Evidence map›Paper›PMID 16374453›Full record

ArticleThe Journal of investigative dermatology2006

Epidermal development and wound healing in matrix metalloproteinase 13-deficient mice.

Bettina Hartenstein, Bernd Thilo Dittrich, Dominique Stickens, Babette Heyer, Thiennu H Vu, Sibylle Teurich, Marina Schorpp-Kistner, Zena Werb, Peter Angel

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  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 3 institutions in 2 countries.

Bettina HartensteinDivision of Signal Transduction and Growth Control (A100), Deutsches Krebsforschungszentrum Heidelberg (DKFZ), Heidelberg, Germany.
Bernd Thilo Dittrich
Dominique Stickens
Babette Heyer
Thiennu H Vu
Sibylle Teurich
Marina Schorpp-Kistner
Zena Werb
Peter Angel
University of California, San Francisco · USHeidelberg University · DEDKFZ-ZMBH Alliance · DE

Funding

PROTEASES--TUMOR BIOLOGYP01CA072006 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WERB, ZENA · 1997 to 2007
$10.8M
Extracellular remodeling in bone development and repairR01AR046238 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WERB, ZENA · 1999 to 2010
$3.1M
NCI NIH HHS CA72006NCI NIH HHS P01 CA072006NIAMS NIH HHS AR46238NIAMS NIH HHS R01 AR046238
6 · The paper itself

Abstract

Degradation of the extracellular matrix, which is an indispensable step in tissue remodelling processes such as embryonic development and wound healing of the skin, has been attributed to collagenolytic activity of members of the matrix metalloproteinase family (MMPs). Here, we employed mmp13 knockout mice to elucidate the function of MMP13 in embryonic skin development, skin homeostasis, and cutaneous wound healing. Overall epidermal architecture and dermal composition of non-injured skin were indistinguishable from wild-type mice. Despite robust expression of MMP13 in the early phase of wound healing, wild-type and mmp13 knockout animals did not differ in their efficiency of re-epithelialization, inflammatory response, granulation tissue formation, angiogenesis, and restoration of basement membrane. Yet, among other MMPs also expressed during wound healing, MMP8 was found to be enhanced in wounds of MMP13-deficient mice. In summary, skin homeostasis and also tissue remodelling processes like embryonic skin development and cutaneous wound healing are independent of MMP13 either owing to MMP13 dispensability or owing to functional substitution by other collagenolytic proteinases such as MMP8.

Indexed as

Wound HealingAnimalsCollagenasesEpidermal CellsEpidermisGranulation TissueMatrix Metalloproteinase 13Matrix Metalloproteinase 8MiceMice, KnockoutNeovascularization, PhysiologicPhenotypeSkinCollagenasesMatrix Metalloproteinase 13Matrix Metalloproteinase 8Mmp13 protein, mouse

Identifiers

PMID16374453
PMCPMC2767339
OpenAlexW2004222333

What OpenQuestion holds

Textmetadata
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.