Srinivasaraghavan Vasavi Nallur, Zafar Faria, Schüle Birgitt
Department of Pathology, Stanford University School of Medicine, Stanford, USA.
Bio Protoc. 2022 Jul 20;12(14). doi: 10.21769/BioProtoc.4476.
To optimize differentiation protocols for stem cell-based modeling applications, it is essential to assess the change in gene expression during the differentiation process. This allows controlling its differentiation efficiency into the target cell types. While RNA transcriptomics provides detail at a larger scale, timing and cost are prohibitive to include such analyses in the optimization process. In contrast, expression analysis of individual genes is cumbersome and lengthy. Here, we developed a versatile and cost-efficient SYBR Green array of 27 markers along with two housekeeping genes to quickly screen for differentiation efficiency of human induced pluripotent stem cells (iPSCs) into excitatory cortical neurons. We first identified relevant pluripotency, neuroprogenitor, and neuronal markers for the array by literature search, and designed primers with a product size of 80-120 bp length, an annealing temperature of 60°C, and minimal predicted secondary structures. We spotted combined forward and reverse primers on 96-well plates and dried them out overnight. These plates can be prepared in advance in batches and stored at room temperature until use. Next, we added the SYBR Green master mix and complementary DNA (cDNA) to the plate in triplicates, ran quantitative PCR (qPCR) on a Quantstudio 6 Flex, and analyzed results with QuantStudio software. We compared the expression of genes for pluripotency, neuroprogenitor cells, cortical neurons, and synaptic markers in a 96-well format at four different time points during the cortical differentiation. We found a sharp reduction of pluripotency genes within the first three days of pre-differentiation and a steady increase of neuronal markers and synaptic markers over time. In summary, we built a gene expression array that is customizable, fast, medium-throughput, and cost-efficient, ideally suited for optimization of differentiation protocols for stem cell-based modeling.
为了优化基于干细胞建模应用的分化方案,在分化过程中评估基因表达的变化至关重要。这有助于控制其向目标细胞类型的分化效率。虽然RNA转录组学能在更大规模上提供详细信息,但在优化过程中进行此类分析的时间和成本过高。相比之下,单个基因的表达分析既繁琐又耗时。在此,我们开发了一种通用且经济高效的SYBR Green基因阵列,包含27个标记以及两个管家基因,用于快速筛选人类诱导多能干细胞(iPSC)向兴奋性皮质神经元的分化效率。我们首先通过文献检索确定了该阵列相关的多能性、神经祖细胞和神经元标记,并设计了产物大小为80 - 120 bp、退火温度为60°C且预测二级结构最小的引物。我们将正向和反向引物混合点样到96孔板上,然后 overnight 干燥。这些板可以提前批量制备并在室温下保存直至使用。接下来,我们将SYBR Green预混液和互补DNA(cDNA)一式三份加入板中,在Quantstudio 6 Flex上进行定量PCR(qPCR),并使用QuantStudio软件分析结果。我们在皮质分化的四个不同时间点,以96孔板形式比较了多能性、神经祖细胞、皮质神经元和突触标记基因的表达。我们发现预分化的前三天内多能性基因急剧减少,而神经元标记和突触标记随时间稳步增加。总之,我们构建了一种可定制、快速、中等通量且经济高效的基因表达阵列,非常适合优化基于干细胞建模的分化方案。