Evidence map›Paper›PMID 25358790›Full record

ArticleStem cell reports2014

BLIMP1 is required for postnatal epidermal homeostasis but does not define a sebaceous gland progenitor under steady-state conditions.

Kai Kretzschmar, Denny L Cottle, Giacomo Donati, Ming-Feng Chiang, Sven R Quist, Harald P Gollnick, Ken Natsuga, Kuo-I Lin, Fiona M Watt

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
7.0field-weighted citation impact, top 3% of its field
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

32 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Single-cell analysis of 2,3,7,8-tetrachlorodibenzo-bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Ontogeny of Skin Stem Cells and Molecular Underpinnings.Current issues in molecular biology · 2024
    Review
  5. Myc-dependent dedifferentiation of Gata6Nature cell biology · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Aging in the sebaceous gland.Frontiers in cell and developmental biology · 2022
    Review
  10. Review
  11. Article
  12. Article
  13. Development and Maintenance of Epidermal Stem Cells in Skin Adnexa.International journal of molecular sciences · 2020
    Review
  14. Article
  15. Equal opportunities in stemness.Nature cell biology · 2019
    Review
  16. TheBiology open · 2019
    Article
  17. Blimp1Nature communications · 2019
    Article
  18. Sex bias in autoimmunity.Current opinion in rheumatology · 2019
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 6 institutions in 5 countries.

Kai KretzschmarCentre for Stem Cells and Regenerative Medicine, King's College London, Guy's Hospital, 28(th) Floor Tower Wing, Great Maze Pond, London SE1 9RT, UK; Wellcome Trust-Medical Research Council Stem Cell Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, UK; Department of Genetics, University of Cambridge, Downing Street, Cambridge CB2 3EH, UK.
Denny L CottleWellcome Trust-Medical Research Council Stem Cell Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, UK; Department of Biochemistry and Molecular Biology, Monash University, Building 76, Wellington Road, Clayton, VIC 3800, Australia.
Giacomo DonatiCentre for Stem Cells and Regenerative Medicine, King's College London, Guy's Hospital, 28(th) Floor Tower Wing, Great Maze Pond, London SE1 9RT, UK; Epithelial Cell Biology Laboratory, Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK.
Ming-Feng ChiangGraduate Institute of Life Sciences, National Defense Medical Centre, Taipei 114, Taiwan, ROC; Genomics Research Center, Academia Sinica, Taipei 115, Taiwan, ROC.
Sven R QuistEpithelial Cell Biology Laboratory, Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK; Clinic of Dermatology and Venereology, Otto-von-Guericke University, Magdeburg, Leipziger Strasse 44, 39120 Magdeburg, Germany.
Harald P GollnickClinic of Dermatology and Venereology, Otto-von-Guericke University, Magdeburg, Leipziger Strasse 44, 39120 Magdeburg, Germany.
Ken NatsugaEpithelial Cell Biology Laboratory, Cancer Research UK Cambridge Research Institute, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK; Department of Dermatology, Hokkaido University Graduate School of Medicine, North 15 West 7, Sapporo 060-8638, Japan.
Kuo-I LinGraduate Institute of Life Sciences, National Defense Medical Centre, Taipei 114, Taiwan, ROC; Genomics Research Center, Academia Sinica, Taipei 115, Taiwan, ROC.
Fiona M WattCentre for Stem Cells and Regenerative Medicine, King's College London, Guy's Hospital, 28(th) Floor Tower Wing, Great Maze Pond, London SE1 9RT, UK. Electronic address: fiona.watt@kcl.ac.uk.
Guy's Hospital · GBGenomics Research Center, Academia Sinica · TWCancer Research UK · GBHokkaido University · JPOtto-von-Guericke University Magdeburg · DEWellcome/MRC Cambridge Stem Cell Institute · GB

Funding

Cancer Research UKMedical Research CouncilWellcome Trust 096540
6 · The paper itself

Abstract

B-lymphocyte-induced nuclear maturation protein 1 (BLIMP1) was previously reported to define a sebaceous gland (SG) progenitor population in the epidermis. However, the recent identification of multiple stem cell populations in the hair follicle junctional zone has led us to re-evaluate its function. We show, in agreement with previous studies, that BLIMP1 is expressed by postmitotic, terminally differentiated epidermal cells within the SG, interfollicular epidermis, and hair follicle. Epidermal overexpression of c-Myc results in loss of BLIMP1(+) cells, an effect modulated by androgen signaling. Epidermal-specific deletion of Blimp1 causes multiple differentiation defects in the epidermis in addition to SG enlargement. In culture, BLIMP1(+) sebocytes have no greater clonogenic potential than BLIMP1(-) sebocytes. Finally, lineage-tracing experiments reveal that, under steady-state conditions, BLIMP1-expressing cells do not divide. Thus, rather than defining a sebocyte progenitor population, BLIMP1 functions in terminally differentiated cells to maintain homeostasis in multiple epidermal compartments.

Indexed as

Epidermal CellsHomeostasisAdult Stem CellsAnimalsCell DifferentiationCell LineageCell ProliferationCells, CulturedHumansKeratinocytesMicePositive Regulatory Domain I-Binding Factor 1Sebaceous GlandsTranscription FactorsPositive Regulatory Domain I-Binding Factor 1Prdm1 protein, mouseTranscription Factors

Identifiers

PMID25358790
PMCPMC4223714
OpenAlexW2063503020

What OpenQuestion holds

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LicenceCC BY
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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.