Department of Pharmacy, Ningbo Municipal Hospital of Traditional Chinese Medicine, Affiliated Hospital of Zhejiang Chinese Medical University, Ningbo 315010, Zhejiang Province, China.
School of Basic Medicine, Zhejiang Chinese Medical University, Hangzhou 311499, China.
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2023 Feb 25;52(1):88-100. doi: 10.3724/zdxbyxb-2022-0353.
To investigate the mechanism of Xuanhusuo powder (XHSP) inhibiting the differentiation of spleen myeloid-derived suppressor cells (MDSCs) in breast cancer mice.
Forty-eight BALB/c female mice aged 4-5 weeks were selected, 6 of them were in normal control group, while others were in tumor-bearing models established by orthotopic injection of 4T1 cells into the subcutaneous fat pad of the second pair of left mammary glands. The tumor-bearing mice were divided into granulocyte colony stimulating factor (G-CSF) control group, G-CSF knock-down group, model control group, XHSP small dose group, XHSP medium dose group, XHSP high dose group, and cyclophosphamide (CTX) group, with 6 mice in each group. G-CSF control group and G-CSF knock-down group were constructed by stably transfecting 4T1 cells established by shRNA lentivirus combined with puromycin selection. 48 h after the model was established, XHSP small, medium, high dose group were given 2, 4, 8 g·kg·d intragastric administration once a day, respectively. CTX was given 30 mg/kg by intraperitoneal injection, once every other day. The other groups were given an equal volume of 0.5% hydroxymethylcellulose sodium. The drugs in each group were continuously administered for 25 d. Histological changes in spleen were observed by HE staining, the proportion of MDSCs subsets in the spleen were detected by flow cytometry, the co-expression of CD11b and Ly6G in the spleen was detected by immunofluorescence, and the concentration of G-CSF in peripheral blood was detected by ELISA. The spleen of tumor-bearing mice was co-cultured with 4T1 stably transfected cell lines , treated with XHSP (30 μg/mL) for 24 h, and the co-expression of CD11b and Ly6G in the spleen was detected by immunofluorescence. 4T1 cells were treated by XHSP (10, 30, 100 μg/mL) for 12 h. The mRNA level of - was detected by realtime RT-PCR.
Compared with normal mice, the red pulp of the spleen in tumor-bearing mice was widened with megakaryocyte infiltration. The proportion of spleen polymorphonucleocyte-like MDSCs (PMN-MDSCs) was significantly increased (<0.01) and the co-expression of CD11b and Ly6G was increased, and the concentration of G-CSF in peripheral blood was significantly increased (<0.01). However, XHSP could significantly reduce the proportion of PMN-MDSCs (<0.05) and the co-expression of CD11b and Ly6G in the spleen, down-regulate the mRNA level of - in 4T1 cells (<0.01). The concentration of G-CSF in peripheral blood of tumor-bearing mice also decreased (<0.05) and tumor volume was reduced and splenomegaly was improved (all <0.05).
XHSP may play an anti-breast cancer role by down-regulating G-CSF, negatively regulating the differentiation of MDSCs, and reconstruct the spleen myeloid microenvironment.
探讨玄胡索散抑制乳腺癌小鼠骨髓源性抑制细胞(MDSCs)分化的作用机制。
选取 48 只 4-5 周龄 BALB/c 雌性小鼠,其中 6 只为正常对照组,其余小鼠均采用第 2 对左乳腺皮下脂肪垫内注射 4T1 细胞建立荷瘤模型。荷瘤小鼠分为粒细胞集落刺激因子(G-CSF)对照组、G-CSF 敲低组、模型对照组、玄胡索散小剂量组、玄胡索散中剂量组、玄胡索散高剂量组和环磷酰胺(CTX)组,每组 6 只。G-CSF 对照组和 G-CSF 敲低组通过 shRNA 慢病毒联合嘌呤霉素筛选稳定转染建立的 4T1 细胞构建。模型建立 48 h 后,玄胡索散小、中、高剂量组分别给予 2、4、8 g·kg·d 灌胃,每日 1 次。CTX 按 30 mg/kg 腹腔注射,隔日 1 次。其他各组给予等体积的 0.5%羟甲基纤维素钠。各组药物连续给药 25 d。采用 HE 染色观察脾脏组织学变化,流式细胞术检测脾脏 MDSCs 亚群比例,免疫荧光法检测脾脏 CD11b 和 Ly6G 的共表达,ELISA 法检测外周血 G-CSF 浓度。将荷瘤小鼠脾脏与 4T1 稳定转染细胞系共培养,用 XHSP(30 μg/mL)处理 24 h,免疫荧光法检测脾脏 CD11b 和 Ly6G 的共表达。XHSP(10、30、100 μg/mL)处理 4T1 细胞 12 h,采用实时 RT-PCR 检测-的 mRNA 水平。
与正常小鼠相比,荷瘤小鼠脾脏红髓增宽,伴有巨核细胞浸润。脾脏多形核样 MDSCs(PMN-MDSCs)比例明显升高(<0.01),CD11b 和 Ly6G 的共表达增加,外周血 G-CSF 浓度明显升高(<0.01)。然而,玄胡索散能明显降低 PMN-MDSCs 比例(<0.05)和脾脏中 CD11b 和 Ly6G 的共表达,下调 4T1 细胞中-的 mRNA 水平(<0.01)。荷瘤小鼠外周血 G-CSF 浓度也降低(<0.05),肿瘤体积减小,脾肿大改善(均<0.05)。
玄胡索散可能通过下调 G-CSF,负调控 MDSCs 的分化,重建脾脏髓系微环境,发挥抗乳腺癌作用。