[miR-373通过调控JAK2/STAT6信号通路抑制肿瘤相关巨噬细胞M2极化,影响直肠癌细胞]。

细胞与分子免疫学杂志 Pub Date : 2025-03-01
Zhi Li, Di Wu, Xingming Xie, Fei Tian, Jie Liu
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TAM were transfected and divided into overexpressing miR-373 group (miR-373-TAM) and control group (miR-NC-TAM), overexpressing miR-373+JAK2-TAM group (miR-373 combined with JAK2-TAM) and control group (miR-373 combined with NC-TAM), and then cocultured with Caco-2 cells. Flow cytometry was used to detect the expression of CD206 in TAM; Real-time quantitative PCR and Western blot were used to detect miR-373, Arg1, Ym1, Fizz1, IL-10, JAK2, STAT6 mRNA and protein levels in TAM; CCK-8 assay, colony formation assay, and Transwell assay were used to detect the proliferation, migration, and invasion ability of Caco-2 cells. Thirty nude mice were randomly divided into Caco-2 cells group, Caco-2 cells combined with miR-NC-TAM group, and Caco-2 cells combined with miR-373-TAM group, with 10 mice in each group. Rats in each group were subcutaneously injected with pure Caco-2 cells, Caco-2 cells combined with TAM, and Caco-2 cells combined with TAM overexpressing miR-373. 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引用次数: 0

摘要

目的探讨miR-373和Janus kinase 2/signal transducer and activator of transcription 6 (JAK2/STAT6)信号通路对直肠癌肿瘤相关巨噬细胞(tumor associated macrophages, TAM) M2极化的影响。方法将THP-1细胞诱导为M0/M1/M2巨噬细胞,M0巨噬细胞与Caco-2细胞共培养获得TAM,流式细胞术检测CD86和CD206的表达,Real-time定量qPCR和Western blot检测miR-373、诱导型一氧化氮合酶(iNOS)、toll样受体4 (TLR-4)、白细胞介素1β (IL-1β)、肿瘤坏死因子α (TNF-α)、精氨酸酶1 (Arg1)、几次质酶3样1 (Ym1)、抵抗素样α (Fizz1)、IL-10 mRNA和蛋白水平。转染TAM后分为过表达miR-373组(miR-373-TAM)和对照组(miR-NC-TAM),过表达miR-373+JAK2-TAM组(miR-373联合JAK2-TAM)和对照组(miR-373联合NC-TAM),然后与Caco-2细胞共培养。流式细胞术检测TAM中CD206的表达;采用Real-time定量PCR和Western blot检测TAM组织中miR-373、Arg1、Ym1、Fizz1、IL-10、JAK2、STAT6 mRNA及蛋白水平;CCK-8法、集落形成法和Transwell法检测Caco-2细胞的增殖、迁移和侵袭能力。将30只裸鼠随机分为Caco-2细胞组、Caco-2细胞联合miR-NC-TAM组和Caco-2细胞联合miR-373-TAM组,每组10只。各组大鼠皮下注射纯Caco-2细胞、Caco-2细胞联合TAM、Caco-2细胞联合过表达miR-373的TAM。细胞接种4周后,采用免疫荧光染色法检测肿瘤组织中F4/80+CD206+细胞水平;采用实时荧光定量PCR和Western blot检测肿瘤组织中miR-373、JAK2、STAT6、Arg1、Ym1、Fizz1、IL-10 mRNA及蛋白水平。结果TAM倾向于M2极化。过表达miR-373后,TAM中miR-373水平升高,而Arg1、Ym1、Fizz1、IL-10、JAK2、STAT6 mRNA及蛋白水平降低,Caco-2细胞的增殖、迁移、侵袭能力降低;JAK2过表达可部分逆转miR-373过表达对TAM M2极化及Caco-2细胞增殖、迁移、侵袭能力的影响。TAM能促进肿瘤生长;过表达miR-373可抑制肿瘤生长,抑制TAM的M2极化。结论miR-373可抑制直肠癌中TAM的M2极化,miR-373可能通过调控JAK2/STAT6通路抑制直肠癌细胞的增殖和转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[miR-373 inhibits M2 polarization of tumor associated macrophages and affects rectal cancer cells by regulating JAK2/STAT6 signal pathway].

Objective To explore the effects of miR-373 and Janus kinase 2/signal transducer and activator of transcription 6 (JAK2/STAT6) signaling pathways on the M2 polarization of tumor associated macrophages (TAM) in rectal cancer. Methods THP-1 cells were induced into M0/M1/M2 macrophages, M0 macrophages were cocultured with Caco-2 cells to obtain TAM, Flow cytometry was used to detect the expression of CD86 and CD206, Real-time quantitative qPCR and Western blot were used to detect miR-373, inducible nitric oxide synthase (iNOS), toll-like receptor 4 (TLR-4), interleukin 1β (IL-1β), tumor necrosis factor α (TNF-α), arginase 1 (Arg1), chitinase 3-like 1 (Ym1), resistin like α (Fizz1), IL-10 mRNA and protein levels. TAM were transfected and divided into overexpressing miR-373 group (miR-373-TAM) and control group (miR-NC-TAM), overexpressing miR-373+JAK2-TAM group (miR-373 combined with JAK2-TAM) and control group (miR-373 combined with NC-TAM), and then cocultured with Caco-2 cells. Flow cytometry was used to detect the expression of CD206 in TAM; Real-time quantitative PCR and Western blot were used to detect miR-373, Arg1, Ym1, Fizz1, IL-10, JAK2, STAT6 mRNA and protein levels in TAM; CCK-8 assay, colony formation assay, and Transwell assay were used to detect the proliferation, migration, and invasion ability of Caco-2 cells. Thirty nude mice were randomly divided into Caco-2 cells group, Caco-2 cells combined with miR-NC-TAM group, and Caco-2 cells combined with miR-373-TAM group, with 10 mice in each group. Rats in each group were subcutaneously injected with pure Caco-2 cells, Caco-2 cells combined with TAM, and Caco-2 cells combined with TAM overexpressing miR-373. After 4 weeks of cell inoculation, immunofluorescence staining was used to detect F4/80+CD206+cells level in tumor tissue; Real-time quantitative PCR and Western blot were used to detect miR-373, JAK2, STAT6, Arg1, Ym1, Fizz1, IL-10 mRNA and protein levels in tumor tissues. Results TAM tended to M2 polarization. After overexpression of miR-373, miR-373 level in TAM was increased, while Arg1, Ym1, Fizz1, IL-10, JAK2, STAT6 mRNA and protein levels were decreased, proliferation, migration, invasion ability of Caco-2 cells were decreased; Overexpression of JAK2 could partially reverse the effect of overexpression of miR-373 on the M2 polarization of TAM and proliferation, migration, invasion ability of Caco-2 cells. TAM could promote tumor growth; Overexpression of miR-373 could inhibit tumor growth and inhibit M2 polarization of TAM. Conclusion miR-373 could inhibit M2 polarization of TAM in rectal cancer, and miR-373 might inhibit proliferation and metastasis of rectal cancer cells by regulating the JAK2/STAT6 pathway.

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