Evidence map›Paper›PMID 38088893›Full record

ArticleMolecular biology of the cell2024

Macrophage migration is differentially regulated by fibronectin and laminin through altered adhesion and myosin II localization.

Matthew W Stinson, Sophia Liu, Alexander J Laurenson, Jeremy D Rotty

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 15 citations in OpenAlex.

  1. Blocking the mCellular & molecular immunology · 2026
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  11. The Arp2/3 complex is required forbioRxiv : the preprint server for biology · 2025
    Article
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  14. Review
  15. Article
  16. Progress in macrophage immune regulation of atherosclerosis.American journal of translational research · 2025
    Review
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Matthew W StinsonUniformed Services University of the Health Sciences, Department of Biochemistry, Bethesda, MD 20814.
Sophia LiuUniformed Services University of the Health Sciences, Department of Biochemistry, Bethesda, MD 20814.
Alexander J LaurensonUniformed Services University of the Health Sciences, Department of Biochemistry, Bethesda, MD 20814.
Jeremy D RottyUniformed Services University of the Health Sciences, Department of Biochemistry, Bethesda, MD 20814.
Henry M. Jackson Foundation · USUniformed Services University of the Health Sciences · US

Funding

Extracellular matrix sensing in cellular signaling, migration and wound repairR01GM134104 · NIGMS · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI ROTTY, JEREMY · 2019 to 2023
$1.6M
NIGMS NIH HHS R01 GM134104
6 · The paper itself

Abstract

Macrophages are indispensable for proper immune surveillance and inflammatory regulation. They also exhibit dramatic phenotypic plasticity and are highly responsive to their local microenvironment, which includes the extracellular matrix (ECM). This work demonstrates that two fibrous ECM glycoproteins, fibronectin (FN) and laminin (LAM), elicit distinct morphological and migratory responses from macrophages in two-dimensional environments. LAM 111 inhibits macrophage cell spreading, but drives them to migrate rapidly and less persistently compared with cells on FN. Differential integrin engagement and ROCK/myosin II organization helps explain why macrophages alter their morphology and migration character on these two ECM components. This study also demonstrates that LAM 111 exerts a suppressive effect toward FN, as macrophages plated on a LAM/FN mixture adopt a morphology and migratory character almost identical to LAM alone. This suggests that distinct responses can be initiated downstream of receptor-ECM engagement, and that one component of the microenvironment may affect the cell's ability to sense another. Overall, macrophages appear intrinsically poised to rapidly switch between distinct migratory characters based on their ECM environments. The role of ECM composition in dictating motile and inflammatory responses in three-dimensional and in vivo contexts warrants further study.

Indexed as

Extracellular MatrixFibronectinsCell AdhesionCell MovementCytoskeletal ProteinsLamininMacrophagesMyosin Type IICytoskeletal ProteinsFibronectinsLamininMyosin Type II

Identifiers

PMID38088893
PMCPMC10881148
OpenAlexW4389671097

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.