Evidence map›Paper›PMID 8590805›Full record

ArticleMolecular biology of the cell1995

Cell adhesion to extracellular matrix regulates the life cycle of integrins.

S L Dalton, E Scharf, R Briesewitz, E E Marcantonio, R K Assoian

Open access · greenAbstract readComparative Study
In one paragraph

Article in Molecular biology of the cell, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The roles of ADAMTS in angiogenesis and cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Review
  6. Article
  7. Article
  8. Neural tissue continues its maturation at the site of neural tube closure defects: implications for prenatal intervention in human samples.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2004
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Signaling via beta1 integrins and mitogen-activated protein kinase determines human epidermal stem cell fate in vitro.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  14. Article
  15. 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 1 institution in 1 country.

S L DaltonDepartment of Cell Biology and Anatomy, University of Miami School of Medicine, Florida 33101, USA.
E Scharf
R Briesewitz
E E Marcantonio
R K Assoian
University of Miami · US

Funding

CELL CYCLE CONTROL BY INTEGRINSR01GM051878 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI ASSOIAN, RICHARD · 1995 to 2004
$1.2M
STRUCTURE/FUNCTION OF THE INTEGRIN ALPHA 1 BETA 1R01GM044585 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI MARCANTONIO, EUGENE E. · 1990 to 2002
$1.1M
NIGMS NIH HHS GM-07367NIGMS NIH HHS GM-44585NIGMS NIH HHS GM-51878
6 · The paper itself

Abstract

The expression of alpha 5 beta 1 integrin on the surface of fibroblasts requires adhesion to substratum. We have examined the basis for this adhesion-dependent surface expression by comparing the life cycle of integrins in parallel cultures of adherent and nonadherent cells. Results of biosynthetic labeling experiments in NRK fibroblasts showed that the synthesis and biosynthetic processing of the beta 1 integrin subunit proceed in the absence of cell attachment; however, when examining the behavior of preexisting cell surface integrins, we observed that the alpha beta 1 integrins are internalized and degraded when adhesion to substratum is blocked. A kinetic analysis of integrin internalization in cycloheximide-treated NRK cells showed that each of the fibroblast integrins we examined (in both the beta 1 and beta 3 families) are lost from the cell surface after detachment from substratum. Thus, the default integrin life cycle in fibroblasts involves continuous synthesis, processing, transport to the cell surface, and internalization/degradation. Interestingly, studies with NIH-3T3 cells expressing alpha 1 beta 1 integrin showed that the loss of cell-surface alpha 5 beta 1 integrin is blocked by adhesion of cells to dishes coated with type IV collagen (a ligand for alpha 1 beta 1 integrin) as well as fibronectin. Similarly, adhesion of these cells to dishes coated with type IV collagen stabilizes the surface expression of alpha 5 beta 1 as well as alpha 1 beta 1 integrin. We propose that the adhesion of fibroblasts to extracellular matrix protein alters the integrin life cycle and permits retention of these proteins at the cell surface where they can play important roles in transmitting adhesion-dependent signals.

Indexed as

Cell Adhesion3T3 CellsAnimalsAntigens, CDCell LineCycloheximideExtracellular MatrixFibroblastsHomeostasisIntegrin alphaVIntegrin beta1Integrin beta3IntegrinsKidneyKineticsMiceAntigens, CDCycloheximideIntegrin alphaVIntegrin beta1Integrin beta3IntegrinsPlatelet Membrane GlycoproteinsProtein Synthesis Inhibitors

Identifiers

PMID8590805
PMCPMC301332
OpenAlexW2106726165

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.