首页|褪黑素通过自噬途径降低卵巢癌细胞表面PD-L1表达促进T细胞对肿瘤细胞的杀伤作用

褪黑素通过自噬途径降低卵巢癌细胞表面PD-L1表达促进T细胞对肿瘤细胞的杀伤作用

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目的:探讨褪黑素对卵巢癌细胞表面PD-L1表达的影响.方法:褪黑素作用于卵巢癌细胞OVCAR3,流式细胞术检测不同处理后卵巢癌细胞表面PD-L1表达水平,Western blot检测不同处理后卵巢癌细胞中PD-L1及LC-3的表达,加入自噬抑制剂Autophinib后,流式细胞术检测卵巢癌细胞表面PD-L1表达,卵巢癌细胞经褪黑素处理或褪黑素和自噬抑制剂共同处理后与人T淋巴细胞Jurkat共孵育,流式细胞术检测卵巢癌细胞凋亡比例.结果:褪黑素处理显著降低了卵巢癌细胞表面PD-L1表达,促进了卵巢癌细胞的自噬,自噬抑制剂能够逆转褪黑素下调的PD-L1表达,Jurkat细胞杀伤更多褪黑素处理后的卵巢癌细胞,自噬抑制剂能够逆转Jurkat细胞对卵巢癌细胞的杀伤.结论:褪黑素能够增强T细胞对卵巢癌细胞的杀伤.
Melatonin promotes killing effect of T cells on ovarian cancer cells by reduces expression of PD-L1 on surface of cancer cells via autophagy pathway
Objective:To investigate the effect of melatonin on the expression of PD-L1 on the surface of ovarian cancer cells.Methods:Ovarian cancer cell line OVCAR3 was treated with melatonin,then flow cytometry was used to detect the expression level of PD-L1 on the surface of ovarian cancer cells.Western blot was used to detect the expressions of PD-L1 and LC-3 in ovarian cancer cells after different treatments.After adding autophagy inhibitor Autophinib,flow cytometry was used to detect the expression of PD-L1 on the surface of ovarian cancer cells,ovarian cancer cells were treated with melatonin or melatonin combined with autophagy inhibi-tors and co-incubated with human T lymphocyte Jurkat.The proportion of ovarian cancer cell apoptosis was detected by flow cytometry.Results:Melatonin treatment significantly reduced expression of PD-L1 on the surface of ovarian cancer cells,promoted autophagy of ovar-ian cancer cells.Autophagy inhibitors reversed down regulation of PD-L1 treated by melatonin,Jurkat cells killed more melatonin treated ovarian cancer cells,and the killing of ovarian cancer cells by Jurkat cells revised by autophagy inhibitors.Conclusion:Mela-tonin can enhance the killing effect of T cells on ovarian cancer cells.

MelatoninAutophagyOvarian cancerPD-L1

张海光、华方方、崔非非、林志强、杨君

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新乡医学院第一附属医院,新乡 453100

褪黑素 自噬 卵巢癌 PD-L1

河南省医学科技攻关计划

LHGJ20200498

2024

中国免疫学杂志
中国免疫学会,吉林省医学期刊社

中国免疫学杂志

CSTPCD北大核心
影响因子:0.926
ISSN:1000-484X
年,卷(期):2024.40(5)
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