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Paulownin 通过激活 JNK 通路增强 NK 细胞细胞毒性产生抗肿瘤作用

英文原题:Paulownin elicits anti-tumor effects by enhancing NK cell cytotoxicity through JNK pathway activation.

查看英文原题

Paulownin elicits anti-tumor effects by enhancing NK cell cytotoxicity through JNK pathway activation.

PubMed 2024/09/04(内容时间) Front Pharmacol Q1 · IF 5.4(JCR 2025)

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中文摘要

Paulownin是一种从毛泡桐木材中提取的天然化合物,具有多种生理功能,包括抗细菌和抗真菌作用。然而,paulownin对自然杀伤(NK)细胞免疫活性的影响在很大程度上仍不清楚。

在本研究中,我们在体外和体内研究了paulownin对NK细胞活性的影响,并探讨了其潜在机制。NK-92细胞用于体外实验,皮下注射B16F10细胞的BALB/c小鼠模型用于体内抗肿瘤分析。

我们发现paulownin增强了NK-92细胞对白血病、人结肠癌和人肺癌细胞系的细胞溶解活性。Paulownin处理增加了NK-92细胞中脱颗粒标志蛋白CD107a以及细胞溶解颗粒(包括颗粒酶B和穿孔素)的表达。

此外,在人类原代NK细胞中也观察到paulownin诱导的这些细胞毒性增强和细胞溶解颗粒表达增加。信号传导研究表明,paulownin促进了JNK的磷酸化。通过JNK抑制剂预处理,paulownin诱导的穿孔素表达增加和细胞毒性活性升高被有效抑制。体内研究表明,给予paulownin抑制了同种移植到小鼠体内的B16F10黑色素瘤细胞的生长。Paulownin给药促进了小鼠脾脏中NK细胞的活化,从而增强了对YAC-1细胞的细胞毒性。

此外,在NK细胞耗竭后,paulownin的抗肿瘤作用减弱。因此,这些结果表明,paulownin通过激活JNK信号通路增强NK细胞毒性,并为开发癌症免疫治疗新策略提供了重要意义。

展开英文摘要原文

Paulownin, a natural compound derived from Paulownia tomentosa wood, exhibits various physiological functions, including anti-bacterial and anti-fungal effects.

However, the impact of paulownin on natural killer (NK) cell immune activity remains largely unknown. In this study, we investigated the effect of paulownin on NK cell activity both in vitro and in vivo , and explored its potential mechanisms. NK-92 cells were used for in vitro experiments and a BALB/c mouse model with B16F10 cells injected subcutaneously were used for in vivo anti-tumor analysis.

We found that paulownin enhanced the cytolytic activity of NK-92 cells against leukemia, human colon, and human lung cancer cell lines. Paulownin treatment increased the expression of the degranulation marker protein CD107a and cytolytic granules, including granzyme B and perforin in NK-92 cells.

Moreover, these enhancements of cytotoxicity and the expression of cytolytic granules induced by paulownin were also observed in human primary NK cells. Signaling studies showed that paulownin promoted the phosphorylation of JNK. The increased perforin expression and elevated cytotoxic activity induced by paulownin were effectively inhibited by pre-treatment with a JNK inhibitor.

In vivo studies demonstrated that the administration of paulownin suppressed the growth of B16F10 melanoma cells allografted into mice. Paulownin administration promoted the activation of NK cells in the spleen of mice, resulting in enhanced cytotoxicity against YAC-1 cells.

Moreover, the anti-tumor effects of paulownin were reduced upon the depletion of NK cells.

Therefore, these results suggest that paulownin enhances NK cell cytotoxicity by activating the JNK signaling pathway and provide significant implications for developing new strategies for cancer immunotherapy.

论文信息

作者
Park ES、Hwang YS、Ryu HW、Yoon HR、Kim JT、Lim JS、Cho HJ、Lee HG
单位
Immunotherapy Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.South Korea
期刊
Frontiers in pharmacology2024
原文标识
PubMed 39295927 · DOI 10.3389/fphar.2024.1439079