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小鼠脂肪间质干细胞源胞外囊泡激活蛋白激酶B促进卵巢癌细胞增殖迁移和上皮间质转化
引用本文:沈娜惠,孙晓春. 小鼠脂肪间质干细胞源胞外囊泡激活蛋白激酶B促进卵巢癌细胞增殖迁移和上皮间质转化[J]. 江苏大学学报(医学版), 2022, 32(1): 38-43,49. DOI: 10.13312/j.issn.1671-7783.y210062
作者姓名:沈娜惠  孙晓春
作者单位:(1. 江苏大学医学院,江苏 镇江 212013; 2. 常州市第四人民医院检验科,江苏 常州 213000)
摘    要:目的:探讨小鼠脂肪间质干细胞(adipose-derived mesenchymal stem cells,ADSCs)源胞外囊泡(extracellular vesicles,EVs)对卵巢癌ID8细胞株生物功能的影响及其可能机制。方法:采用酶消化法分离获得ADSCs,利用其形态特征、成骨成脂多向分化能力和流式细胞术表面标志检测对ADSCs进行鉴定;采用超速离心法从ADSCs上清液中分离和纯化EVs(ADSC-EVs),并通过透射电子显微镜、纳米粒径分析和蛋白质印迹实验进行鉴定;以PBS作为对照组,实验组采用不同浓度ADSC-EVs(20 μg/mL和40 μg/mL)分别预处理ID8细胞,通过平板克隆实验检测ADSC-EVs对ID8细胞增殖能力的影响;划痕实验和Transwell实验检测ADSC-EVs对ID8细胞迁移能力的影响;蛋白质印迹实验检测ID8细胞上皮间质转化(epithelial-mesenchymal transition,EMT)和蛋白激酶B(即AKT)相关蛋白的表达。结果:分离的ADSCs具有典型的干细胞形态,能够向成骨成脂分化,并符合干细胞表面一般特征;ADSC-EVs表达CD9和CD81蛋白;与PBS组相比,ADSC-EVs组ID8细胞增殖和迁移能力明显增强(P均<0.05),且40 μg/mL ADSC-EVs组细胞增殖和迁移能力较20 μg/mL ADSC-EVs组明显增强(P均<0.05);随着ADSC-EVs浓度增加,ID8细胞E-钙黏蛋白表达明显降低,N-钙黏蛋白、波形蛋白和p-AKT表达明显增加(P均<0.05)。结论:ADSC-EVs可能通过激活AKT信号的磷酸化促进ID8细胞EMT,进而增强其增殖和迁移能力。

关 键 词:卵巢癌  脂肪间质干细胞  胞外囊泡  上皮间质转化  蛋白激酶B  
收稿时间:2021-04-12

ADSC-EVs activate protein kinase B to promote the proliferation and migration and epithelial-mesenchymal transition of ovarian cancer cells
SHEN Nahui,SUN Xiaochun. ADSC-EVs activate protein kinase B to promote the proliferation and migration and epithelial-mesenchymal transition of ovarian cancer cells[J]. Journal of Jiangsu University Medicine Edition, 2022, 32(1): 38-43,49. DOI: 10.13312/j.issn.1671-7783.y210062
Authors:SHEN Nahui  SUN Xiaochun
Affiliation:(1. School of Medicine, Jiangsu University, Zhenjiang Jiangsu 212013; 2. Clinical laboratory, Changzhou Fourth People′s Hospital, Changzhou Jiangsu 213000, China)
Abstract:Objective: To explore the effect of extracellular vesicles (EVs) derived from mouse adipose-derived mesenchymal stem cells(ADSCs) on the biological behaviors of ovarian cancer ID8 cell line and its possible mechanism. Methods: ADSCs were isolated by enzyme digestion method, and identified by morphological characteristics, osteogenic and adipogenic multidirectional differentiation ability and flow cytometry surface marker detection; EVs were isolated and purified from supernatant of ADSCs by ultracentrifugation, and ADSC-EVs were identified by transmission electron microscopy, nanoparticle size analysis and Western blotting; ID8 cells were treated with ADSC-EVs at different concentrations (20 μg/mL and 40 μg/mL) and PBS as the control group. The effect of ADSC-EVs on the proliferation of ID8 cells was detected by plate cloning assay. Wound healing and Transwell test were used to detect the effect of ADSC-EVs on the migration ability of ID8 cells. The expression of epithelial-mesenchymal transition(EMT) and protein kinase B(AKT) related proteins in ID8 cells were detected by Western blotting. Results: The isolated ADSCs had typical stem cell morphology, could differentiate into osteogenesis and adipogenesis, and consistent with the general characteristics of the stem cell surface. ADSC-EVs expressed CD9 and CD81 proteins. Compared with the PBS group, the proliferation and migration of ID8 cells in ADSC-EVs group were significantly enhanced (P<0.05), and the proliferation and migration of ID8 cells in 40 μg/mL ADSC-EVS group was stronger than that in 20 μg/mL ADSC EVS group (P<0.05). With the increase of ADSC-EVS concentration, the expression of E-cadherin in ID8 cells was significantly decreased, while the expression of N-cadherin, vimentin and p Akt was greatly increased (P<0.05). Conclusion: ADSC-EVs may promote the EMT of ID8 cells by activating the phosphorylation of AKT signal, thereby enhancing their proliferation and migration ability.
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