Evidence map›Paper›PMID 26828486›Full record

ArticleInternational journal of molecular sciences2016

Mitotic Diversity in Homeostatic Human Interfollicular Epidermis.

Katharina Nöske, Hans-Jürgen Stark, Leonard Nevaril, Manuel Berning, Lutz Langbein, Ashish Goyal, Sven Diederichs, Petra Boukamp

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. CRISPR-Cas9‒Based Genomic Engineering in Keratinocytes: From Technology to Application.JID innovations : skin science from molecules to population health · 2022
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Stem Cell Activation in Adult Organisms.International journal of molecular sciences · 2016
    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

8 authors at 4 institutions in 1 country.

Katharina NöskeDepartment of Genetics of Skin Carcinogenesis, German Cancer Research Center (DKFZ), Heidelberg 69120, Germany. katharinanoeske@gmx.de.
Hans-Jürgen StarkDepartment of Genetics of Skin Carcinogenesis, German Cancer Research Center (DKFZ), Heidelberg 69120, Germany. hj.stark@dkfz.de.
Leonard NevarilDepartment of Genetics of Skin Carcinogenesis, German Cancer Research Center (DKFZ), Heidelberg 69120, Germany. L.Nevaril@dkfz.de.
Manuel BerningDepartment of Genetics of Skin Carcinogenesis, German Cancer Research Center (DKFZ), Heidelberg 69120, Germany. manuel.berning@googlemail.com.
Lutz LangbeinDepartment of Genetics of Skin Carcinogenesis, German Cancer Research Center (DKFZ), Heidelberg 69120, Germany. L.Langbein@dkfz.de.
Ashish GoyalDepartment of RNA Biology and Cancer, German Cancer Research Center (DKFZ), Heidelberg 69120, Germany. A.Goyal@dkfz.de.
Sven DiederichsDepartment of RNA Biology and Cancer, German Cancer Research Center (DKFZ), Heidelberg 69120, Germany. S.Diederichs@dkfz.de.
Petra BoukampDepartment of Genetics of Skin Carcinogenesis, German Cancer Research Center (DKFZ), Heidelberg 69120, Germany. p.boukamp@dkfz.de.
German Cancer Research Center · DEHeidelberg University · DELeibniz Institute of Environmental Medicine · DEUniversity Hospital Heidelberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite decades of skin research, regulation of proliferation and homeostasis in human epidermis is still insufficiently understood. To address the role of mitoses in tissue regulation, we utilized human long-term skin equivalents and systematically assessed mitoses during early epidermal development and long-term epidermal regeneration. We now demonstrate four different orientations: (1) horizontal, i.e., parallel to the basement membrane (BM) and suggestive of symmetric divisions; (2) oblique with an angle of 45°-70°; or (3) perpendicular, suggestive of asymmetric division. In addition, we demonstrate a fourth substantial fraction of suprabasal mitoses, many of which are committed to differentiation (Keratin K10-positive). As verified also for normal human skin, this spatial mitotic organization is part of the regulatory program of human epidermal tissue homeostasis. As a potential marker for asymmetric division, we investigated for Numb and found that it was evenly spread in almost all undifferentiated keratinocytes, but indeed asymmetrically distributed in some mitoses and particularly frequent under differentiation-repressing low-calcium conditions. Numb deletion (stable knockdown by CRISPR/Cas9), however, did not affect proliferation, neither in a three-day follow up study by life cell imaging nor during a 14-day culture period, suggesting that Numb is not essential for the general control of keratinocyte division.

Indexed as

Epidermal CellsHomeostasisMitosisAsymmetric Cell DivisionCalciumCell DifferentiationCells, CulturedEpidermisFibroblastsHEK293 CellsHumansKeratinocytesMembrane ProteinsNerve Tissue ProteinsCalciumMembrane ProteinsNerve Tissue ProteinsNUMB protein, humanasymmetric mitosisepidermal differentiationhuman epidermislong-term organotypic culture modelNumbsuprabasal mitosis

Identifiers

PMID26828486
PMCPMC4783901
OpenAlexW2284616468

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.