Qiu P, Lin X, Deng G
Department of Gynecology, First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou 510405, China.
First Clinical Medical College of Guangzhou University of Chinese Medicine, Guangzhou 510405, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2022 Apr 20;42(4):610-617. doi: 10.12122/j.issn.1673-4254.2022.04.19.
To investigate the expression of Talin1 in the fallopian tube and chorionic villi in patients with tubal pregnancy and its role in regulating invasion and migration of trophoblasts.
Immunohistochemistry and Western blotting were used to detect the localization and expression level of Talin1 in the fallopian tube and chorionic villi in patients with tubal pregnancy and in women with normal pregnancy. In the cell experiment, HTR-8/SVneo cells was transfected with Talin1 siRNA and the changes in cell invasion and migration were assessed using scratch assay and Transwell assay. The expressions of MMP-2, MMP-9, N-cadherin and Snail in the transfected cells were detected by qRT-PCR and Western blotting.
Positive expression of Talin1 was detected in both normal fallopian tube tissues and tissues from women tubal pregnancy, and its expression was localized mainly in the cytoplasm of cilia cells. The expression level of Talin1 was significantly higher in both the fallopian tube and chorionic villi in women with tubal pregnancy than in normal fallopian tube and chorionic villi samples ( < 0.01). In HTR-8/SVneo cells, transfection with Talin1 siRNA significantly inhibited cell invasion ( < 0.01) and migration ( < 0.05), down-regulated the expression of N-cadherin, MMP-2 and Snail ( < 0.05), and up-regulated the expression of MMP-9 in the cells ( < 0.05).
The expression of Talin1 in the fallopian tube and chorionic villi is significantly increased in women with tubal pregnancy, suggesting the association of Talin1-regulated trophoblast cell invasion with the occurrence of tubal pregnancy.
探讨Talin1在输卵管妊娠患者输卵管及绒毛组织中的表达情况及其对滋养细胞侵袭和迁移的调控作用。
采用免疫组织化学和蛋白质免疫印迹法检测输卵管妊娠患者及正常妊娠女性输卵管及绒毛组织中Talin1的定位及表达水平。细胞实验中,将Talin1小干扰RNA转染至HTR-8/SVneo细胞,采用划痕实验和Transwell实验评估细胞侵袭和迁移的变化。通过实时荧光定量聚合酶链反应和蛋白质免疫印迹法检测转染细胞中基质金属蛋白酶-2(MMP-2)、基质金属蛋白酶-9(MMP-9)、N-钙黏蛋白和Snail的表达。
正常输卵管组织及输卵管妊娠患者组织中均检测到Talin1阳性表达,其表达主要定位于纤毛细胞的细胞质。输卵管妊娠患者输卵管及绒毛组织中Talin1的表达水平显著高于正常输卵管及绒毛组织样本(<0.01)。在HTR-8/SVneo细胞中,转染Talin1小干扰RNA可显著抑制细胞侵袭(<0.01)和迁移(<0.05),下调N-钙黏蛋白、MMP-2和Snail的表达(<0.05),上调细胞中MMP-9的表达(<0.05)。
输卵管妊娠患者输卵管及绒毛组织中Talin1表达显著增加,提示Talin1调控的滋养细胞侵袭与输卵管妊娠的发生有关。