Evidence map›Paper›PMID 32585131›Full record

ArticleDevelopmental cell2020

Rapid Homeostatic Turnover of Embryonic ECM during Tissue Morphogenesis.

Yutaka Matsubayashi, Besaiz Jose Sánchez-Sánchez, Stefania Marcotti, Eduardo Serna-Morales, Anca Dragu, María-Del-Carmen Díaz-de-la-Loza, Gema Vizcay-Barrena, Roland Alexander Fleck, Brian Marc Stramer

Open access · hybridAbstract read
In one paragraph

Article in Developmental cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. The Role ofBiology · 2025
    Article
  12. Basement membranes at a glance.Journal of cell science · 2025
    Review
  13. The life cycle of type IV collagen.Matrix biology : journal of the International Society for Matrix Biology · 2025
    Review
  14. Beyond classical collagen: basement membrane collagen IV in age-associated lung diseases.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Yutaka MatsubayashiRandall Centre for Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK. Electronic address: yutaka.matsubayashi@kcl.ac.uk.
Besaiz Jose Sánchez-SánchezRandall Centre for Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK.
Stefania MarcottiRandall Centre for Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK.
Eduardo Serna-MoralesRandall Centre for Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK.
Anca DraguRandall Centre for Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK.
María-Del-Carmen Díaz-de-la-LozaRandall Centre for Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK.
Gema Vizcay-BarrenaCentre for Ultrastructure Imaging, King's College London, London SE1 1UL, UK.
Roland Alexander FleckCentre for Ultrastructure Imaging, King's College London, London SE1 1UL, UK.
Brian Marc StramerRandall Centre for Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK. Electronic address: brian.m.stramer@kcl.ac.uk.
King's College London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/F020635/2European Research Council 681808Wellcome Trust 107859/Z/15/Z
6 · The paper itself

Abstract

The extracellular matrix (ECM) is a polymer network hypothesized to form a stable cellular scaffold. While the ECM can undergo acute remodeling during embryogenesis, it is experimentally difficult to determine whether basal turnover is also important. Most studies of homeostatic turnover assume an initial steady-state balance of production and degradation and measure half-life by quantifying the rate of decay after experimental intervention (e.g., pulse labeling). Here, we present an intervention-free approach to mathematically model basal ECM turnover during embryogenesis by exploiting our ability to live image de novo ECM development in Drosophila to quantify production from initiation to homeostasis. This reveals rapid turnover (half-life ∼7-10 h), which we confirmed by in vivo pulse-chase experiments. Moreover, ECM turnover is partially dependent on proteolysis and network interactions, and slowing turnover affects tissue morphogenesis. These data demonstrate that embryonic ECM undergoes constant replacement, which is likely necessary to maintain network plasticity to accommodate growth and morphogenesis.

Indexed as

HomeostasisMorphogenesisAnimalsBasement MembraneDrosophila melanogasterDrosophila ProteinsEpithelial CellsExtracellular MatrixExtracellular Matrix ProteinsModels, TheoreticalDrosophila ProteinsExtracellular Matrix Proteinsbasement membraneCollagenembryogenesisextracellular matrixmathematical modelingMatrix metalloproteasemorphogenesisNidogenPerlecanturnover

Identifiers

PMID32585131
PMCPMC7332994
OpenAlexW3037242948

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.