A Single-Cell Transcriptome Atlas of the Mouse Glomerulus.
Nikos KaraiskosMahdieh RahmatollahiAnastasiya BoltengagenHaiyue LiuMartin HöhneMarkus RinschenBernhard SchermerThomas BenzingNikolaus RajewskyChristine KocksMartin KannRoman-Ulrich MüllerPublished in: Journal of the American Society of Nephrology : JASN (2018)
Background Three different cell types constitute the glomerular filter: mesangial cells, endothelial cells, and podocytes. However, to what extent cellular heterogeneity exists within healthy glomerular cell populations remains unknown.Methods We used nanodroplet-based highly parallel transcriptional profiling to characterize the cellular content of purified wild-type mouse glomeruli.Results Unsupervised clustering of nearly 13,000 single-cell transcriptomes identified the three known glomerular cell types. We provide a comprehensive online atlas of gene expression in glomerular cells that can be queried and visualized using an interactive and freely available database. Novel marker genes for all glomerular cell types were identified and supported by immunohistochemistry images obtained from the Human Protein Atlas. Subclustering of endothelial cells revealed a subset of endothelium that expressed marker genes related to endothelial proliferation. By comparison, the podocyte population appeared more homogeneous but contained three smaller, previously unknown subpopulations.Conclusions Our study comprehensively characterized gene expression in individual glomerular cells and sets the stage for the dissection of glomerular function at the single-cell level in health and disease.
Keyphrases
- single cell
- high glucose
- endothelial cells
- rna seq
- diabetic nephropathy
- gene expression
- high throughput
- induced apoptosis
- cell cycle arrest
- healthcare
- mesenchymal stem cells
- dna methylation
- genome wide
- cell death
- machine learning
- health information
- vascular endothelial growth factor
- nitric oxide
- signaling pathway
- wild type
- oxidative stress
- cell therapy
- human health
- binding protein
- pluripotent stem cells
- optical coherence tomography