
浏览全部资源
扫码关注微信
1. 重庆医科大学公共卫生与管理学院生殖生物研究室
2. 重庆医科大学附属第一医院妇产科
纸质出版日期:2017,
扫 描 看 全 文
[1]杨洋,吴梦云,李荣,王应雄,刘学庆.Mmu-miR-24对小鼠着床期子宫内膜基质细胞和蜕膜细胞的调节作用[J].重庆医科大学学报,2017,42(08):959-964.
Yang Yang, Wu Mengyun, Li Rong, et al. Effect of Mmu-miR-24 on endometrial stromal and decidual cells during early pregnancy in mice[J]. Journal of Chongqing Medical University, 2017,42(8):959-964.
[1]杨洋,吴梦云,李荣,王应雄,刘学庆.Mmu-miR-24对小鼠着床期子宫内膜基质细胞和蜕膜细胞的调节作用[J].重庆医科大学学报,2017,42(08):959-964. DOI: 10.13406/j.cnki.cyxb.001337.
Yang Yang, Wu Mengyun, Li Rong, et al. Effect of Mmu-miR-24 on endometrial stromal and decidual cells during early pregnancy in mice[J]. Journal of Chongqing Medical University, 2017,42(8):959-964. DOI: 10.13406/j.cnki.cyxb.001337.
目的:探讨mmu-mi R-24在小鼠子宫内膜基质细胞和蜕膜细胞中的作用。方法:收集妊娠第1、4、5、6天(D1、D4、D5、D6)的小鼠子宫;分离小鼠基质细胞
体外激素人工诱导蜕膜化。实时定量PCR(real-time quantitative PCR
q RT-PCR)、原位杂交(in situ hybridization
ISH)以及蛋白印迹(Western blot)检测mmu-mi R-24及相应因子的表达。采用脂质体2000转染mmumi R-24模拟物(mimics)及抑制物(inhibitor)模型上调或下调mmu-mi R-24表达后
检测细胞凋亡与细胞周期。结果:mmumi R-24在D1高表达
且表达量高于D4(P=0.003)。mmu-mi R-24在D4的腔上皮、腺上皮及少量基质细胞中表达
而在妊娠第5天着床点(D5implantation site
D5IS)及妊娠第6天着床点(D6IS)的蜕膜区表达
且D5IS的表达量高于第5天着床旁(D5interimplantation site
D5IIS)的表达量
但无统计差异(P=0.094)。在基质细胞中
mimics干扰后
S期的细胞数降低(P=0.000)
增殖因子PCNA表达降低
总凋亡细胞数目增加(P=0.042)
凋亡因子BAX表达增高;通过inhibitor干扰后
G1期细胞数降低(P=0.005)
S期与G2期细胞数有所升高(P=0.075
P=0.054)
PCNA表达增多
晚期凋亡细胞数目减少(P=0.009)
BAX表达降低。在蜕膜细胞中
mimics干扰后
与对照组相比
G1期细胞数升高(P=0.002)
S期细胞数降低(P=0.000)
PCNA表达降低
晚期凋亡细胞数目增加(P=0.025)
BAX表达增多;inhibitor干扰后
与对照组相比
S期细胞数升高(P=0.026)
PCNA表达增多;晚期凋亡细胞数目减少(P=0.006)
BAX表达降低。结论:在胚胎植入前
mmu-mi R-24的低表达可促进基质细胞的增殖;在胚胎植入期
mmu-mi R-24的高表达可促进蜕膜细胞凋亡
有利于妊娠的维持。
Objective:To explore the effect of micro RNA-24(mmu-miR-24)in endometrial stromal cells during early pregnancy in mice. Methods:Uterus tissues were collected on pregnancy of day 1
4
5
6(D1
D4
D5
D6). The expressions of mmu-miR-24 and other factors were detected by real-time quantitative PCR(q RT-PCR)
in situ hybridization
and Western blot. The primary stromal cells were induced by estradiol(E2)and progesterone(P4)for decidulization. Flow cytometry was implemented to detect cell cycle and cell apoptosis. Results:The expression of mmu-miR-24 was detected in uterine luminal
glandular epithelium
and stromal cell on Day 4. The expression level of mmu-miR-24 on D5 IS was higher than the level on D5 IIS. On D5 IS and D6 IS
mmu-miR-24 was located in decidual zone. When mmu-miR-24 mimics being incorporated into stromal cells
the number of stromal cells in the S phase was decreased
the expression of PCNA was decreased
the total apoptotic cell was increased
and the expression of BAX was increased. In contrast
when mmu-miR-24 inhibitor being incorporated into stromal cells
the number of stromal cells in G1 phase and S phase were decreased and increased respectively
and PCNA expression level was increased
the number of non-viable apoptotic cell was decreased
and BAX level was decreased in stormal cells. On the other hand
when incorporating mmu-miR-24 mimics into the decidual cells
the number of decidual cells in the S phase was decreased
and PCNA expression level was decreased
the number of non-viable apoptotic cell was increased
and BAX level was increased in decidual cells. Lastly
when treating decidual cells with mmu-miR-24 inhibitor
the number of decidual cells in the S phase was increased
and PCNA expression level was increased
the number of non-viable apoptotic cell was decreased
and BAX level was decreased in decidual cells. Conclusion:The low expression of mmu-miR-24 in stromal cells may promote the progress of cell proliferation. The high expression of mmu-miR-24 in decidual cells may promote the progress of cell apoptosis during decidulization.
mmu-miR-24胚胎植入蜕膜化细胞凋亡细胞增殖
mmu-miR-24embryo implantationdecidulizationcell proliferationcell apoptosis
0
浏览量
130
下载量
1
CSCD
关联资源
相关文章
相关作者
相关机构
京公网安备11010802024621