首页|健脾养正方调控肿瘤相关巨噬细胞外泌体诱导胃癌细胞失巢凋亡的机制研究

健脾养正方调控肿瘤相关巨噬细胞外泌体诱导胃癌细胞失巢凋亡的机制研究

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目的 探讨健脾养正方调控肿瘤相关巨噬细胞(TAM)外泌体对胃癌失巢凋亡的影响及其机制.方法 体外诱导人单核细胞THP-1 建立TAM模型;超速离心法提取M0、TAM及TAM+健脾养正方外泌体,与胃癌细胞共孵育.流式细胞术检测各组外泌体对胃癌细胞失巢凋亡的影响.构建BALB/c移植瘤小鼠模型,Western blot检测移植瘤中凋亡蛋白的表达水平.Label-free质谱蛋白组学及生物信息学分析干预前后胃癌细胞中的差异蛋白;Western blot及qPCR实验检测差异蛋白异柠檬酸脱氢酶 1(IDH1)表达水平,泛素化实验检测IDH1 的泛素化水平;试剂盒检测α-酮戊二酸(α-KG)、NADPH/NADP+、谷胱甘肽(GSH/GSSG)水平及活性氧(ROS)含量.结果 TAM外泌体干预胃癌细胞后其失巢凋亡率降低(P<0.05,P<0.01);而TAM+健脾养正外泌体干预后则显著升高(P<0.05,P<0.01).小鼠体内实验中,TAM外泌体组瘤体内Cleaved Caspase-3/Caspase-3 的比值降低(P<0.05),而TAM+健脾养正方外泌体干预后比值明显增高(P<0.05).蛋白组学分析显示IDH1 在干预前后差异明显,且与三羧酸循环代谢相关.相较于M0 组,TAM组外泌体干预的胃癌细胞IDH1 泛素化水平升高,α-KG、NADPH/NADP+及GSH/GSSG水平明显增加,ROS含量降低(P<0.05),而TAM+健脾养正外泌体则可逆转上述现象.结论 健脾养正方通过调控TAM外泌体使胃癌细胞IDH1 发生泛素降解,降低胃癌细胞三羧酸循环代谢水平,促进ROS积累,诱发胃癌失巢凋亡,进而抑制胃癌发展.
Study on the Mechanism of Jianpi Yangzheng Formula Regulating Tumor-Associated Macrophage Exosomes to Induce Anoikis in Gastric Cancer Cells
OBJECTIVE To investigate the effect of Jianpi Yangzheng(JPYZ)formula regulating tumor-associated macrophage(TAM)exosomes on anoikis in gastric cancer and its mechanism.METHODS TAM model was established by inducing human mononuclear THP-1 cells in vitro;M0,TAM and TAM+JPYZ formula exosomes were extracted by ultracentrifugation and co-incuba-ted with gastric cancer cells.Flow cytometry was used to detect the effect of exosomes in each group on anoikis in gastric cancer cells.A BALB/c transplanted tumor mouse model was constructed,and the expression level of apoptotic proteins in transplanted tumors was detected by Western blot.Label-free mass spectrometry proteomics and bioinformatics were used to analyze the differential proteins in gastric cancer cells before and after intervention;Western blot and qPCR experiments were used to detect the expression level of dif-ferential protein isocitrate dehydrogenase 1(IDH1),and ubiquitination experiments were used to detect the ubiquitination level of IDH1;kits were used to detect the levels of α-ketoglutarate(α-KG),NADPH/NADP+,glutathione(GSH/GSSG)and reactive oxy-gen species(ROS)content.RESULTS The anoikis rate of gastric cancer cells was reduced after TAM exosomes intervention(P<0.05,P<0.01),while it was significantly increased after TAM+JPYZ exosomes intervention(P<0.05,P<0.01).In the in vivo mouse experiment,the ratio of Cleaved Caspase-3/Caspase-3 in the tumor of the TAM exosome group was reduced(P<0.05),while the ra-tio was significantly increased after TAM+JPYZ exosome intervention(P<0.05).Proteomic analysis showed that IDH1 was significant-ly different after intervention,and was related to tricarboxylic acid cycle metabolism.Compared with the M0 group,the IDH1 ubiquiti-nation level of gastric cancer cells in the TAM group with exosome intervention was increased,the levels of α-KG,NADPH/NADP+and GSH/GSSG were significantly increased,and the ROS content was reduced(P<0.05),while TAM+JPYZ exosomes could reverse the above phenomenon.CONCLUSION JPYZ Formula can regulate TAM exosomes to cause ubiquitin degradation of IDH1 in gas-tric cancer cells,reduce the level of tricarboxylic acid cycle metabolism in gastric cancer cells,promote ROS accumulation,induce anoikis in gastric cancer,and thus inhibit the development of gastric cancer.

gastric cancerexosometumor-associated macrophageIDH1anoikisCaspase-3tricarboxylic acid cycle metabo-lism

郑姗姗、吴坚、张瑞娟、张翔、郑晓霞、卢雨佳、黄磊、孙庆敏

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南京中医药大学附属医院,江苏 南京 210029

南京中医药大学第一临床医学院,江苏 南京 210023

南京市浦口区中医院,江苏 南京 210000

胃癌 外泌体 肿瘤相关巨噬细胞 IDH1 失巢凋亡 Caspase-3 三羧酸循环代谢

国家自然科学基金面上项目国家自然科学基金面上项目江苏省自然科学基金面上项目江苏省研究生科研与实践创新计划项目江苏省研究生科研与实践创新计划项目江苏省中医院院级课题江苏省中医药管理局课题江苏省中医药管理局课题

8217419782374274BK20211392KYCX24_2246SJCX24_092720085-9-7JD2022SZ06JD2023SZ19

2024

南京中医药大学学报
南京中医药大学

南京中医药大学学报

CSTPCD北大核心
影响因子:1.658
ISSN:1672-0482
年,卷(期):2024.40(9)
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