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新型吲哚二酮衍生物诱导肿瘤细胞免疫死亡的细胞机制。

Cellular Mechanism of Newly Synthesized Indoledione Derivative-induced Immunological Death of Tumor Cell.

机构信息

Office of Biomedical Science, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 135-710, Korea.

出版信息

Immune Netw. 2011 Dec;11(6):383-9. doi: 10.4110/in.2011.11.6.383. Epub 2011 Dec 31.

DOI:10.4110/in.2011.11.6.383
PMID:22346779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3275708/
Abstract

BACKGROUND

EY-6 is one of the newly synthesized indoledione derivatives to induce tumor cell-specific cell death. In this study, we investigated the mechanism of immunological death induced by EY-6 at mouse colon cancer cell as well as at the normal immune cell represented by dendritic cell.

METHODS

C57BL/6 mouse syngeneic colon cancer cell MC38 was treated with EY-6, and analyzed by MTT for viability test, flow cytometry for confirming surface expressing molecules and ELISA for detection of cytokine secretion. Normal myeloid-dendritic cell (DC) was ex vivo cultured from bone marrow hematopoietic stem cells of C57BL/6 mice with GM-CSF and IL-4 to analyze the DC uptake of dead tumor cells and to observe the effect of EY-6 on the normal DC.

RESULTS

EY-6 killed the MC38 tumor cells in a dose dependent manner (25, 50 and 100 µM) with carleticulin induction. And EY-6 induced the secretion of IFN-γ but not of TNF-α from the MC38 tumor cells. EY-6 did not kill the ex-vivo cultured DCs at the dose killing tumor cells and did slightly but not significantly induced the DC maturation. The OVA-specific cross-presentation ability of DC was not induced by chemical treatment (both MHC II and MHC I-restricted antigen presentation).

CONCLUSION

Data indicate that the EY-6 induced tumor cell specific and immunological cell death by modulation of tumor cell phenotype and cytokine secretion favoring induction of specific immunity eliminating tumor cells.

摘要

背景

EY-6 是一种新合成的吲哚二酮衍生物,可诱导肿瘤细胞特异性细胞死亡。在本研究中,我们研究了 EY-6 在小鼠结肠癌细胞以及树突状细胞(代表正常免疫细胞)中诱导免疫死亡的机制。

方法

用 EY-6 处理 C57BL/6 小鼠同基因结肠癌细胞 MC38,通过 MTT 进行活力试验、流式细胞术确认表面表达分子和 ELISA 检测细胞因子分泌进行分析。从 C57BL/6 小鼠的骨髓造血干细胞中用 GM-CSF 和 IL-4 体外培养正常髓样树突状细胞(DC),分析 DC 对死亡肿瘤细胞的摄取,并观察 EY-6 对正常 DC 的影响。

结果

EY-6 以剂量依赖性方式(25、50 和 100 µM)诱导姜黄素诱导的 MC38 肿瘤细胞死亡。并且 EY-6 诱导 MC38 肿瘤细胞分泌 IFN-γ,但不分泌 TNF-α。在杀死肿瘤细胞的剂量下,EY-6 不会杀死体外培养的 DC,并且轻微但不显著地诱导 DC 成熟。化学处理(MHC II 和 MHC I 限制性抗原呈递)不会诱导 DC 的 OVA 特异性交叉呈递能力。

结论

数据表明,EY-6 通过调节肿瘤细胞表型和细胞因子分泌诱导肿瘤细胞特异性和免疫细胞死亡,有利于诱导特异性免疫消除肿瘤细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/0aa4247d5737/in-11-383-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/694575a74051/in-11-383-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/76e31f12b2d1/in-11-383-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/aca55faf0d87/in-11-383-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/905ce87c15c0/in-11-383-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/bb761508faad/in-11-383-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/0aa4247d5737/in-11-383-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/694575a74051/in-11-383-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/76e31f12b2d1/in-11-383-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/aca55faf0d87/in-11-383-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/905ce87c15c0/in-11-383-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/bb761508faad/in-11-383-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe6/3275708/0aa4247d5737/in-11-383-g006.jpg

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