Evidence map›Paper›PMID 27066886›Full record

ArticleThe Journal of investigative dermatology2016

Fibroblast-Derived MMP-14 Regulates Collagen Homeostasis in Adult Skin.

Paola Zigrino, Jürgen Brinckmann, Anja Niehoff, Yinhui Lu, Nives Giebeler, Beate Eckes, Karl E Kadler, Cornelia Mauch

Open access · hybridAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% 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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 83 citations in OpenAlex.

  1. Pooled it
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  14. Matrix Metalloproteinases on Skin Photoaging.Journal of cosmetic dermatology · 2024
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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 2 countries.

Paola ZigrinoDepartment of Dermatology and Venerology, University of Cologne, Cologne, Germany. Electronic address: Paola.Zigrino@uni-koeln.de.
Jürgen BrinckmannDepartment of Dermatology, University of Lübeck, Lübeck, Germany; Institute of Virology and Cell Biology, University of Lübeck, Lübeck, Germany.
Anja NiehoffInstitute of Biomechanics and Orthopaedics, German Sport University and Cologne Center for Musculoskeletal Biomechanics, University of Cologne, Cologne, Germany.
Yinhui LuWellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, UK.
Nives GiebelerDepartment of Dermatology and Venerology, University of Cologne, Cologne, Germany.
Beate EckesDepartment of Dermatology and Venerology, University of Cologne, Cologne, Germany.
Karl E KadlerWellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, UK.
Cornelia MauchDepartment of Dermatology and Venerology, University of Cologne, Cologne, Germany.
University of Cologne · DEUniversity of Lübeck · DEUniversity of Manchester · GBWellcome Centre for Cell-Matrix Research · GB

Funding

Wellcome Trust 091840/Z/10/ZWellcome Trust 110126/Z/15/Z
6 · The paper itself

Abstract

Proteolytic activities in the extracellular matrix by the matrix metalloproteinase (MMP)-14 have been implicated in the remodeling of collagenous proteins during development. To analyze the function of fibroblast-derived MMP-14 in adult skin homeostasis, we generated mice with inducible deletion of MMP-14 in the dermal fibroblast (MMP-14(Sf-/-)). These mice are smaller and display a fibrosis-like phenotype in the skin. The skin of these mice showed increased stiffness and tensile strength but no altered collagen cross-links. In vivo, we measured a significantly increased amount of collagen type I accumulated in the skin of MMP-14(Sf-/-) mice without an increase in collagen fibril diameters. However, bleomycin-induced fibrosis in skin proceeded in a comparable manner in MMP-14(Sf+/+) and MMP-14(Sf-/-) mice, but resolution over time was impaired in MMP-14(Sf-/-) mice. Increased accumulation of collagen type I was detected in MMP-14(Sf-/-) fibroblasts in culture without significant enhancement of collagen de novo synthesis. This points to a degradative but not synthetic phenotype. In support of this, MMP-14(Sf-/-) fibroblasts lost their ability to process fibrillar collagen type I and to activate proMMP-2. Taken together, these data indicate that MMP-14 expression in fibroblasts plays a crucial role in collagen remodeling in adult skin and largely contributes to dermal homeostasis underlying its pathogenic role in fibrotic skin disease.

Indexed as

AnimalsBleomycinCollagenFemaleFibroblastsFibrosisGene Expression ProfilingHomeostasisInflammationMaleMatrix Metalloproteinase 14MiceMice, KnockoutPhenotypeSkinStress, MechanicalBleomycinCollagenMatrix Metalloproteinase 14Mmp14 protein, mouse

Identifiers

PMID27066886
PMCPMC4946792
OpenAlexW2316277876

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.