Grupo de Terapia Celular y Medicina Regenerativa. Dpto. de Fisioterapia, Medicina y Ciencias Biomédicas, Facultad de Ciencias de la Salud, Universidade da Coruña, INIBIC-CHUAC, Agrupación estratégica CICA-INIBIC, A Coruña, Spain.
Department of Food Technology, Institute of Marine Research (IIM), Spanish National Research Council (CSIC), Vigo, Spain.
Methods Mol Biol. 2021;2259:3-12. doi: 10.1007/978-1-0716-1178-4_1.
In the present protocol, extracellular vesicles (EVs) released from a primary culture of human umbilical cord mesenchymal stem cells (MSCs) were isolated by ultracentrifugation processes, characterized by transmission electron microscopy (TEM) and measured by nanoparticle tracking analysis (NTA). Protein was extracted from EVs using RIPA buffer and then was assessed for integrity. The proteomic content of the total EV protein samples was analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) after labeling by tandem mass tag (TMT). This combined approach allowed the development of an effective strategy to study the protein cargo from MSC-derived EVs.
在本方案中,通过超速离心过程从人脐带间充质干细胞(MSCs)的原代培养物中分离出外泌体(EVs),通过透射电子显微镜(TEM)进行表征,并通过纳米颗粒跟踪分析(NTA)进行测量。使用 RIPA 缓冲液从 EVs 中提取蛋白质,然后评估其完整性。通过液相色谱-串联质谱(LC-MS/MS)对总 EV 蛋白样品进行分析,并用串联质量标签(TMT)进行标记。这种联合方法为研究 MSC 来源的 EV 中的蛋白质货物开发了一种有效的策略。