Evidence map›Paper›PMID 34777599›Full record

ArticleCellular and molecular bioengineering2021

The Role of Rho GTPases During Fibroblast Spreading, Migration, and Myofibroblast Differentiation in 3D Synthetic Fibrous Matrices.

Daniel L Matera, Alexander T Lee, Harrison L Hiraki, Brendon M Baker

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular bioengineering, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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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.

Daniel L MateraDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI 48109 USA.
Alexander T LeeDepartment of Biology, University of Michigan, Ann Arbor, MI 48109 USA.
Harrison L HirakiDepartment of Biomedical Engineering, University of Michigan, 2174 Lurie BME Building, 1101 Beal Avenue, Ann Arbor, MI 48109 USA.
Brendon M BakerDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI 48109 USA.ORCID 0000-0002-2785-1070
University of Michigan · US

Funding

Angiogenic hydrogel composites for microvascular integration of organoid graftsR01EB030474 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BAKER, BRENDON M · 2021 to 2024
$1.4M
Mechanics of fibrosis in 3D biomimetic extracellular matricesR00HL124322 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BAKER, BRENDON M · 2017 to 2019
$747k
Mechanics of fibrosis in 3D biomimetic extracellular matricesK99HL124322 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI BAKER, BRENDON M · 2015 to 2016
$261k
NHLBI NIH HHS K99 HL124322NHLBI NIH HHS R00 HL124322NIBIB NIH HHS R01 EB030474
6 · The paper itself

Abstract

introductionConnective tissue repair and mechanosensing are tightly entwined

methodsWe employed a 3D, fibrous and protease-sensitive hydrogel model of interstitial ECM to study the interplay between Rho GTPases and fibrous matrix cues in fibroblasts during wound healing.

resultsModulating fiber density within protease-sensitive hydrogels, we confirmed previous findings that heightened fiber density promotes fibroblast spreading and proliferation. The presence of matrix fibers furthermore corresponded to increased cell migration speeds and macroscopic hydrogel contraction arising from fibroblast generated forces. During fibroblast spreading, Rac1 and RhoA GTPase activity proved crucial for fiber-mediated cell spreading and contact guidance along matrix fibers, while Cdc42 was dispensable. In contrast, interplay between RhoA, Rac1, and Cdc42 contributed to fiber-mediated myofibroblast differentiation and matrix contraction over longer time scales.

conclusionThese observations may provide insights into tissue repair processes in vivo and motivate the incorporation of cell-adhesive fibers within synthetic hydrogels for material-guided wound repair strategies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12195-021-00698-5.

Indexed as

Cell migrationElectrospinningExtracellular matrixFibersFibroblastMechanosensingMicroenvironmentMyofibroblastRho GTPaseSynthetic hydrogelsWound healing

Identifiers

PMID34777599
PMCPMC8548490
OpenAlexW3196298188

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.