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通过脂质体-微泡复合物超声控制释放阿霉素诱导增强的免疫原性细胞死亡

Induction of enhanced immunogenic cell death through ultrasound-controlled release of doxorubicin by liposome-microbubble complexes.

作者信息

Huang Feng-Ying, Lei Jing, Sun Yan, Yan Fei, Chen Bin, Zhang Liming, Lu Zhuoxuan, Cao Rong, Lin Ying-Ying, Wang Cai-Chun, Tan Guang-Hong

机构信息

Key Laboratory of Tropical Diseases and Translational Medicine of the Ministry of Education & Hainan Provincial Key Laboratory of Tropical Medicine, Hainan Medical College, Haikou , China.

Department of Respiratory Medicine, The First Affiliated Hospital of Hainan Medical College, Haikou , China.

出版信息

Oncoimmunology. 2018 Mar 26;7(7):e1446720. doi: 10.1080/2162402X.2018.1446720. eCollection 2018.

Abstract

Immunogenic cell death (ICD) is a specific kind of cell death that stimulates the immune system to combat cancer cells. Ultrasound (US)-controlled targeted release of drugs by liposome-microbubble complexes is a promising approach due to its non-invasive nature and visibility through ultrasound imaging. However, it is not known whether this approach can enhance ICD induced by drugs, such as doxorubicin. Herein, we prepared a doxorubicin-liposome-microbubble complex (MbDox), and the resultant MbDox was then characterized and tested for US-controlled release of Dox (MbDox+US treatment) to enhance the induction of ICD in LL/2 and CT26 cancer cells and in syngeneic murine models. We found that MbDox+US treatment caused more cellular uptake and nuclear accumulation of Dox in tumor cells, and more accumulation of Dox in tumor tissues. Enhanced induction of ICD occurred both and . MbDox+US treatment induced more apoptosis, stronger membrane exposure and the release of ER stress proteins and DAMPs in tumor cells, and increased DC maturation . In addition, MbDox+US treatment also resulted in stronger therapeutic effects in immunocompetent mice than in immunodeficient mice. Moreover, MbDox+US enhancement of ICD was also evidenced by a higher proportion of activated CD8 T-lymphocytes but lower Treg in tumor tissues. Taken together, our results demonstrate that US-controlled release of ICD inducers into nuclei using liposome-microbubble complexes may be an effective approach to enhance the induction of ICD for tumor treatment.

摘要

免疫原性细胞死亡(ICD)是一种特定类型的细胞死亡,可刺激免疫系统对抗癌细胞。脂质体-微泡复合物在超声(US)控制下靶向释放药物是一种很有前景的方法,因为它具有非侵入性且可通过超声成像观察。然而,尚不清楚这种方法是否能增强由多柔比星等药物诱导的ICD。在此,我们制备了多柔比星-脂质体-微泡复合物(MbDox),然后对所得的MbDox进行表征,并测试其在超声控制下释放多柔比星(MbDox+US处理),以增强LL/2和CT26癌细胞以及同基因小鼠模型中ICD的诱导。我们发现MbDox+US处理导致肿瘤细胞中多柔比星的细胞摄取和核积累增加,以及肿瘤组织中多柔比星的积累增加。ICD的诱导增强在……均有发生。MbDox+US处理诱导肿瘤细胞中更多的细胞凋亡、更强的膜暴露以及内质网应激蛋白和损伤相关分子模式(DAMP)的释放,并增加树突状细胞(DC)成熟。此外,MbDox+US处理在免疫健全小鼠中比在免疫缺陷小鼠中产生更强的治疗效果。而且,肿瘤组织中活化的CD8 T淋巴细胞比例更高但调节性T细胞(Treg)更低也证明了MbDox+US对ICD的增强作用。综上所述,我们的结果表明,使用脂质体-微泡复合物在超声控制下将ICD诱导剂释放到细胞核中可能是增强ICD诱导用于肿瘤治疗的有效方法。

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