An optimised tissue disaggregation and data processing pipeline for characterising fibroblast phenotypes using single-cell RNA sequencing.
Sara WaiseRachel ParkerMatthew J J Rose-ZerilliDavid M LayfieldOliver WoodJonathan J WestChristian Hermann OttensmeierGareth J ThomasChristopher J HanleyPublished in: Scientific reports (2019)
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.
Keyphrases
- single cell
- gene expression
- rna seq
- high throughput
- dna methylation
- bone marrow
- electronic health record
- induced apoptosis
- signaling pathway
- climate change
- big data
- extracellular matrix
- cell cycle arrest
- stem cells
- minimally invasive
- cell proliferation
- risk assessment
- machine learning
- endoplasmic reticulum stress
- quality improvement
- wound healing
- human health
- data analysis