Evidence map›Paper›PMID 18495809›Full record

ArticleAmerican journal of physiology. Cell physiology2008

Extracellular matrix-specific focal adhesions in vascular smooth muscle produce mechanically active adhesion sites.

Zhe Sun, Luis A Martinez-Lemus, Michael A Hill, Gerald A Meininger

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

64 citing papers in PubMed, 127 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Vascular mechanotransduction.Physiological reviews · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Biomechanical signal communication in vascular smooth muscle cells.Journal of cell communication and signaling · 2020
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

4 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Zhe SunDalton Cardiovascular Research Center, University of Missouri, Columbia, MO 65211, USA.
Luis A Martinez-Lemus
Michael A Hill
Gerald A Meininger
University of Missouri · US

Funding

MICROVASCULAR CONTROL--A ROLE FOR INTEGRINSR01HL058690 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI MEININGER, GERALD A. · 1998 to 2007
$2.0M
HYPERTENSION AND ARTERIAL INJURY--A ROLE FOR INTEGRINSR01HL062863 · NHLBI · TEXAS ENGINEERING EXPERIMENT STATION · PI MEININGER, GERALD A. · 1999 to 2002
$864k
CATCH--A STUDY OF INSTITUTIONALIZATIONR01HL058960 · NHLBI · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI NADER, PHILIP R · 1998 to 1999
–
NHLBI NIH HHS HL 062863NHLBI NIH HHS HL 58960NHLBI NIH HHS R01 HL058690
6 · The paper itself

Abstract

Integrin-mediated mechanotransduction in vascular smooth muscle cells (VSMCs) plays an important role in the physiological control of tissue blood flow and vascular resistance. To test whether force applied to specific extracellular matrix (ECM)-integrin interactions could induce myogenic-like mechanical activity at focal adhesion sites, we used atomic force microscopy (AFM) to apply controlled forces to specific ECM adhesion sites on arteriolar VSMCs. The tip of AFM probes were fused with a borosilicate bead (2 ~ 5 microm) coated with fibronectin (FN), collagen type I (CNI), laminin (LN), or vitronectin (VN). ECM-coated beads induced clustering of alpha(5)- and beta(3)-integrins and actin filaments at sites of bead-cell contact indicative of focal adhesion formation. Step increases of an upward (z-axis) pulling force (800 ~ 1,600 pN) applied to the bead-cell contact site for FN-specific focal adhesions induced a myogenic-like, force-generating response from the VSMC, resulting in a counteracting downward pull by the cell. This micromechanical event was blocked by cytochalasin D but was enhanced by jasplakinolide. Function-blocking antibodies to alpha(5)beta(1)- and alpha(v)beta(3)-integrins also blocked the micromechanical cell event in a concentration-dependent manner. Similar pulling experiments with CNI, VN, or LN failed to induce myogenic-like micromechanical events. Collectively, these results demonstrate that mechanical force applied to integrin-FN adhesion sites induces an actin-dependent, myogenic-like, micromechanical event. Focal adhesions formed by different ECM proteins exhibit different mechanical characteristics, and FN appears of particular relevance in its ability to strongly attach to VSMCs and to induce myogenic-like, force-generating reactions from sites of focal adhesion in response to externally applied forces.

Indexed as

AnimalsCells, CulturedCollagen Type ICytochalasinsDepsipeptidesExtracellular MatrixFocal AdhesionsIntegrin alpha5beta1Integrin alphaVbeta3LamininMicrocirculationMicroscopy, Atomic ForceMuscle, Smooth, VascularMyocytes, Smooth MuscleRatsRats, Sprague-DawleyCollagen Type Icytochalasin ACytochalasinsDepsipeptidesIntegrin alpha5beta1Integrin alphaVbeta3jasplakinolideLamininVitronectin

Identifiers

PMID18495809
PMCPMC2493553
OpenAlexW2125047490

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.