Li X, Wu P L, Zhu J W, Xue Q, Yang H X
Department of Obstetrics and Gynecology, Peking University First Hospital, Beijing 100034, China.
Zhonghua Fu Chan Ke Za Zhi. 2021 Oct 25;56(10):705-711. doi: 10.3760/cma.j.cn112141-20210610-00315.
To investigate the effect and mechanism of tumor necrosis factor α (TNF-α) and its inhibitor etanercept (ETA) on the invasion ability of extravillous trophoblast in patients with unexplained recurrent spontaneous abortion (URSA). (1) Patients were collected from March to June in 2019. They were divided into the URSA group (=15) and the normal control group (=15), according to whether diagnosed with URSA or not. The mRNA expression levels of TNF-α in villi tissue of patients in the two groups were detected by quantitative real-time PCR (qRT-PCR). (2) The mRNA and protein expression levels of matrix metalloproteinase-2 (MMP-2), Slug and CXC chemokine rceptor 4 (CXCR4) in HTR-8/SVneo cells were detected by qRT-PCR or western blot after being stimulated by exogenous TNF-α (0.2, 2, 20 ng/ml) alone or TNF-α along with ETA, or phosphate buffered saline (PBS) as control. (3) The invasion ability of HTR-8/SVneo cells was investigated by transwell test after stimulating by TNF-α alone or TNF-α along with ETA. (4) The mRNA and protein expression levels of MMP-2, Slug and CXCR4 in HTR-8/SVneo cells, which were stimulated by TNF-α (2 ng/ml) alone after nuclear factor-κB (NF-κB) inhibitor, BAY 11-7028, preconditioning, were detected by qRT-PCR or western blot. (1) The mRNA expression level of TNF-α in villi tissue of URSA group (4.10±0.49) was 4.1 times as much as the normal control group (=10.51, <0.05). (2) The mRNA and protein expression levels of MMP-2, Slug and CXCR4 in HTR-8/SVneo cells of TNF-α group were significantly lower than those in PBS control group (<0.05) and those in TNF-α along with ETA group (<0.05). (3) The invasion ability of HTR-8/SVneo cells in TNF-α group was significantly decreased than PBS group and TNF-α along with ETA group (78±14 vs 373±26 vs 227±44, <0.05). (4) The mRNA and protein expression levels of MMP-2, Slug and CXCR4 in HTR-8/SVneo cells with BAY 11-7028 preconditioning (mRNA: 1.03±0.10, 1.03±0.06, 1.09±0.08; protein: 1.09±0.03, 1.49±0.03, 1.12±0.03) were significantly higher than without preconditioning after being stimulated by TNF-α (all <0.05). The expression of TNF-α in the villi of URSA patients is much higher than normal early pregnant women. TNF-α could decrease the capacity of invasion by suppressing the expression of MMP-2, Slug and CXCR4 through NF-κB signaling pathway in extravillous trophoblast cells. While ETA could improve the invasiveness capability of extravillous trophoblast cells through inhibiting the negative effect of TNF-α.
探讨肿瘤坏死因子α(TNF-α)及其抑制剂依那西普(ETA)对不明原因复发性自然流产(URSA)患者绒毛外滋养细胞侵袭能力的影响及机制。(1)收集2019年3月至6月的患者。根据是否诊断为URSA,将其分为URSA组(n = 15)和正常对照组(n = 15)。采用定量实时荧光定量PCR(qRT-PCR)检测两组患者绒毛组织中TNF-α的mRNA表达水平。(2)用外源性TNF-α(0.2、2、20 ng/ml)单独或TNF-α联合ETA刺激HTR-8/SVneo细胞后,通过qRT-PCR或蛋白质印迹法检测基质金属蛋白酶-2(MMP-2)、Slug和CXC趋化因子受体4(CXCR4)的mRNA和蛋白表达水平,以磷酸盐缓冲液(PBS)作为对照。(3)用TNF-α单独或TNF-α联合ETA刺激后,通过Transwell实验研究HTR-8/SVneo细胞的侵袭能力。(4)用核因子-κB(NF-κB)抑制剂BAY 11-7028预处理后,用TNF-α(2 ng/ml)刺激HTR-8/SVneo细胞,通过qRT-PCR或蛋白质印迹法检测MMP-2、Slug和CXCR4的mRNA和蛋白表达水平。(1)URSA组绒毛组织中TNF-α的mRNA表达水平(4.10±0.49)是正常对照组(n = 10.51,P < 0.05)的4.1倍。(2)TNF-α组HTR-8/SVneo细胞中MMP-2、Slug和CXCR4的mRNA和蛋白表达水平显著低于PBS对照组(P < 0.05)和TNF-α联合ETA组(P < 0.05)。(3)TNF-α组HTR-8/SVneo细胞的侵袭能力显著低于PBS组和TNF-α联合ETA组(78±14 vs 373±26 vs 227±44,P < 0.05)。(4)经BAY 11-7028预处理的HTR-8/SVneo细胞在TNF-α刺激后,MMP-2、Slug和CXCR4的mRNA和蛋白表达水平(mRNA:1.03±0.10、1.03±0.06、1.09±0.08;蛋白:1.09±0.03、1.49±0.03、1.12±0.03)显著高于未预处理组(均P < 0.05)。URSA患者绒毛中TNF-α的表达明显高于正常早孕妇女。TNF-α可通过抑制NF-κB信号通路降低绒毛外滋养细胞中MMP-2、Slug和CXCR4的表达,从而降低其侵袭能力。而ETA可通过抑制TNF-α的负面影响来提高绒毛外滋养细胞的侵袭能力。