Dataset Information

Transcriptional Programming of Normal and Inflamed Human Epidermis at Single-Cell Resolution.

ABSTRACT: Perturbations in the transcriptional programs specifying epidermal differentiation cause diverse skin pathologies ranging from impaired barrier function to inflammatory skin disease. However, the global scope and organization of this complex cellular program remain undefined. Here we report single-cell RNA sequencing profiles of 92,889 human epidermal cells from 9 normal and 3 inflamed skin samples. Transcriptomics-derived keratinocyte subpopulations reflect classic epidermal strata but also sharply compartmentalize epithelial functions such as cell-cell communication, inflammation, and WNT pathway modulation. In keratinocytes, ?12% of assessed transcript expression varies in coordinate patterns, revealing undescribed gene expression programs governing epidermal homeostasis. We also identify molecular fingerprints of inflammatory skin states, including S100 activation in the interfollicular epidermis of normal scalp, enrichment of a CD1C+CD301A+ myeloid dendritic cell population in psoriatic epidermis, and IL1?hiCCL3hiCD14+ monocyte-derived macrophages enriched in foreskin. This compendium of RNA profiles provides a critical step toward elucidating epidermal diseases of development, differentiation, and inflammation.

SUBMITTER: Cheng JB

PROVIDER: S-EPMC6367716 | biostudies-literature | 2018 Oct

REPOSITORIES: biostudies-literature

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Publications

Transcriptional Programming of Normal and Inflamed Human Epidermis at Single-Cell Resolution.

Cheng Jeffrey B JB Sedgewick Andrew J AJ Finnegan Alex I AI Harirchian Paymann P Lee Jerry J Kwon Sunjong S Fassett Marlys S MS Golovato Justin J Gray Matthew M Ghadially Ruby R Liao Wilson W Perez White Bethany E BE Mauro Theodora M TM Mully Thaddeus T Kim Esther A EA Sbitany Hani H Neuhaus Isaac M IM Grekin Roy C RC Yu Siegrid S SS Gray Joe W JW Purdom Elizabeth E Paus Ralf R Vaske Charles J CJ Benz Stephen C SC Song Jun S JS Cho Raymond J RJ

Cell reports 20181001 4

Perturbations in the transcriptional programs specifying epidermal differentiation cause diverse skin pathologies ranging from impaired barrier function to inflammatory skin disease. However, the global scope and organization of this complex cellular program remain undefined. Here we report single-cell RNA sequencing profiles of 92,889 human epidermal cells from 9 normal and 3 inflamed skin samples. Transcriptomics-derived keratinocyte subpopulations reflect classic epidermal strata but also sha ...[more]

PMID: 30355494

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Project description:Key Points • A heme rheostat regulates normal erythropoiesis as well as the ineffective erythropoiesis of DBA and MDS-5q.• Marrow cells from patients with MDS-5q with or without the deletion of 5q share transcription profiles. Visual Abstract Abstract The anemias of myelodysplastic syndrome (MDS) and Diamond Blackfan anemia (DBA) are generally macrocytic and always reflect ineffective erythropoiesis yet result from diverse genetic mutations. To delineate shared mechanisms that lead to cell death, we studied the fate of single erythroid marrow cells from individuals with DBA or MDS-5q. We defined an unhealthy (vs healthy) differentiation trajectory using transcriptional pseudotime and cell surface proteins. The pseudotime trajectories diverge immediately after cells upregulate transferrin receptor (CD71), import iron, and initiate heme synthesis, although cell death occurs much later. Cells destined to die express high levels of heme-responsive genes, including ribosomal protein and globin genes, whereas surviving cells downregulate heme synthesis and upregulate DNA damage response, hypoxia, and HIF1 pathways. Surprisingly, 24% ± 12% of cells from control subjects follow the unhealthy trajectory, implying that heme might serve as a rheostat directing cells to live or die. When heme synthesis was inhibited with succinylacetone, more DBA cells followed the healthy trajectory and survived. We also noted high numbers of messages with retained introns that increased as erythroid cells matured, confirmed the rapid cycling of colony forming unit–erythroid, and demonstrated that cell cycle timing is an invariant property of differentiation stage. Including unspliced RNA in pseudotime determinations allowed us to reliably align independent data sets and accurately query stage-specific transcriptomic changes. MDS-5q (unlike DBA) results from somatic mutation, so many normal (unmutated) erythroid cells persist. By independently tracking erythroid differentiation of cells with and without chromosome 5q deletions, we gained insight into why 5q+ cells cannot expand to prevent anemia.

Dataset Information

Transcriptional Programming of Normal and Inflamed Human Epidermis at Single-Cell Resolution.

Publications

Transcriptional Programming of Normal and Inflamed Human Epidermis at Single-Cell Resolution.

Similar Datasets

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