Evidence map›Paper›PMID 33417803›Full record

ArticleACS biomaterials science & engineering2019

Fabrication and Characterization of Pectin Hydrogel Nanofiber Scaffolds for Differentiation of Mesenchymal Stem Cells into Vascular Cells.

Na Li, Fuxin Xue, Hui Zhang, Hanna J Sanyour, Alex P Rickel, Andrew Uttecht, Betty Fanta, Junli Hu, Zhongkui Hong

Open access · greenAbstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 74 citations in OpenAlex.

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  17. Electrospun nanofiber scaffold for vascular tissue engineering.Materials science & engineering. C, Materials for biological applications · 2021
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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

9 authors at 2 institutions in 2 countries.

Na LiDepartment of Biomedical Engineering, University of South Dakota, Sioux Falls, South Dakota 57107, United States.
Fuxin XueKey Laboratory of UV-Emitting Materials and Technology (Northeast Normal University), Ministry of Education, Changchun, Jilin 130024, P. R. China.
Hui ZhangKey Laboratory of UV-Emitting Materials and Technology (Northeast Normal University), Ministry of Education, Changchun, Jilin 130024, P. R. China.
Hanna J SanyourDepartment of Biomedical Engineering, University of South Dakota, Sioux Falls, South Dakota 57107, United States.ORCID http://orcid.org/0000-0003-3254-8807
Alex P RickelDepartment of Biomedical Engineering, University of South Dakota, Sioux Falls, South Dakota 57107, United States.
Andrew UttechtDepartment of Biomedical Engineering, University of South Dakota, Sioux Falls, South Dakota 57107, United States.
Betty FantaDepartment of Biomedical Engineering, University of South Dakota, Sioux Falls, South Dakota 57107, United States.
Junli HuKey Laboratory of UV-Emitting Materials and Technology (Northeast Normal University), Ministry of Education, Changchun, Jilin 130024, P. R. China.ORCID http://orcid.org/0000-0002-4715-7377
Zhongkui HongDepartment of Biomedical Engineering, University of South Dakota, Sioux Falls, South Dakota 57107, United States.ORCID http://orcid.org/0000-0003-1745-6488
University of South Dakota · USNortheast Normal University · CN

Funding

American Heart Association-American Stroke Association 15SDG25420001
6 · The paper itself

Abstract

Despite significant progress over the past few decades, creating a tissue-engineered vascular graft with replicated functions of native blood vessels remains a challenge due to the mismatch in mechanical properties, low biological function, and rapid occlusion caused by restenosis of small diameter vessel grafts (<6 mm diameter). A scaffold with similar mechanical properties and biocompatibility to the host tissue is ideally needed for the attachment and proliferation of cells to support the building of engineered tissue. In this study, pectin hydrogel nanofiber scaffolds with two different oxidation degrees (25 and 50%) were prepared by a multistep methodology including periodate oxidation, electrospinning, and adipic acid dihydrazide crosslinking. Scanning electron microscopy (SEM) images showed that the obtained pectin nanofiber mats have a nano-sized fibrous structure with 300-400 nm fiber diameter. Physicochemical property testing using Fourier transform infrared (FTIR) spectra, atomic force microscopy (AFM) nanoindentations, and contact angle measurements demonstrated that the stiffness and hydrophobicity of the fiber mat could be manipulated by adjusting the oxidation and crosslinking levels of the pectin hydrogels. Live/Dead staining showed high viability of the mesenchymal stem cells (MSCs) cultured on the pectin hydrogel fiber scaffold for 14 days. In addition, the potential application of pectin hydrogel nanofiber scaffolds of different stiffness in stem cell differentiation into vascular cells was assessed by gene expression analysis. Real-time polymerase chain reaction (RT-PCR) results showed that the stiffer scaffold facilitated the differentiation of MSCs into vascular smooth muscle cells, while the softer fiber mat promoted MSC differentiation into endothelial cells. Altogether, our results indicate that the pectin hydrogel nanofibers have the capability of providing mechanical cues that induce MSC differentiation into vascular cells and can be potentially applied in stem cell-based tissue engineering.

Indexed as

electrospinhydrogelmesenchymal stem cellpectinscaffoldvascular cells

Identifiers

PMID33417803
PMCPMC11268401
OpenAlexW2982335880

What OpenQuestion holds

Textmetadata
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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.