干细胞
细胞
牙髓干细胞
材料科学
趋化因子受体
受体
纳米技术
细胞生物学
医学
病理
生物
生物化学
生物技术
碱性磷酸酶
酶
作者
Dabo Zhou,Yixin Chen,Wenhuan Bu,Lin Meng,Congcong Wang,Nianqiang Jin,Yumeng Chen,Chun‐Xia Ren,Kai Zhang,Hongchen Sun
标识
DOI:10.1016/j.jcis.2021.05.126
摘要
Engineering a targetable nanoparticle to tumor cell is a challenge issue for clinical application. Our results demonstrated that the chemokine CXCL8 secreted by oral squamous cell carcinoma (OSCC) could act as a chemoattractant to attract dental pulp mesenchymal stem cell (DPSC), which expressed the CXCL8 binding receptor, CXCR2, to the OSCC. Therefore, to create OSCC targetable nanoparticles, we used DPSC membranes to modify nanoparticles of metal-organic framework nanoparticles (MOFs) resulting in a novel [email protected] nanoparticle. Interestingly, results from in vitro and in vivo experiments illustrated that [email protected] possessed specificity for the OSCC, and the [email protected] carried DOX (doxorubicin), [email protected] could induce CAL27 cell death in vitro and block CAL27 tumor growth in vivo. Our data suggest that this novel [email protected] nanoparticle is a potential targetable drug delivery system for the OSCC in the future clinical application.
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