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沙眼衣原体感染后大鼠蜕膜中TRAIL及受体的表达 被引量:4

Expressions of TRAIL and its receptor in decidual tissues of rats after chlamydia trachomatis infection
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摘要 目的:通过大鼠生殖道沙眼衣原体(Chlamydia trachomatis,CT)感染模型研究CT初次感染后妊娠大鼠在胚胎着床期子宫蜕膜组织中肿瘤坏死因子相关凋亡诱导配体(tumor necrosis factor related apoptosis-inducing ligand,TRAIL)及其受体1(TRAIL receptor1,TRAIL R1or DR4)的mRNA及蛋白表达,探讨TRAIL/TRAILR在妊娠中的作用。方法:选择成年雌性SD大鼠38只,随机均分为实验组和对照组,实验组孕前阴道成功接种CTD型株。胚胎植入期处死大鼠,计数胚胎植入数;子宫组织分为两份,分别用来逆转录扩增(RT-PCR)半定量检测TRAIL、DR4的mRNA的相对表达量及免疫组化法确定其蛋白表达,SPSS软件处理数据分析差异显著性。结果:①实验组胚胎植入数下降(P<0.01)。②实验组DR4的mRNA高表达,差异有统计学意义(P<0.001);TRAIL的mRNA表达差异无统计学意义(P>0.05);DR4mRNA的表达量与对应的胚胎植入数呈负相关(r=-0.782,P<0.05)。③实验组TRAIL免疫组化阳性颗粒的平均光密度值差异无统计学意义(P>0.05);实验组DR4升高,差异有统计学意义(P<0.01)。结论:雌性大鼠生殖道感染CT后,胚胎植入数减少,这种变化可能与子宫组织DR4的高表达、与TRAIL过量结合导致细胞凋亡过度有关。 Objective:To research the expressions of mRNA and protein of tumor necrosis factor related apoptosis-inducing ligand (TRAIL) and its receptor 1 (TRAIL R1 or DR4) in uterine decidual tissues at implantation period of pregnant rat models with primary infection of chlamydia trachomatis,explore the functions of TRAIL/TRAILR in pregnancy.Methods:38 adult female SD rats were selected and divided into experimental group and control group randomly.The rats in experimental group were vaginally infected with D strain of chlamydia trachomatis;all the rats were sacrificed at implantation period,the number of implanted embryo was counted;the uterine tissues were divided into two subgroups to detect the relative expression levels of TRAIL and DR4 mRNA by RT-PCR and the expressions of TRAIL and DR4 protein by immunohistochemical staining,SPSS software was used in the study.Results:The number of implanted embryo in experimental group decreased significantly (P0.01).The expression level of DR4 mRNA in experimental group was high,there was significant difference (P0.001),but there was no significant difference in expression level of TRAIL mRNA between the two groups (P0.05);there was a negative correlation between expression level of DR4 mRNA and corresponding number of implanted embryo (γ=-0.782,P0.05).There was no significant difference in average optical density of immunohistochemical positive particles between the two groups (P0.05);the expression of DR4 in experimental group increased significantly (P0.01).Conclusion:The number of implanted embryo decreases after reproductive tract infection of chlamydia trachomatis in female rats,the change may be related to excessive apoptosis induced by high expression of DR4 in uterine tissues and its excessive combination with TRAIL.
出处 《中国妇幼保健》 CAS 北大核心 2010年第24期3477-3480,共4页 Maternal and Child Health Care of China
基金 湖北省人口计生委项目〔301130993〕
关键词 沙眼衣原体 胚胎植入 TRAIL DR4 Chlamydia trachomatis Embryo implantation Tumor necrosis factor related apoptosis-inducing ligand DR4
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参考文献9

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同被引文献62

  • 1李晓兰.宫颈癌发病年轻化趋势分析[J].中国妇幼保健,2007,22(23):3206-3207. 被引量:36
  • 2李晓兰,秦彩蓉,田葵珍.阴道镜和宫颈液基细胞学检查在诊断宫颈早期病变中的比较[J].中国妇产科临床杂志,2007,8(5):343-345. 被引量:20
  • 3Jemal A, Bray F, Center MM, et al. Global cancer statistics [ J]. CA CaneerJ Clin, 2011, 61 (2) : 69-90.
  • 4Gottwaht L, Szwalski J, Piekarski J, et al. Membrane expression of the death ligand trail receptors DR4 and DR5 in the normal endometri- urn, endometrial atypical hyperplasia and endometrioid endometrial cancer [J]. J Obstet Gynaecol, 2013, 33 (5): 512-518.
  • 5James MA, Seibel WL, Kupert E, et al. A novel, soluble com- pound, C25, sensitizes to TRAIL-induced apoptosis through upreg- ulation of DR5 expression [J]. Anticaneer Drugs, 2015, 26 (5) : 518-530.
  • 6Cordier SM, Papenfuss K, Walczak H, et al. From biochemical principles of apoptosis induction by TRAIL to application in tumonr Therapy [J]. Results Probl Cell Differ, 2009, 49 (14) : 115- 143.
  • 7Akram KM, Lomas N J, Forsyth NR, et al. Alveolar epithelial cells in idiopathic pulmonary fibrosis display upregulation of TRAIL, DR4 and DR5 expresskm with simultaneous preferential over-expression of pro-apoptotic marker p53 [J]. Int J Clin Exp Pathol, 2014, 7 (2) : 552-564.
  • 8Gurbuz V, Konac E, Varol N, et al. Effects of AG490 and $31 201 oll regulation of the JAK/STAT3 signaling pathway in relation to an- giogenesis in TRAIL resistant prostate cancer cells in vitro [ J]. On- col Lett, 2014, 7 (3): 755-763.
  • 9Hu JK, Yang K, l,i CM, et al. The expression of TRAIL and its receptors in gastric cancer and the apoptotic effect of rh-TRAIL on SGC7901 cells [J]. Oncol Rep, 2009, 21 (3): 681-688.
  • 10Kang YH, Park MG, Nob KH, et al. Low serum TNF-related ap- optosis-inducing ligand (TRAIL) levels are associated with acute is- chemic stroke severity [ J ]. Atherosclerosis, 2015, 240 ( 1 ) : 228-233.

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