人子宫内膜干细胞在体外不同传代培养中的标记谱

P. Kaingade, A. Nikam, Sachin Kulkarni, I. Somasundaram
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引用次数: 2

摘要

子宫内膜是一个动态的器官,在女性的整个生殖周期中经历着广泛的增殖和再生。因此,对子宫内膜成体干细胞的广泛研究正在进行中。鉴别干细胞的一个简单方法是它的标记特征。然而,这些标记是否在体外干细胞的所有条件下表现相同是不确定的?因此,本研究的主要目的是检查子宫内膜间充质干细胞(eMSCs)是否能在体外不同传代中保持其标志物特征。研究设计如下:选取平均年龄35±1.5岁、体重指数24±1.4、行D&C/子宫切除术的育龄妇女子宫内膜组织(n=10)。样品以无菌方式采集。从子宫内膜组织(eMSCs)分离的细胞培养中获得的可塑,粘附的间充质干细胞被表征为研究设计,通过使用流式细胞术表征eMSCs在不同传代(P1, P3, P5和P10)的一些标记物,如CD44, CD166, CD106, CD49d, CD31, CD54, CD34, CD117, CD90, CD105, CD73, CD140b, ABCG2完成。所得结果采用学生t检验进行统计分析,并对显著性结果进行讨论。本研究确定了eMSCs的组织特异性标记物,其中大多数标记物在P3和P10的表达百分比一致,除了CD49d和CD54在P10表现出减少模式,ABCG2在P10表现出与P3相比的百分比增加。本文揭示了人子宫内膜干细胞体外深度标志物表征的意义。
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Marker profiles of human endometrial stem cells at various passages cultured in-vitro
Endometrium is a dynamic organ, which undergoes extensive proliferation and regeneration throughout reproductive cycle of women. Hence, extensive research on adult stem cells of endometrium is underway. An easy approach to identify stem cells is its marker characterization. However, does these markers behave same in all conditions of stem cells in-vitro is uncertain? Hence, the main objective of the study is to check if mesenchymal stem cells of the endometrium (eMSCs) could retain its marker characterization at various passages in-vitro.   The study design was accomplished as follows: The endometrial tissue (n=10) were collected from reproductively active women with a mean age of 35±1.5 and body mass index of 24±1.4, undergoing D&C/hysterectomy. Samples were collected in a sterile manner. The plastic, adherent mesenchymal stem cells obtained from culturing of the cells isolated from endometrial tissue (eMSCs) are characterized for study design was accomplished by characterizing some of the markers such as CD44, CD166, CD106, CD49d, CD31, CD54, CD34, CD117, CD90, CD105, CD73, CD140b, ABCG2 of eMSCs at various passages (P1, P3, P5 & P10) in-vitro using flowcytometry. The obtained results were analysed statistically using student’s t-test and significant results are discussed. The study identified tissue-specific markers of eMSCs, where the percentage expression of most of the markers was consistently similar at P3 and P10, expect for CD49d and CD54, which showed a reduction pattern and ABCG2, which showed an increase in percentage at P10 as compared to P3. This article reveals the significance of in-depth marker characterization of human endometrial stem cells in-vitro.
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