首页|慢病毒载体介导的类固醇生成因子-1沉默调控子宫内膜基质细胞蜕膜化与自噬

慢病毒载体介导的类固醇生成因子-1沉默调控子宫内膜基质细胞蜕膜化与自噬

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目的 探讨慢病毒载体介导的类固醇生成因子-1(SF-1)沉默对人子宫内膜基质细胞(hESCs)蜕膜化进程的影响及机制。方法 收集子宫内膜异位症(EM)患者与正常妊娠者的子宫内膜组织,通过Real-time PCR和免疫组织化学染色检测SF-1的差异表达情况。从正常妊娠者的子宫内膜组织中分离并鉴定hESCs,将hESCs分为对照组、雌二醇(E2)+孕酮(P4)组、短发夹RNA(shRNA,sh)-正常对照(NC)+E2+P4 组、sh-SF-1+E2+P4 组,进行对应处理后,倒置显微镜下观察hESCs形态变化,Real-time PCR和Western blotting分别检测细胞内人胰岛素样生长因子结合蛋白 1(IGFBP-1)、泌乳素(PRL)的mRNA表达水平和蛋白表达水平,流式细胞术测定细胞周期分布,免疫荧光染色观察细胞内自噬标记物微管相关蛋白轻链 3(LC3)表达情况,Western blotting测定细胞内自噬相关蛋白LC3-Ⅱ、LC3-Ⅰ、Beclin-1表达水平。结果 EM患者子宫内膜组织中SF-1 mRNA相对表达量和SF-1蛋白阳性率均高于正常妊娠者子宫内膜组织(P<0。05)。与sh-NC+E2+P4 组比较,sh-SF-1+E2+P4 组细胞多为长梭形,未见明显蜕膜化,IGFBP1、PRL的 mRNA相对表达量与蛋白相对表达量均显著下调(P<0。05),G0/G1 期细胞比例显著减少而S期细胞比例显著增加(P<0。05),细胞内LC3 荧光表达增强,LC3-Ⅱ/LC3-Ⅰ比值显著升高,Beclin-1 蛋白相对表达量也显著上调(P<0。05)。结论 EM 患者子宫内膜组织内SF-1 表达升高,通过慢病毒载体介导的SF-1 沉默能够抑制hESCs蜕膜化过程,该作用可能与调控细胞自噬水平相关。
Lentiviral vector mediated steroidogenic factor-1 silencing regulating decidualization and autophagy of endometrial stromal cells
Objective To explore the influence and mechanism of lentiviral vector-mediated steroidogenic factor-1(SF-1)silence on decidual process of human endometrial stromal cells(hESCs).Methods The endometrial tissues of patients with endometriosis(EM)and normal pregnant women were collected,and the differential expression of SF-1 was detected by Real-time PCR and immunohistochemical staining.hESCs were isolated from the endometrial tissue of normal pregnancy and identified,hESCs were divided into control group,estradiol(E2)+progesterone(P4)group,short hairpin RAN(shRNA,sh)-normal control(NC)+E2+P4 group,sh-SF-1+E2+P4 group,after the corresponding processing,the morphological changes of hESCs were observed under an inverted microscope.Real-time PCR and Western blotting were used to detect the mRNA expression levels and protein levels of human insulin-like growth factor-binding protein-1(IGFBP-1)and prolactin(PRL)in cells,respectively,flow cytometry was used to determine the cycle distribution of the cells,immunofluorescence staining was used to observe the expression of the intracellular auto-bid microtubule-associated protein light chain 3(LC3),Western blotting was used to determine the protein level of intracellular autophagy-related proteins LC3-Ⅱ,LC3-Ⅰ and Beclin-1.Results The relative expression of SF-1 mRNA and the positive rate of SF-1 protein in endometrial tissue of EM patients were higher than those of normal pregnancy endometrial tissue(P<0.05).Compared with the sh-NC+E2+P4 group,the cells in the sh-SF-1+E2+P4 group were mostly long-spindle,and there was no obvious decidualization.The relative mRNA expression and protein expression of IGFBP1 and PRL were significantly down-regulated(P<0.05),the proportion of cells in G0/G1 phase was significantly decreased,the proportion of cells in S phase was significantly increased(P<0.05),the ratio of LC3-Ⅱ/LC3-Ⅰwas significantly increased,and the relative expression of Beclin-1 protein was also significantly up-regulated(P<0.05).Conclusion The expression of SF-1 in the endometrial tissue of EM patients is increased,and SF-1 silencing mediated by lentiviral vector can inhibit the decidualization process of hESCs,which may be related to regulating the level of autophagy.

Endometrial stromal cellSteroidogenic factor-1DecidualizationAutophagyWestern blottingHuman

任健、陈晓燕

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江苏大学医学院病理学教研室,江苏 镇江 212000

无锡市康复医院心肺康复科,江苏 无锡 214000

重庆市中医院妇产科,重庆 400000

子宫内膜基质细胞 类固醇生成因子-1 蜕膜化 自噬 免疫印迹法

重庆市自然科学基金

cstc2019jcyjmsxmX0749

2024

解剖学报
中国解剖学会

解剖学报

CSTPCD
影响因子:0.462
ISSN:0529-1356
年,卷(期):2024.55(2)
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