[1]华人意,程蔚蔚*.人羊膜细胞中趋化因子的表达及调节机制[J].中国计划生育和妇产科,2020,(6):51-54.
 HUA Renyi,CHENG Weiwei*.Expression and regulation mechanism of chemokine in human amniotic cells[J].Chinese Journal of Family Planning & Gynecotokology,2020,(6):51-54.
点击复制

人羊膜细胞中趋化因子的表达及调节机制
分享到:

《中国计划生育和妇产科》[ISSN:1674-4020/CN:51-1708/R]

卷:
期数:
2020年6期
页码:
51-54
栏目:
论著与临床
出版日期:
2020-06-25

文章信息/Info

Title:
Expression and regulation mechanism of chemokine in human amniotic cells
作者:
华人意 程蔚蔚*
上海交通大学附属国际和平妇幼保健院产前诊断中心
Author(s):
HUA RenyiCHENG Weiwei*
Prenatal Diagnosis Center,International Peace Maternity and Child Health Hospital Affiliated to Shanghai Jiaotong University,Shanghai 200030,P.R.China
关键词:
早产趋化因子羊膜细胞
Keywords:
preterm laborchemokinesamnion
分类号:
R 392.12
摘要:
目的通过体外模拟分娩时的炎症内环境,了解羊膜细胞在分娩启动中发挥的作用。方法随机选取2018年1~6月中国福利会国际和平妇幼保健院产科足月择期剖宫产病例,分为研究组和对照组,每组6例。取新鲜完整胎盘,分离羊膜细胞进行细胞培养。按分组加入白介素1β(interleukin 1 beta,IL1β)、肿瘤坏死因子α(tumor necrosis factor alpha,TNFα )、前列腺素E 2 (prostaglandin E 2,PGE 2)及前列腺素F 2α(prostaglandin F 2 alpha ,PGF 2α),于1 h、6 h和24 h收获细胞。检测羊膜细胞中各趋化因子的表达。结果在IL1β /TNFα的作用下,羊膜细胞中趋化因子CCL 2,CCL 5,CCL 20,CXCL 1,CXCL 5和CXCL 8表达增加,而在前列腺素作用下趋化因子CCL 2,CCL 5,CXCL 1,CXCL 8表达下调,CCL 20表达增加。结论本研究展现了分娩过程中羊膜细胞中的免疫调节变化,羊膜细胞通过分泌趋化因子诱导分娩炎症反应,可能早于子宫肌中的炎症反应。本研究为了解分娩启动机制提供了依据。
Abstract:
ObjectiveBy simulating the inflammatory internal environment during labor in vitro, we can understand the role of amnion cells in labor initiation. MethodsRandomly selected cases of full-term cesarean section from the Obstetrics Department of International Peace Maternity and Child Health Hospital of China Welfare Society from January to June 2018 were divided into a research group and a control group,each with 6 cases.Take fresh intact placenta, isolate amniotic membrane cells for cell culture. Add interleukin 1β (interleukin 1 beta, IL1β), tumor necrosis factor alpha (tumor necrosis factor alpha, TNFα), prostaglandin E 2 (prostaglandin E 2, PGE 2) and prostaglandin F 2α (prostaglandin F 2 alpha, PGF 2α). Cells were harvested at 1 h, 6 h and 24 h. Detect the expression of various chemokines in amniotic cells.ResultsUnder the action of IL1β / TNFα, the expression of chemokines CCL 2, CCL 5, CCL 20, CXCL 1, CXCL 5 and CXCL 8 increased in amniotic cells, while the expression of chemokines CCL 2, CCL 5, CXCL 1 and CXCL 8 under the action of prostaglandins downregulated, CCL 20 expression increased.ConclusionThis study demonstrates the changes in immune regulation in amniotic cells during labor. Amniotic cells secrete chemokines to induce inflammatory responses during labor, which may be earlier than those in uterine muscle. This study provides a basis for understanding the mechanism of labor delivery.

参考文献/References:

[1]Liu Li, Johnson H L, Cousens S, et al. Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000 [J]. Lancet, 2012, 379(9832): 21512161. [2]Mwaniki M K, Atieno M, Lawn J E, et al. Longterm neurodevelopmental outcomes after intrauterine and neonatal insults: a systematic review [J]. Lancet, 2012, 379(9814): 445452. [3]Saigal S, Doyle L W. An overview of mortality and sequelae of preterm birth from infancy to adulthood [J]. Lancet, 2008, 371(968): 261269. [4]Petrou S, Eddama O, Mangham L. A structured review of the recent literature on the economic consequences of preterm birth [J]. Archives of Disease in ChildhoodFetal and Neonatal Edition, 2011, 96(3): F 225F 232. [5]Goldenberg R L, Culhane J F, Iams J D, et al. Epidemiology and causes of preterm birth [J]. The Lancet, 2008, 371(966): 7584. [6]Osman I, Young A, Ledingham M A, et al. Leukocyte density and proinflammatory cytokine expression in human fetal membranes, decidua, cervix and myometrium before and during labour at term [J]. Molecular Human Reproduction, 2003, 9(1): 4145. [7]Hua Renyi, Jams E P, Cheng Wei, et al. Human labour is associated with a decline in myometrial chemokine receptor expression:The role of prostaglandins,oxytocin and cytokines [J]. American Journal of Reproductive Immunology, 2013, 69(1): 2132. [8]Chaurdong H, Erika M, Aversa K, et al. The role of amniotic fluid Lselectin, GROα, and interleukin8 in the pathogenesis of intraamniotic infection [J]. American Journal of Obstetrics and Gynecology, 1998, 178(3): 428432. [9]Hua R, Pease J E, Sooranna S R, et al. Stretch and inflammatory cytokines drive myometrial chemokine expression via NFkappaB activation [Z], 2011. [10]Gayle D A, Beloosesky R, Desai Mina, et al. Maternal LPS induces cytokines in the amniotic fluid and corticotropin releasing hormone in the fetal rat brain [J]. American Journal of PhysiologyRegulatory Integrative and Comparative Physiology, 2004, 286(6): R 1024R 1029. [11]Nadeauvallée M, Obari Dima, Quiniou C, et al. A critical role of interleukin1 in preterm labor [J]. Cytokine & Growth Factor Reviews, 2016, 28(3): 3751. [12]Bartlett S R, Sawdy R, Mann G E. Induction of cyclooxygenase2 expression in human myometrial smooth muscle cells by interleukin1beta:involvement of p38 mitogenactivated protein kinase [Z], 1999: 399406. [13]Hua Renyi, James E P, Sooranna S R, et al. Stretch and inflammatory cytokines drive myometrial chemokine expression via NFκB activation [J]. Endocrinology, 2012, 153(1): 481491. [14]Pourali L, Saghafi N, Eslami Hasan Abadi S, et al. Induction of labour in term premature rupture of membranes; oxytocin versus sublingual misoprostol:a randomised clinical trial [J]. Journal of Obstetrics and Gynaecology: the Journal of the Institute of Obstetrics and Gynaecology, 2018, 38(2): 167171. [15]Menon R, Fortunato S J. Fetal membrane inflammatory cytokines: a switching mechanism between the preterm premature rupture of the membranes and preterm labor pathways [J]. Journal of Perinatal Medicine, 2004, 32(5): 391399. [16]Dobreva M P, Pereira P G, Deprest J, et al. On the origin of amniotic stem cells: of mice and men [J]. The International Journal of Developmental Biology, 2010, 54(5): 761777. [17]Esplin M S , Romero R , Chaiworapongsa T , et al. Monocyte chemotactic protein1 is increased in the amniotic fluid of women who deliver preterm in the presence or absence of intraamniotic infection [J]. Journal of Maternal Fetal & Neonatal Medicine, 2005, 17(6):365373. [18]Li Haochuan, Niederkorn J Y, Neelam S, et al. Immunosuppressive factors secreted by human amniotic epithelial cells [J]. Investigative Ophthalmology & Visual Science, 2005, 46(3): 900907. [19]Laudanski P, Lemancewicz A, Kuc P, et al. Chemokines profiling of patients with preterm birth [J]. Mediators of Inflammation, 2014,2014: 185758. doi: 10.1155/2014/185758. Epub 2014 Apr 28.

相似文献/References:

[1]张泽华,陈晓勤,赵小玉,等.早产与社会环境因素[J].中国计划生育和妇产科,2010,(04):0.
 ZHANG Ze-hua,CHEN Xiao-qin,ZHAO Xiao-yu,et al.[J].Chinese Journal of Family Planning & Gynecotokology,2010,(6):0.
[2]严琴,祝茹.57例早产胎膜早破孕妇的支原体检测分析[J].中国计划生育和妇产科,2011,(02):0.
[3]顾敏贞,朱梅英,杨祖铭,等.区域内胎龄≤33周早产儿不同转运模式与预后关系的研究[J].中国计划生育和妇产科,2013,(06):0.
 Gu Min-zhen,ZHU Mei-ying,Yang Zu-ming,et al.[J].Chinese Journal of Family Planning & Gynecotokology,2013,(6):0.
[4]邹丽颖,张为远.早产诊断的变迁[J].中国计划生育和妇产科,2015,(04):0.
[5]马玉燕,朱晓丹.早产的妊娠结局[J].中国计划生育和妇产科,2015,(04):0.
[6]付晶,苟文丽.早产相关因素研究进展[J].中国计划生育和妇产科,2015,(04):0.
[7]刘小华,程蔚蔚.早产的药物治疗[J].中国计划生育和妇产科,2015,(05):0.
[8]何书励,马良坤,刘俊涛,等.早产和营养[J].中国计划生育和妇产科,2015,(05):0.
[9]虞娇,周琼洁,李笑天,等.早产预测的临床应用价值评价[J].中国计划生育和妇产科,2015,(05):0.
[10]杜楚颖,张建平.早产的预防[J].中国计划生育和妇产科,2015,(05):0.

更新日期/Last Update: 2020-06-25