Tissue Engineering and Banking Laboratory, National Centre for Cell Science, NCCS complex, Ganeshkhind, Pune, 411007, Maharashtra, India.
Cytotechnology. 2006 May;51(1):1-5. doi: 10.1007/s10616-006-9001-z. Epub 2006 Aug 5.
The aim of our study is to explore the possibility of using an ancient method of culture technique- the hanging drop technique for stem cell differentiation and cytotoxicity testing. We demonstrate here a variety of novel applications of this age old technique not only to harness the differentiation potential of stem cells into specific lineages but also for cytotoxicity studies. Here we have prepared hanging drop cultures by placing 20 microl micro-drops of nutrient media and 10% Fetal Calf Serum (FCS) containing cells of interest on the lids of 60 mm dishes. Bottom plates of the dishes were filled with sterile Phosphate Buffer Saline (PBS) to avoid desiccation of samples. Lids were then placed on the bottom plates to achieve hanging drop cultures. We utilized this technique for cultivation of ciliated epithelia to study cytotoxicity and differentiation of bone marrow stromal cells. Most importantly the modified culture technique presented here is simple, economical and cost effective in terms of the time taken and the reagents required and are amenable to goal specific modification such as cytotoxicity testing. It is advantageous over the existing system in terms of retention of viability and functionality for longer duration and for providing three dimensional growth micro-environment making it useful for organotypic cultures and in vivo simulation.
我们研究的目的是探索一种古老的培养技术——悬滴培养技术在干细胞分化和细胞毒性检测中的应用可能性。在这里,我们展示了这种古老技术的多种新颖应用,不仅可以利用干细胞的分化潜能来诱导其向特定谱系分化,还可以用于细胞毒性研究。我们通过在 60mm 培养皿的盖子上放置 20μl 的微滴营养培养基和含有感兴趣细胞的 10%胎牛血清(FCS)来制备悬滴培养物。培养皿的底部分别填充无菌磷酸盐缓冲盐水(PBS)以避免样本干燥。然后将盖子放在底部分别上,以实现悬滴培养。我们利用该技术培养纤毛上皮细胞,以研究骨髓基质细胞的细胞毒性和分化。最重要的是,这里提出的改良培养技术简单、经济,从所需时间和试剂方面来看,成本效益高,并且易于进行特定目标的修改,如细胞毒性检测。与现有的系统相比,该技术具有更长的存活率和功能保留时间,以及提供三维生长微环境的优势,使其适用于器官培养和体内模拟。