Savickiene Jurate, Treigyte Grazina, Baronaite Sandra, Valiuliene Giedre, Kaupinis Algirdas, Valius Mindaugas, Arlauskiene Audrone, Navakauskiene Ruta
Department of Molecular Cell Biology, Vilnius University, LT-08662 Vilnius, Lithuania.
Proteomic Center, Institute of Biochemistry, Vilnius University, LT-08662 Vilnius, Lithuania.
Stem Cells Int. 2015;2015:319238. doi: 10.1155/2015/319238. Epub 2015 Aug 17.
Human amniotic fluid stem cells have become an attractive stem cell source for potential applications in regenerative medicine and tissue engineering. The aim of this study was to characterize amniotic fluid-derived mesenchymal stem cells (AF-MSCs) from second- and third-trimester of gestation. Using two-stage protocol, MSCs were successfully cultured and exhibited typical stem cell morphological, specific cell surface, and pluripotency markers characteristics. AF-MSCs differentiated into adipocytes, osteocytes, chondrocytes, myocytes, and neuronal cells, as determined by morphological changes, cell staining, and RT-qPCR showing the tissue-specific gene presence for differentiated cell lineages. Using SYNAPT G2 High Definition Mass Spectrometry technique approach, we performed for the first time the comparative proteomic analysis between undifferentiated AF-MSCs from late trimester of gestation and differentiated into myogenic, adipogenic, osteogenic, and neurogenic lineages. The analysis of the functional and expression patterns of 250 high abundance proteins selected from more than 1400 demonstrated the similar proteome of cultured and differentiated AF-MSCs but the unique changes in their expression profile during cell differentiation that may help the identification of key markers in differentiated cells. Our results provide evidence that human amniotic fluid of second- and third-trimester contains stem cells with multilineage potential and may be attractive source for clinical applications.
人羊水干细胞已成为再生医学和组织工程潜在应用中一种有吸引力的干细胞来源。本研究的目的是对妊娠中期和晚期的羊水来源间充质干细胞(AF-MSCs)进行表征。采用两阶段方案,成功培养出MSCs,其表现出典型的干细胞形态、特异性细胞表面和多能性标志物特征。通过形态学变化、细胞染色和RT-qPCR检测分化细胞谱系中组织特异性基因的存在情况,确定AF-MSCs可分化为脂肪细胞、骨细胞、软骨细胞、肌细胞和神经细胞。我们首次使用SYNAPT G2高分辨质谱技术方法,对妊娠晚期未分化的AF-MSCs与分化为成肌、成脂、成骨和神经谱系的细胞进行了比较蛋白质组学分析。对从1400多种蛋白质中筛选出的250种高丰度蛋白质的功能和表达模式分析表明,培养的和分化的AF-MSCs蛋白质组相似,但细胞分化过程中其表达谱有独特变化,这可能有助于识别分化细胞中的关键标志物。我们的结果提供了证据,表明妊娠中期和晚期的人羊水含有具有多向分化潜能的干细胞,可能是临床应用的有吸引力来源。