Evidence map›Paper›PMID 31043572›Full record

ArticleScience translational medicine2019

Nanofiber-hydrogel composite-mediated angiogenesis for soft tissue reconstruction.

Xiaowei Li, Brian Cho, Russell Martin, Michelle Seu, Chi Zhang, Zhengbing Zhou, Ji Suk Choi, Xuesong Jiang, Long Chen, Gurjot Walia and 9 more

Open access · greenAbstract read
In one paragraph

Article in Science translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
10.6field-weighted citation impact, top 1% 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

98 citing papers in PubMed, 241 citations in OpenAlex.

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38 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

19 authors at 1 institution in 1 country.

Xiaowei LiTranslational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0003-0714-1140
Brian ChoDepartment of Plastic and Reconstructive Surgery, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0001-6706-8390
Russell MartinTranslational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0002-6483-6005
Michelle SeuDepartment of Plastic and Reconstructive Surgery, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0002-6122-4767
Chi ZhangTranslational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0001-8201-3953
Zhengbing ZhouTranslational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.
Ji Suk ChoiTranslational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0002-7127-1858
Xuesong JiangTranslational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0002-6564-6190
Long ChenTranslational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0002-7347-3074
Gurjot WaliaDepartment of Plastic and Reconstructive Surgery, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0002-5212-0077
Jerry YanDepartment of Biomedical Engineering, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Megan CallananDepartment of Biomedical Engineering, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Huanhuan LiuTranslational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.
Kevin ColbertTranslational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0003-1594-5464
Justin Morrissette-McAlmonTranslational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.
Warren GraysonTranslational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.ORCID 0000-0001-6099-6469
Sashank ReddyDepartment of Plastic and Reconstructive Surgery, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA. hmao@jhu.edu jmsacks@jhmi.edu sreddy6@jhmi.edu.ORCID 0000-0001-6323-3950
Justin M SacksDepartment of Plastic and Reconstructive Surgery, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA. hmao@jhu.edu jmsacks@jhmi.edu sreddy6@jhmi.edu.
Hai-Quan MaoTranslational Tissue Engineering Center, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA. hmao@jhu.edu jmsacks@jhmi.edu sreddy6@jhmi.edu.ORCID 0000-0002-4262-9988
Johns Hopkins University · US

Funding

Promote Organization and Integration of Regenerated Neurons from Transplanted Human Neural Stem CellsR21NS096668 · NINDS · JOHNS HOPKINS UNIVERSITY · PI MAO, HAI-QUAN · 2017 to 2018
$450k
Directed In Vivo Differentiation of Neural Stem Cells for Repair of Brain LesionR21NS085714 · NINDS · JOHNS HOPKINS UNIVERSITY · PI MAO, HAI-QUAN · 2014 to 2015
$446k
NINDS NIH HHS R21 NS085714NINDS NIH HHS R21 NS096668
6 · The paper itself

Abstract

Soft tissue losses from tumor removal, trauma, aging, and congenital malformation affect millions of people each year. Existing options for soft tissue restoration have several drawbacks: Surgical options such as the use of autologous tissue flaps lead to donor site defects, prosthetic implants are prone to foreign body response leading to fibrosis, and fat grafting and dermal fillers are limited to small-volume defects and only provide transient volume restoration. In addition, large-volume fat grafting and other tissue-engineering attempts are hampered by poor vascular ingrowth. Currently, there are no off-the-shelf materials that can fill the volume lost in soft tissue defects while promoting early angiogenesis. Here, we report a nanofiber-hydrogel composite that addresses these issues. By incorporating interfacial bonding between electrospun poly(ε-caprolactone) fibers and a hyaluronic acid hydrogel network, we generated a composite that mimics the microarchitecture and mechanical properties of soft tissue extracellular matrix. Upon subcutaneous injection in a rat model, this composite permitted infiltration of host macrophages and conditioned them into the pro-regenerative phenotype. By secreting pro-angiogenic cytokines and growth factors, these polarized macrophages enabled gradual remodeling and replacement of the composite with vascularized soft tissue. Such host cell infiltration and angiogenesis were also observed in a rabbit model for repairing a soft tissue defect filled with the composite. This injectable nanofiber-hydrogel composite augments native tissue regenerative responses, thus enabling durable soft tissue restoration outcomes.

Indexed as

Neovascularization, PhysiologicTissue EngineeringAnimalsCell MovementCell PolarityDisease Models, AnimalGene Expression RegulationHydrogelsMacrophagesModels, AnimalNanofibersPhenotypeRabbitsRatsSubcutaneous TissueHydrogels

Identifiers

PMID31043572
PMCPMC12989237
OpenAlexW2942690026

What OpenQuestion holds

Textmetadata
LicenceTDM
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.