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An optimised tissue disaggregation and data processing pipeline for characterising fibroblast phenotypes using single-cell RNA sequencing

机译:优化的组织分解和数据处理管道用于使用单细胞RNA测序表征成纤维细胞表型

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摘要

Single-cell RNA sequencing (scRNA-Seq) provides a valuable platform for characterising multicellular ecosystems. Fibroblasts are a heterogeneous cell type involved in many physiological and pathological processes, but remain poorly-characterised. Analysis of fibroblasts is challenging: these cells are difficult to isolate from tissues, and are therefore commonly under-represented in scRNA-seq datasets. Here, we describe an optimised approach for fibroblast isolation from human lung tissues. We demonstrate the potential for this procedure in characterising stromal cell phenotypes using scRNA-Seq, analyse the effect of tissue disaggregation on gene expression, and optimise data processing to improve clustering quality. We also assess the impact of in vitro culture conditions on stromal cell gene expression and proliferation, showing that altering these conditions can skew phenotypes.
机译:单细胞RNA测序(scRNA-Seq)为表征多细胞生态系统提供了宝贵的平台。成纤维细胞是涉及许多生理和病理过程的异质细胞类型,但特征仍然很差。成纤维细胞的分析具有挑战性:这些细胞很难从组织中分离出来,因此在scRNA-seq数据集中通常代表性不足。在这里,我们描述了从人肺组织分离成纤维细胞的优化方法。我们展示了该程序使用scRNA-Seq表征基质细胞表型的潜力,分析了组织分解对基因表达的影响,并优化了数据处理以提高聚类质量。我们还评估了体外培养条件对基质细胞基因表达和增殖的影响,表明改变这些条件可以使表型偏斜。

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