Biomicrofluidics. 2012 Jun;6(2):24122-2412210. doi: 10.1063/1.4719979. Epub 2012 May 22.
Embryonic stem (ES) cells are capable of proliferating and differentiating to form cells of the three embryonic germ layers, namely, endoderm, mesoderm, and ectoderm. The utilization of human ES cell derivatives requires the ability to direct differentiation to specific lineages in defined, efficient, and scalable systems. Better markers are needed to identify early differentiation. Lectins have been reported as an attractive alternative to the common stem cell markers. They have been used to identify, characterize, and isolate various cell subpopulations on the basis of the presentation of specific carbohydrate groups on the cell surface. This article demonstrates how simple adhesion assays in lectin-coated microfluidic channels can provide key information on the interaction of lectins with ES and definitive endoderm cells and thereby track early differentiation. The microfluidic approach incorporates both binding strength and cell surface receptor density, whereas traditional flow cytometry only incorporates the latter. Both approaches are examined and shown to be complementary with the microfluidic approach providing more biologically relevant information.
胚胎干细胞(ES 细胞)具有增殖和分化为三个胚胎生殖层的能力,即内胚层、中胚层和外胚层。人类 ES 细胞衍生物的利用需要能够在明确、高效和可扩展的系统中定向分化为特定谱系。需要更好的标记物来识别早期分化。凝集素已被报道为常见干细胞标记物的一种有吸引力的替代品。它们已被用于根据细胞表面上特定糖基团的呈现来识别、表征和分离各种细胞亚群。本文展示了如何在凝集素包被的微流控通道中的简单粘附测定法为凝集素与 ES 和确定的内胚层细胞的相互作用提供关键信息,从而跟踪早期分化。微流控方法结合了结合强度和细胞表面受体密度,而传统的流式细胞术仅包含后者。这两种方法都进行了检查,并显示出互补性,微流控方法提供了更具生物学相关性的信息。