AO Research Institute, AO Foundation, Davos, Switzerland.
Biotechniques. 2019 Dec;67(6):286-293. doi: 10.2144/btn-2019-0038. Epub 2019 Oct 17.
To identify differential expression of noncoding RNAs after trypsinization in human mesenchymal stromal cells (hMSCs), focusing on miRNAs, piRNAs and circRNAs. hMSCs from the bone marrow of three donors were collected for RNA extraction, either lysed directly in monolayer or trypsinized and lysed within 30 min. Total RNA was isolated and sequenced for the evaluation of miRNA and piRNA expression or RNaseR treated and labeled for circRNA array hybridization. RT-qPCR was performed to evaluate the stability of candidate reference genes. Alterations in levels of several noncoding RNAs are rapidly induced after trypsinization of hMSCs, affecting critical pathways. This should be carefully considered for a proper experimental design.
为了鉴定人骨髓间充质干细胞(hMSCs)经胰蛋白酶消化后非编码 RNA 的差异表达,特别是 miRNA、piRNA 和 circRNA。从 3 名供者的骨髓中收集 hMSC 进行 RNA 提取,要么直接在单层中裂解,要么在 30 分钟内胰蛋白酶消化和裂解。提取总 RNA 并进行测序,以评估 miRNA 和 piRNA 的表达,或用 RNaseR 处理和标记进行 circRNA 阵列杂交。进行 RT-qPCR 以评估候选参考基因的稳定性。hMSC 经胰蛋白酶消化后,几种非编码 RNA 的水平迅速发生改变,影响关键途径。这在进行适当的实验设计时应予以仔细考虑。