当前位置:主页 > 医学论文 > 妇产科论文 >

PRL-3对子宫内膜异位症患者内膜细胞迁移能力的影响及雌、孕激素对其调控的相关性研究

发布时间:2018-06-18 17:44

  本文选题:子宫内膜异位症 + 迁移能力 ; 参考:《中南大学》2014年硕士论文


【摘要】:目的 本课题通过原代培养正常人及子宫内膜异位症患者子宫内膜细胞,比较不同细胞的形态学结构及迁移能力的差别。通过给予不同细胞雌、孕激素及原矾酸钠(SoV)干预,测定肝再生磷酸酶3(phosphatase of regenerating liver-3, PRL-3)的表达情况及变化,探讨PRL-3与子宫内膜细胞迁徙能力差异的关系,研究子宫内膜异位症高转移高侵袭的发病机制。 方法 1.原代培养正常人及子宫内膜异位症患者子宫内膜细胞,比较不同细胞的形态学结构。 2.用划线实验比较不同细胞的迁移能力差别。 3. qT-PCR法及Western Blot法测定不同细胞中PRL-3的表达。 4.予以PRL-3抑制剂原矾酸钠、雌、孕激素干预后,行划线实验确定细胞迁移能力变化。qT-PCR法及Western Blot法测定不同细胞中PRL-3的表达。 结果 1.子宫内膜细胞由腺上皮细胞及间质细胞组成,腺上皮细胞角蛋白免疫组化染色呈阳性反应,间质细胞波形蛋白免疫组化染色呈阳性反应。随着传代次数增加,角蛋白阳性细胞数量越来越少,波形蛋白阳性细胞所占比例占绝大部分,为主要细胞。 2.划线实验结果显示:在位内膜细胞在36小时后细胞迁移的距离大于正常子宫内膜细胞迁移的距离;对照组内膜细胞迁移的距离大于加入0.5umol/l SoV组细胞迁移的距离;10-6mol/l雌二醇组细胞迁移的距离大于对照组细胞迁移的距离。对照组内膜细胞迁移的距离大于10-5mol/l孕酮细胞迁移的距离。 3.PRL-3在EMs患者在位内膜上皮细胞中表达强于正常人细胞中的表达,两者之间差异有统计学意义(P0.05);对照组细胞中PRL-3表达强于加入SoV组细胞中表达,两者之间差异有统计学意义(P0.05);加入雌激素组细胞中PRL-3表达强于对照组细胞中表达,两者之间差异有统计学意义(P0.05);对照组细胞中PRL-3表达强于加入孕激素组细胞中的表达,两者之间差异有统计学意义(P0.05) 结论 1.EMs患者在位子宫内膜细胞迁移能力强于正常人子宫内膜细胞迁移能力,PRL-3在EMs在位子宫内膜细胞中表达强于正常人子宫内膜细胞,子宫内膜细胞可能通过PRL-3促进子宫内膜细胞的迁移能力。 2.雌激素可能通过上调PRL-3表达,正性调节子宫内膜细胞的迁移。孕激素可能通过下调PRL-3表达,负性调节子宫内膜细胞的迁移。 3.SoV能通过抑制PRL-3的表达,抑制子宫内膜细胞的迁移能力。
[Abstract]:Purpose

In order to study the relationship between PRL - 3 and migration ability of endometrial cells , the relationship between PRL - 3 and migration ability of endometrial cells was determined by the intervention of estrogen , progesterone and sodium sulfate ( SoV ) in different cells .

method

1 . The endometrial cells of normal and endometriosis were cultured in primary culture , and the morphological structure of different cells was compared .

2 . The difference of migration ability of different cells was compared by scoring experiment .

3 . The expression of PRL - 3 in different cells was determined by qT - PCR and Western Blot .

4 . The expression of PRL - 3 in different cells was determined by the method of qT - PCR and Western Blot .

Results

1 . The endometrial cells were composed of glandular epithelial cells and stroma cells . The cytokeratins of the glandular epithelial cells showed a positive reaction with immunohistochemical staining . The number of keratin - positive cells decreased with the increase of the number of passages , and the percentage of the positive cells of the protein - positive cells accounted for most of the cells , which were the main cells .

2 . The results showed that the migration distance of the cells after 36 hours was greater than that of normal endometrial cells .
The migration of endometrial cells in the control group was greater than that in the group of 0.5mol / l SoV group .
The distance of migration of cells from 10 - 6 mol / l estradiol group was greater than that of control group .

3 . The expression of PRL - 3 in the epithelial cells of endometriosis was significantly higher than that in normal human cells ( P0.05 ) .
The expression of PRL - 3 in the control group was stronger than that in control group ( P0.05 ) .
PRL - 3 expression in estrogen group was stronger than that in control group ( P0.05 ) .
The expression of PRL - 3 in the control group was stronger than that in control group ( P0.05 ) .

Conclusion

1 . In endometriosis , the migration ability of endometrium cells was stronger than that of normal controls , PRL - 3 expression was stronger than normal endometrium cells in endometriosis , and the migration ability of endometrial cells could be promoted by PRL - 3 .

2 . Estrogen may regulate the migration of endometrial cells by up - regulating the expression of PRL - 3 , and progesterone may regulate the migration of endometrial cells by downregulating PRL - 3 expression .

3 . SoV can inhibit the migration of endometrial cells by inhibiting the expression of PRL - 3 .
【学位授予单位】:中南大学
【学位级别】:硕士
【学位授予年份】:2014
【分类号】:R711.71

【参考文献】

相关期刊论文 前2条

1 张平;张志培;李香敏;雷杰;苏凯;李小飞;王小平;;PRL-3和RhoC在A549细胞中的表达及意义[J];中国肺癌杂志;2010年12期

2 张建龙;张萦斐;张育超;毛凯;陈双;;PRL-3调节PI3K信号通路在促进结肠癌细胞增殖侵袭中的作用[J];中山大学学报(医学科学版);2013年01期



本文编号:2036346

资料下载
论文发表

本文链接:https://www.wllwen.com/yixuelunwen/fuchankeerkelunwen/2036346.html


Copyright(c)文论论文网All Rights Reserved | 网站地图 |

版权申明:资料由用户d9e29***提供,本站仅收录摘要或目录,作者需要删除请E-mail邮箱bigeng88@qq.com