Evidence map›Paper›PMID 34222216›Full record

ArticleFrontiers in bioengineering and biotechnology2021

Magnetic Alignment of Electrospun Fiber Segments Within a Hydrogel Composite Guides Cell Spreading and Migration Phenotype Switching.

Harrison L Hiraki, Daniel L Matera, Michael J Rose, Robert N Kent, Connor W Todd, Mark E Stout, Anya E Wank, Maria C Schiavone, Samuel J DePalma, Alexander A Zarouk and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 36 citations in OpenAlex.

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  4. Electrospun Fibers EncapsulatingMolecules (Basel, Switzerland) · 2026
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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

11 authors at 1 institution in 1 country.

Harrison L HirakiDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, United States.
Daniel L MateraDepartment of Chemical Engineering, University of Michigan, Ann Arbor, MI, United States.
Michael J RoseDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, United States.
Robert N KentDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, United States.
Connor W ToddDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, United States.
Mark E StoutDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, United States.
Anya E WankDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, United States.
Maria C SchiavoneDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI, United States.
Samuel J DePalmaDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, United States.
Alexander A ZaroukDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, United States.
Brendon M BakerDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, United States.
University of Michigan–Ann Arbor · US

Funding

MICHIGAN MEDICAL SCIENTIST TRAINING PROGRAMT32GM007863 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COLLINS, KATHLEEN L. · 1985 to 2024
$38.3M
Tissue Engineering and RegenerationT32DE007057 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID H. KOHN · 1985 to 2026
$17.3M
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 EB030474NIDCR NIH HHS T32 DE007057NIGMS NIH HHS T32 GM007863
6 · The paper itself

Abstract

Fibrous extracellular matrix (ECM) proteins provide mechanical structure and adhesive scaffolding to resident cells within stromal tissues. Aligned ECM fibers play an important role in directing morphogenetic processes, supporting mechanical loads, and facilitating cell migration. Various methods have been developed to align matrix fibers in purified biopolymer hydrogels, such as type I collagen, including flow-induced alignment, uniaxial tensile deformation, and magnetic particles. However, purified biopolymers have limited orthogonal tunability of biophysical cues including stiffness, fiber density, and fiber alignment. Here, we generate synthetic, cell-adhesive fiber segments of the same length-scale as stromal fibrous proteins through electrospinning. Superparamagnetic iron oxide nanoparticles (SPIONs) embedded in synthetic fiber segments enable magnetic field induced alignment of fibers within an amorphous bulk hydrogel. We find that SPION density and magnetic field strength jointly influence fiber alignment and identify conditions to control the degree of alignment. Tuning fiber length allowed the alignment of dense fibrous hydrogel composites without fiber entanglement or regional variation in the degree of alignment. Functionalization of fiber segments with cell adhesive peptides induced tendon fibroblasts to adopt a uniaxial morphology akin to within native tendon. Furthermore, we demonstrate the utility of this hydrogel composite to direct multicellular migration from MCF10A spheroids and find that fiber alignment prompts invading multicellular strands to separate into disconnected single cells and multicellular clusters. These magnetic fiber segments can be readily incorporated into other natural and synthetic hydrogels and aligned with inexpensive and easily accessible rare earth magnets, without the need for specialized equipment. 3D hydrogel composites where stiffness/crosslinking, fiber density, and fiber alignment can be orthogonally tuned may provide insights into morphogenetic and pathogenic processes that involve matrix fiber alignment and can enable systematic investigation of the individual contribution of each biophysical cue to cell behavior.

Indexed as

electrospinningepithelial cell migrationfiber alignmenthydrogeltendon

Identifiers

PMID34222216
PMCPMC8242362
OpenAlexW3170572495

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.