Evidence map›Paper›PMID 29391249›Full record

ArticleThe Journal of investigative dermatology2018

Spatial and Single-Cell Transcriptional Profiling Identifies Functionally Distinct Human Dermal Fibroblast Subpopulations.

Christina Philippeos, Stephanie B Telerman, Bénédicte Oulès, Angela O Pisco, Tanya J Shaw, Raul Elgueta, Giovanna Lombardi, Ryan R Driskell, Mark Soldin, Magnus D Lynch and 1 more

Abstract read
In one paragraph

Article in The Journal of investigative dermatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 256 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
256citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

256 citing papers in PubMed, 1 synthesis or guideline pooled it.

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196 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Christina PhilippeosKing's College London Centre for Stem Cells and Regenerative Medicine, Guy's Hospital, Great Maze Pond, London, UK.
Stephanie B TelermanKing's College London Centre for Stem Cells and Regenerative Medicine, Guy's Hospital, Great Maze Pond, London, UK.
Bénédicte OulèsKing's College London Centre for Stem Cells and Regenerative Medicine, Guy's Hospital, Great Maze Pond, London, UK.
Angela O PiscoKing's College London Centre for Stem Cells and Regenerative Medicine, Guy's Hospital, Great Maze Pond, London, UK.
Tanya J ShawKing's College London Centre for Molecular and Cellular Biology of Inflammation, London, UK.
Raul ElguetaKing's College London MRC Centre for Transplantation, Guy's Hospital, Great Maze Pond, London, UK.
Giovanna LombardiKing's College London MRC Centre for Transplantation, Guy's Hospital, Great Maze Pond, London, UK.
Ryan R DriskellKing's College London Centre for Stem Cells and Regenerative Medicine, Guy's Hospital, Great Maze Pond, London, UK; School of Molecular Medicine, College of Veterinary Medicine, Washington State University, Pullman, Washington, USA.
Mark SoldinDepartment of Plastic and Reconstructive Surgery, St. George's National Health Service Trust, London, UK.
Magnus D LynchKing's College London Centre for Stem Cells and Regenerative Medicine, Guy's Hospital, Great Maze Pond, London, UK; St. John's Institute of Dermatology, Tower Wing, Guy's Hospital, Great Maze Pond, London, UK.
Fiona M WattKing's College London Centre for Stem Cells and Regenerative Medicine, Guy's Hospital, Great Maze Pond, London, UK. Electronic address: fiona.watt@kcl.ac.uk.

Funding

Medical Research Council G1100073Medical Research Council MR/K019732/2Medical Research Council MR/P018823/1Wellcome Trust
6 · The paper itself

Abstract

Previous studies have shown that mouse dermis is composed of functionally distinct fibroblast lineages. To explore the extent of fibroblast heterogeneity in human skin, we used a combination of comparative spatial transcriptional profiling of human and mouse dermis and single-cell transcriptional profiling of human dermal fibroblasts. We show that there are at least four distinct fibroblast populations in adult human skin, not all of which are spatially segregated. We define markers permitting their isolation and show that although marker expression is lost in culture, different fibroblast subpopulations retain distinct functionality in terms of Wnt signaling, responsiveness to IFN-γ, and ability to support human epidermal reconstitution when introduced into decellularized dermis. These findings suggest that ex vivo expansion or in vivo ablation of specific fibroblast subpopulations may have therapeutic applications in wound healing and diseases characterized by excessive fibrosis.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsAnimals, NewbornCells, CulturedDermisExtracellular MatrixFibroblastsFlow CytometryHumansMicePolymerase Chain ReactionRNASignal TransductionWnt ProteinsWound HealingRNAWnt Proteins

Identifiers

PMID29391249
PMCPMC5869055

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.