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比较超离心和聚合物沉淀技术分离的骨髓和牙髓来源间充质干细胞外泌体的形态、蛋白浓度和大小分布。

Comparison of morphology, protein concentration, and size distribution of bone marrow and Wharton's jelly-derived mesenchymal stem cells exosomes isolated by ultracentrifugation and polymer-based precipitation techniques.

机构信息

Department of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran.

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.

出版信息

Tissue Cell. 2024 Jun;88:102427. doi: 10.1016/j.tice.2024.102427. Epub 2024 May 31.

Abstract

Exosomes which are tiny extracellular vesicles (30-150 nm), transport vital proteins and gene materials such as miRNA, mRNA, or DNA, whose role in cell communication and epithelia regulation is critical. Many techniques have been developed as a result of studying exosomes' biochemical and physicochemical properties, although there is still no standard method to isolate exosomes simply with high yield. Commercial kits have gained popularity for exosome extraction despite concerns about their effectiveness in scientific research. On the other hand, ultracentrifugation remains the gold standard isolation method. This study compares these two common exosome isolation methods to determine their impact on the quality and quantity of exosomes isolated from bone marrow (BM) and Wharton's jelly (WJ)-derived mesenchymal stem cells. Isolated exosomes from the two sources of the cell's conditioned medium by two methods (polymer kit and ultracentrifuge) were characterized using western blotting, scanning electron microscopy (SEM), dynamic light scattering (DLS), and the Bradford assay. Western blot analysis confirmed separation efficiency based on CD81 and CD63 markers, with the absence of calnexin serving as a negative control. The Morphology of exosomes studied by SEM image analysis revealed a similar round shape appearance and their sizes (30-150 nm) were the same in both isolation techniques. The DLS analysis of the sample results was consistent with the SEM ones, showing a similar size range and very low disparity. The exosome protein content concentration analysis revealed that exosomes isolated by the polymer-based kits contained higher protein concentration density and purity (p <0.001). In general, though the protein yield was higher when the polymer-based kits were used, there were no significant differences in morphology, or size between WJ-derived and BM-derived exosomes, regardless of the isolation method employed.

摘要

外泌体是微小的细胞外囊泡(30-150nm),可转运重要的蛋白质和基因物质,如 miRNA、mRNA 或 DNA,其在细胞通讯和上皮调节中的作用至关重要。许多技术已经被开发出来,以研究外泌体的生化和物理化学特性,尽管目前仍然没有一种简单且高产量的方法来分离外泌体。尽管商业试剂盒在科学研究中的有效性存在争议,但它们在提取外泌体方面已经变得很受欢迎。另一方面,超速离心仍然是分离外泌体的金标准方法。本研究比较了这两种常见的外泌体分离方法,以确定它们对骨髓(BM)和 Wharton 胶(WJ)衍生间充质干细胞来源的细胞条件培养基中分离的外泌体的质量和数量的影响。使用 Western blot、扫描电子显微镜(SEM)、动态光散射(DLS)和 Bradford 测定法,通过两种方法(聚合物试剂盒和超速离心)从两种细胞来源的细胞条件培养基中分离外泌体。Western blot 分析基于 CD81 和 CD63 标志物证实了分离效率,而 calnexin 的缺失作为阴性对照。SEM 图像分析研究的外泌体形态显示出相似的圆形外观,并且两种分离技术的大小(30-150nm)相同。样品结果的 DLS 分析与 SEM 结果一致,显示出相似的尺寸范围和非常低的差异。外泌体蛋白含量浓度分析表明,聚合物试剂盒分离的外泌体含有更高的蛋白浓度密度和纯度(p <0.001)。总的来说,尽管聚合物试剂盒法获得的蛋白产量更高,但无论采用哪种分离方法,WJ 衍生和 BM 衍生的外泌体在形态或大小上均无显著差异。

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