Evidence map›Paper›PMID 9786957›Full record

ArticleThe Journal of cell biology1998

Functional differences between keratins of stratified and simple epithelia.

E Hutton, R D Paladini, Q C Yu, M Yen, P A Coulombe, E Fuchs

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in The Journal of cell biology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

31 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Esophageal Cancer: Insights From Mouse Models.Cancer growth and metastasis · 2015
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Context-dependent differentiation of multipotential keratin 14-expressing tracheal basal cells.American journal of respiratory cell and molecular biology · 2011
    Article
  14. Tracheal Basal cells: a facultative progenitor cell pool.The American journal of pathology · 2010
    Article
  15. Multi-scale mechanics from molecules to morphogenesis.The international journal of biochemistry & cell biology · 2009
    Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review
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

6 authors at 3 institutions in 1 country.

E HuttonHoward Hughes Medical Institute, Department of Molecular Genetics and Cell Biology, The University of Chicago, Chicago, IL 60637, USA.
R D Paladini
Q C Yu
M Yen
P A Coulombe
E Fuchs
Howard Hughes Medical Institute · USUniversity of Chicago · USJohns Hopkins University · US

Funding

GENE EXPRESSION AND DIFFERENTIATION IN HUMAN EPIDERMISR37AR027883 · NIAMS · UNIVERSITY OF CHICAGO · PI ELAINE FUCHS · 1994 to 2026
$13.3M
Non-Canonical Functions of Keratin Proteins in SkinR01AR044232 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COULOMBE, PIERRE · 1996 to 2020
$8.6M
GENE EXPRESSION &DIFFERENTIATION IN HUMAN EPIDERMISR01AR027883 · NIAMS · UNIVERSITY OF CHICAGO · PI FUCHS, ELAINE · 1986 to 2022
$7.6M
NIAMS NIH HHS AR27883NIAMS NIH HHS AR44232NIAMS NIH HHS R01 AR027883NIAMS NIH HHS R01 AR044232NIAMS NIH HHS R37 AR027883
6 · The paper itself

Abstract

Dividing populations of stratified and simple epithelial tissues express keratins 5 and 14, and keratins 8 and 18, respectively. It has been suggested that these keratins form a mechanical framework important to cellular integrity, since their absence gives rise to a blistering skin disorder in neonatal epidermis, and hemorrhaging within the embryonic liver. An unresolved fundamental issue is whether different keratins perform unique functions in epithelia. We now address this question using transgenic technology to express a K16-14 hybrid epidermal keratin transgene and a K18 simple epithelial keratin transgene in the epidermis of mice null for K14. Under conditions where the hybrid epidermal keratin restored a wild-type phenotype to newborn epidermis, K18 partially but not fully rescued. The explanation does not appear to reside in an inability of K18 to form 10-nm filaments with K5, which it does in vitro and in vivo. Rather, it appears that the keratin network formed between K5 and K18 is deficient in withstanding mechanical stress, leading to perturbations in the keratin network in regions of the skin that are subjected either to natural or to mechanically induced trauma. Taken together, these findings suggest that the loss of a type I epidermal keratin cannot be fully compensated by its counterpart of simple epithelial cells, and that in vivo, all keratins are not equivalent.

Indexed as

Epidermal CellsAnimalsBlisterDermatologic AgentsEpidermisEpithelial CellsGene ExpressionHumansIntermediate FilamentsKeratin-14KeratinsMiceMice, TransgenicMicroscopy, ElectronProtein BindingStress, MechanicalDermatologic AgentsKeratin-14KeratinsKRT14 protein, humanKrt14 protein, mouseUrea

Identifiers

PMID9786957
PMCPMC2132837
OpenAlexW2073852580

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.