γ-三烯醇修饰CD4+T淋巴细胞中HOXA10、IRF4和RORα基因的甲基化:来自癌症同基因小鼠模型的证据

Q4 Immunology and Microbiology Current research in immunology Pub Date : 2021-01-01 DOI:10.1016/j.crimmu.2021.10.001
Ammu K. Radhakrishnan , Jeya Seela Anandha Rao , Shonia Subramaniam , Premdass Ramdas
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摘要

DNA甲基化在naïve淋巴细胞向其不同亚群极化以对抗包括肿瘤建立在内的许多免疫挑战中起着至关重要的作用。γ -生育三烯醇(γT3)是维生素E的一种天然形式,据报道具有抗癌和免疫调节作用。本研究利用同基因乳腺癌小鼠模型,报道了γT3通过调节CD4+ t淋巴细胞中几个基因的DNA甲基化而具有抗癌作用。雌性BALB/c小鼠分别灌胃γ - t3或大豆油,灌胃2周后再接种4T1小鼠乳腺癌细胞。继续补充,直到小鼠被处死。尸检时,通过心脏穿刺采集血液,分离CD4+ t细胞进行DNA提取。采用EpiTech Methyl II小鼠t辅助细胞分化PCR阵列对DNA进行分析。在肿瘤诱导的动物中,补充γ - t3可通过诱导参与CD4+ t细胞分化和克隆扩增的HOXA10、IRF4和RORα基因的DNA甲基化模式改变,降低肿瘤生长,并调节宿主免疫系统。结果表明,γ - t3可能通过诱导DNA甲基化模式的改变来增强乳腺癌小鼠细胞介导的免疫应答。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Gamma-tocotrienol modifies methylation of HOXA10, IRF4 and RORα genes in CD4+ T-lymphocytes: Evidence from a syngeneic mouse model of breast cancer

DNA methylation plays a crucial role in polarising naïve lymphocytes towards their various sub-populations to fight against many immune challenges including establishment of tumour. Gamma-tocotrienol (γT3) is a natural form of vitamin E, reported to possess anticancer and immunomodulatory effects. This study reports the anticancer effects of γT3 through modulation of DNA methylation in several genes in CD4+ T-lymphocytes using a syngeneic mouse model of breast cancer. Female BALB/c mice were fed with γT3 or vehicle (soy oil) for two-weeks via oral gavage before they were inoculated with 4T1 mouse mammary cancer cells. Supplementation continued until the mice were sacrificed. At autopsy, blood was collected via cardiac puncture and CD4+ T-cells were isolated for DNA extraction. The DNA was analysed using the EpiTech Methyl II mouse T-helper cell differentiation PCR array. γT3 supplementation reduced tumour growth in the tumour-induced animals and modulated host immune system by inducing changes in DNA methylation patterns of the HOXA10, IRF4 and RORα genes, which are involved in differentiation and clonal expansion of CD4+ T-cells. Results suggest that γT3 may enhance cell-mediated immune response in mice with breast cancer by inducing changes in DNA methylation pattern.

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