Evidence map›Paper›PMID 28300207›Full record

ArticleScientific reports2017

Both Drosophila matrix metalloproteinases have released and membrane-tethered forms but have different substrates.

Kimberly S LaFever, Xiaoxi Wang, Patrick Page-McCaw, Gautam Bhave, Andrea Page-McCaw

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 50 citations in OpenAlex.

  1. Macrophage restriction inScience advances · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Niche-derived exosomes controlFrontiers in immunology · 2026
    Article
  6. Article
  7. Article
  8. ALife science alliance · 2025
    Article
  9. Studying Cellular Senescence Using the Model Organism Drosophila melanogaster.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Hemocyte Clusters Defined by scRNA-Seq inFrontiers in immunology · 2022
    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

5 authors at 2 institutions in 1 country.

Kimberly S LaFeverDept. of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN, USA.
Xiaoxi WangDept. of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN, USA.
Patrick Page-McCawDept. of Molecular Physiology and Biophysics, Vanderbilt, University School of Medicine, Nashville, TN, USA.
Gautam BhaveDept. of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN, USA.
Andrea Page-McCawDept. of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN, USA.
Vanderbilt University Medical Center · USVanderbilt University · US

Funding

Matrix metalloproteinases in Drosophila wound healingR01GM073883 · NIGMS · VANDERBILT UNIVERSITY · PI PAGE-MCCAW, ANDREA · 2006 to 2015
$2.6M
Role of Peroxidasin in Glomerular Matrix HomeostasisK08DK097306 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BHAVE, GAUTAM · 2013 to 2017
$739k
NIDDK NIH HHS K08 DK097306NIGMS NIH HHS R01 GM073883Wellcome Trust
6 · The paper itself

Abstract

Matrix metalloproteinases (MMPs) are extracellular proteases that can cleave extracellular matrix and alter signaling pathways. They have been implicated in many disease states, but it has been difficult to understand the contribution of individual MMPs, as there are over 20 MMPs in vertebrates. The vertebrate MMPs have overlapping substrates, they exhibit genetic redundancy and compensation, and pharmacological inhibitors are non-specific. In contrast, there are only two MMP genes in Drosophila, DmMmp1 and DmMmp2, which makes Drosophila an attractive system to analyze the basis of MMP specificity. Previously, Drosophila MMPs have been categorized by their pericellular localization, as Mmp1 appeared to be secreted and Mmp2 appeared to be membrane-anchored, suggesting that protein localization was the critical distinction in this small MMP family. We report here that products of both genes are found at the cell surface and released into media. Additionally, we show that products of both genes contain GPI-anchors, and unexpectedly, that GPI-anchored MMPs promote cell adhesion when they are rendered inactive. Finally, by using new reagents and assays, we show that the two MMPs cleave different substrates, suggesting that this is the important distinction within this smallest MMP family.

Indexed as

AnimalsCell AdhesionCell MembraneDrosophila melanogasterExtracellular MatrixMatrix Metalloproteinase 1Matrix Metalloproteinase 2Signal TransductionSubstrate SpecificityMatrix Metalloproteinase 1Matrix Metalloproteinase 2

Identifiers

PMID28300207
PMCPMC5353688
OpenAlexW2595879941

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.