Liang Zhou, Zhu Jing, Wang Yunfei, Wang You, Zhang Yu, Lin Jianhua, Di Wen
Department of Obstetrics and Gynecology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China.
Department of Obstetrics and Gynecology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China; Shanghai Key Laboratory of Gynecologic Oncology, Shanghai 200127, China. Email:
Chin Med J (Engl). 2014;127(12):2252-8.
How the transcriptional factors regulated the innate and adaptive immune system in pregnancy and pre-eclampsia are less understood. Nevertheless, what the plasma work in the development of this disease was not sure. The present study was design to evaluate what the transcriptional factors change in innate and adaptive immune system and what the plasma do in this filed.
Peripheral blood mononuclear cells (PBMC) from non-pregnant women (n = 18), women with clinically normal pregnancies (n = 23) and women with pre-eclampsia (n = 20) were separated from peripheral blood to isolate monocytes and T cells. The purity of monocytes and T cells were analysed by flow cytometry. Monocytes and T cells were stimulated in either lipopolysaccharides (LPS) or phorbol-myristate-acetate (PMA), respectively. Transcription Factor Arrays were used to screen the transcription factors of interest in comparing of different groups. PBMC were isolated from another 8 non-pregnant samples were co-incubated with different groups of plasma. Polymerase chain reaction (PCR) was performed using whole cell extractions of the samples.
Nuclear factor of activated T-cells-1 (NFAT-1), signal transducers and activators of transcription-1 (STAT-1) and activator protein-1 (AP-1) are up-regulated in monocytes in pregnancy and more so in pre-eclampsia. On the the contrary, NFAT-1, STAT-1 and AP-1 are down-regulated in T cells in pregnancy and more so in pre-eclampsia. A reduction was observed in interferon (IFN)-γ, interleukin (IL)-12 and IL-4 expression in T cells incubated with pre-eclamptic plasma. An elevation was observed in tumor necrosis factor (TNF)-α, IL-1 and IL-12 expression in monocytes incubated with pre-eclamptic plasma.
Innate immunity is over activated and adaptive immunity is over suppressed in the development of pre-eclampsia. NFAT-1, STAT-1 and AP-1 might be the central transcription factors in the pathogenesis of pre-eclampsia. They induced some changes in plasma and "educate" the monocytes and T cells for relevant cytokine production. Successful completion of this study will enhance our understanding of pre-eclampsia and will discover new knowledge beyond pregnancy. The work will inform future therapies for the treatment of a wide range of condition such as transplantation immunology and a wide range of immune and inflammatory conditions.
转录因子如何调控孕期及子痫前期的先天性和适应性免疫系统尚不清楚。然而,血浆在该疾病发展过程中的作用尚不明确。本研究旨在评估先天性和适应性免疫系统中转录因子的变化以及血浆在这方面的作用。
从非妊娠女性(n = 18)、临床妊娠正常女性(n = 23)和子痫前期女性(n = 20)的外周血中分离外周血单个核细胞(PBMC),以分离单核细胞和T细胞。通过流式细胞术分析单核细胞和T细胞的纯度。单核细胞和T细胞分别用脂多糖(LPS)或佛波酯-肉豆蔻酸酯-乙酸酯(PMA)刺激。转录因子阵列用于筛选不同组中感兴趣的转录因子。从另外8个非妊娠样本中分离的PBMC与不同组的血浆共同孵育。使用样本的全细胞提取物进行聚合酶链反应(PCR)。
活化T细胞核因子-1(NFAT-1)、信号转导子和转录激活子-1(STAT-1)以及活化蛋白-1(AP-1)在孕期单核细胞中上调,在子痫前期中上调更明显。相反,NFAT-1、STAT-1和AP-1在孕期T细胞中下调,在子痫前期中下调更明显。在用子痫前期血浆孵育的T细胞中,观察到干扰素(IFN)-γ、白细胞介素(IL)-12和IL-4表达降低。在用子痫前期血浆孵育的单核细胞中,观察到肿瘤坏死因子(TNF)-α、IL-1和IL-12表达升高。
子痫前期发展过程中先天性免疫过度激活,适应性免疫过度抑制。NFAT-1、STAT-1和AP-1可能是子痫前期发病机制中的关键转录因子。它们诱导血浆发生一些变化,并“指导”单核细胞和T细胞产生相关细胞因子。本研究的成功完成将增进我们对子痫前期的理解,并发现孕期以外的新知识。这项工作将为未来治疗多种病症提供信息,如移植免疫学以及多种免疫和炎症性疾病。