Xiao Biru, Xue Xiangyang, Hu Feihong, Sun Rongrong, Chen Qiuyue, Yang Mengmeng, Zhang Wenmiao
Department of Obstetrics and Gynecology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, China.
Email:
Zhonghua Fu Chan Ke Za Zhi. 2014 Feb;49(2):130-4.
To study the expression and the mechanism of miR-155in the villi of patients with unexplained recurrent spontaneous abortion (URSA).
The expression of miR-155 in the villi of 36 cases with URSA (URSA group) and 25 women with normal early pregnancy (control group) were detected by stem-loop real-time reverse transcription (RT) qPCR.Expression of hypoxia inducible factor-1 (HIF-1α), vascular endothelial cell growth factor (VEGF) and micro lymphatic vessel density (MVD) in the villi of were measured by immnohistochemical staining among two groups.
(1)miR-155 expression:the mean miR-155 expression were 1.456 (0.489, 2.459) in URSA group and 2.833 (1.740, 3.794) in control group, which reached statistical difference (P < 0.05). The mean expression of miR-155 of 1.683 (0.902, 2.459) in URSA group with abortion times ( ≤ 3) was significantly higher than 1.229 (0.489, 1.719) in URSA group with more than 4 times abortion (P < 0.05). (2) Indexes :the expression of HIF-1α, VEGF and MVD value were 121 ± 12, 134 ± 12, 36 ± 6 in URSA group and 99 ± 10, 109 ± 10, 28 ± 4 in control group, which reached statistical difference (P < 0.01). The expression of HIF-1α, VEGF and MVD value of 119 ± 12, 134 ± 12, 35 ± 5 in URSA group with less than 3 times abortion was significantly lower than 128 ± 12, 138 ± 12, 43 ± 6 in URSA group with more than 4 times abortion (P < 0.01).
The expression of miR-155 and HIF-1α is topically stimulated by oxygen signal.HIF-1α adjusts the transcription and translation of VEGF, which together involved in placental trophoblast invasion and placental angiogenesis. The low expression of miR-155 could interfere with expression of HIF-1α and VEGF, which might be involved in villous vascular dysplasia in URSA.
研究miR-155在不明原因复发性自然流产(URSA)患者绒毛中的表达及机制。
采用茎环实时逆转录(RT)qPCR检测36例URSA患者(URSA组)和25例正常早孕妇女(对照组)绒毛中miR-155的表达。通过免疫组织化学染色检测两组绒毛中缺氧诱导因子-1(HIF-1α)、血管内皮细胞生长因子(VEGF)的表达及微淋巴管密度(MVD)。
(1)miR-155表达:URSA组miR-155平均表达量为1.456(0.489,2.459),对照组为2.833(1.740,3.794),差异有统计学意义(P<0.05)。流产次数≤3次的URSA组miR-155平均表达量为1.683(0.902,2.459),显著高于流产次数>4次的URSA组的1.229(0.489,1.719)(P<0.05)。(2)指标:URSA组HIF-1α、VEGF表达量及MVD值分别为121±12、134±12、36±6,对照组为99±10、109±10、28±4,差异有统计学意义(P<0.01)。流产次数<3次的URSA组HIF-1α、VEGF表达量及MVD值分别为119±12、134±12、35±5,显著低于流产次数>4次的URSA组的128±12、138±12、43±6(P<0.01)。
miR-155和HIF-1α的表达受氧信号局部刺激。HIF-1α调节VEGF的转录和翻译,共同参与胎盘滋养细胞侵袭和胎盘血管生成。miR-155低表达可能干扰HIF-1α和VEGF的表达,这可能与URSA患者绒毛血管发育异常有关。