[1]乔艳华,赵冰*,李林玉,等.WNK 1基因对宫骶韧带成纤维细胞生长的影响[J].中国计划生育和妇产科,2020,(4):89-91,96.
 QIAO Yan hua,ZHAO Bing,*,et al.Effect of WNK 1 gene on growth of fibroblasts in the sacral ligament[J].Chinese Journal of Family Planning & Gynecotokology,2020,(4):89-91,96.
点击复制

WNK 1基因对宫骶韧带成纤维细胞生长的影响
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4期
页码:
89-91,96
栏目:
论著与临床
出版日期:
2020-04-25

文章信息/Info

Title:
Effect of WNK 1 gene on growth of fibroblasts in the sacral ligament
作者:
乔艳华1赵冰1*李林玉2王莹莹1王肖帆1张志磊1孙青1
1450001河南郑州,郑州大学第三附属医院妇产科;2 453003河南新乡,新乡医学院三全学院科教部
Author(s):
QIAO Yanhua1 ZHAO Bing1 2* LI Linyu3 WANG Yingying1 WANG Xiaofan1 ZHANG Zhilei1 SUN Qing1
1.Department of Obstetrics and Gynecology,the Third Affiliated Hospital of Zhengzhou University, Zhengzhou Henan 450001; 2. Ministry of Science and Education,Sanquan College of Xinxiang Medical College, Xinxiang Henan 453003,P.R.China
关键词:
WNK1基因宫骶韧带成纤维细胞I型胶原蛋白Ⅲ型胶原蛋白
Keywords:
WNK 1 gene uterine sacral ligamentfibroblastscollagen Ⅰcollagen Ⅲ
分类号:
R 7112
摘要:
目的 研究WNK 1基因对宫骶韧带成纤维细胞的影响。方法 采用组织块法培养大鼠宫骶韧带成纤维细胞。根据慢病毒转染的方法分为WNK 1+组、WNK 1-组和空白对照组。RTqPCR检测细胞的转染效率;CCK8法检测细胞增殖的情况;用RTqPCR和Western blot检测成纤维细胞WNK 1基因、Ⅰ型胶原蛋白、Ⅲ型胶原蛋白表达。结果 WNK 1+组的成纤维细胞的WNK 1基因表达明显高于WNK 1-组及空白对照组(P<005);镜检及CCK8检测成纤维细胞增殖数目和体积均显著增加(P<005);Westernblot及 RTqPCR结果显示WNK 1+组WNK 1激酶、Ⅰ型和Ⅲ型胶原蛋白的mRNA相对表达量及蛋白水平较WNK 1-组及空白对照组均显著增加(P<005)。结论 WNK 1基因能够促进宫骶韧带中成纤维细胞的增殖,使胶原蛋白表达增加,继而能增加宫骶韧带的弹力及张力,为患有盆底功能障碍疾病患者的诊断和治疗提供新思路。
Abstract:
ObjectiveTo study the effect of WNK 1 gene on fibroblasts of uterine sacral ligament.MethodsTissue block method was used to culture rat uterine sacral ligament fibroblasts. They were divided into WNK 1+ group, WNK 1-group and blank control group according to the method of lentivirus transfection. RTqPCR was used to detect cell transfection efficiency; CCK8 method was used to detect cell proliferation; RTqPCR and Western blot were used to detect the expression of WNK 1 gene, type Ⅰ collagen, and type Ⅲ collagen in fibroblasts. ResultsThe WNK 1 gene expression of fibroblasts in WNK 1+ group was significantly higher than that in WNK 1-group and blank control group (P<005); the number and volume of fibroblast proliferation were significantly increased under microscopic examination and CCK8 detection (P<005). Westernblot and RTqPCR results showed that the relative expression levels and protein levels of WNK 1 kinase, type Ⅰ and type Ⅲ collagen in WNK 1+ group were significantly higher than those in WNK 1-group and blank control group (P<005). ConclusionWNK 1 gene can promote the proliferation of fibroblasts in the uterine sacral ligament, increase collagen expression, and then increase the elasticity and tension of the uterine sacral ligament, providing new ideas for diagnosis and treatment of patients with pelvic floor dysfunction.

参考文献/References:

[1]Zhang Lifang, Ping Zheng, Duan Aihong, et al.Genomewide DNA methylation analysis of uterosacral ligaments in women with pelvic organ prolapse [J].Molecular Medicine Reports, 2019, 19(1): 391399. [2]Ow L L, Lim Y N, Lee J, et al.RCT of vaginal extraperitoneal uterosacral ligament suspension (VEULS) with anterior mesh versus sacrocolpopexy: 4year outcome [J].International Urogynecology Journal, 2018, 29(11): 16071614. [3]丁文娟,洪莉,吴德斌,等.机械力对子宫旁韧带成纤维细胞凋亡的作用 [J].中华妇产科杂志,2014,49(9):690693. [4]Rodan A R, Jenny A.WNK kinases in development and disease[J].Current Topics in Developmental Biology, 2017, 123(3): 147. [5]Serysheva E, Berhane H, Grumolato L, et al.Wnk kinases are positive regulatoys of canonical Wnt/catenin signaling [J].EMBO Reports, 2013, 14(8): 718725. [6]张翀,陈楠.WNK激酶的研究进展 [J].细胞生物学杂志,2008,30(6):711715. [7]Rao Shuquan, Lang Jinghe, Zhu Lan, et al.Exome sequencing identifies a novel gene, WNK1, for susceptibility to pelvic organ prolapse (POP) [J].PLOS One, 2015, 10(3): e 0119482. [8]李晓伟,苗娅莉,王建六,等.子宫骶韧带成纤维细胞受力后胶原合成变化的初步研究 [J].中华妇产科杂志,2011,46(3):172176. [9]Zhang Yajuan, Zheng Huaqing, Chen Baoyi, et al.WNK1 is required for proliferation induced by hypotonic challenge in rat vascular smooth muscle cells[J].Acta Pharmacologica Sinica, 2018, 39(1): 3547. [10]王莹莹,王君敏,陈璐璐,等.Wnt/βcatenin信号通路及WNK 1基因在盆腔脏器脱垂发病机制中的作用 [J].中国计划生育和妇产科,2019,11(5):5661. [11]龚霞.压力性尿失禁患者宫骶韧带中MMPs/TIMPs表达量、细胞外基质成分含量与细胞凋亡的关系 [J].海南医学院学报,2017,23(15):21132115, 2119. [12]Swarup S,Pradhan S T,Verheyen E M.Genomewide identification of phosphoregulators of Wnt signaling in Drosophila [J].Development (Cambridge, England),2015,142(8):15021515.

备注/Memo

备注/Memo:
河南省高校科技创新人才支持计划(项目编号:18HASTIT045)
更新日期/Last Update: 2020-04-25