Evidence map›Paper›PMID 30154864›Full record

ArticleStem cells international2018

Combining PLGA Scaffold and MSCs for Brain Tissue Engineering: A Potential Tool for Treatment of Brain Injury.

Ling Zhou, Jiangyi Tu, Guangbi Fang, Li Deng, Xiaoqing Gao, Kan Guo, Jiming Kong, Jing Lv, Weikang Guan, Chaoxian Yang

Open access · goldAbstract read
In one paragraph

Article in Stem cells international, 2018. 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
3.8field-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

17 citing papers in PubMed, 36 citations in OpenAlex.

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  10. Article
  11. Biomaterial-Assisted Regenerative Medicine.International journal of molecular sciences · 2021
    Review
  12. Article
  13. Article
  14. RepositioningPharmaceutics · 2020
    Article
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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

10 authors at 2 institutions in 2 countries.

Ling ZhouDepartment of Endocrinology, The Affiliated Hospital, Southwest Medical University, Taiping Street, Luzhou 646000, China.
Jiangyi TuDepartment of Anatomy, Southwest Medical University, Zhongshan Road, Luzhou 646000, China.
Guangbi FangDepartment of Anatomy, Southwest Medical University, Zhongshan Road, Luzhou 646000, China.
Li DengDepartment of Anatomy, Southwest Medical University, Zhongshan Road, Luzhou 646000, China.
Xiaoqing GaoDepartment of Anatomy, Southwest Medical University, Zhongshan Road, Luzhou 646000, China.ORCID 0000-0003-2000-6269
Kan GuoDepartment of Neurobiology, Preclinical Medicine Research Center, Southwest Medical University, Zhongshan Road, Luzhou 646000, China.
Jiming KongDepartment of Human Anatomy and Cell Science, College of Medicine, University of Manitoba, Winnipeg, MB, Canada.
Jing LvDepartment of Neurobiology, Preclinical Medicine Research Center, Southwest Medical University, Zhongshan Road, Luzhou 646000, China.
Weikang GuanDepartment of Neurobiology, Preclinical Medicine Research Center, Southwest Medical University, Zhongshan Road, Luzhou 646000, China.
Chaoxian YangDepartment of Anatomy, Southwest Medical University, Zhongshan Road, Luzhou 646000, China.ORCID 0000-0002-7462-6423
Southwest Medical University · CNUniversity of Manitoba · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nerve tissue engineering is an important strategy for the treatment of brain injuries. Mesenchymal stem cell (MSC) transplantation has been proven to be able to promote repair and functional recovery of brain damage, and poly (lactic-co-glycolic acid) (PLGA) has also been found to have the capability of bearing cells. In the present study, to observe the ability of PLGA scaffold in supporting the adherent growth of MSCs and neurons in vivo and vitro and to assess the effects of PLGA scaffold on proliferation and neural differentiation of MSCs, this study undertakes the following steps. First, MSCs and neurons were cultured and labeled with green fluorescent protein (GFP) or otherwise identified and the PLGA scaffold was synthesized. Next, MSCs and neurons were inoculated on PLGA scaffolds and their adhesion rates were investigated and the proliferation of MSCs was evaluated by using MTT assay. After MSCs were induced by a neural induction medium, the morphological change and neural differentiation of MSCs were detected using scanning electron microscopy (SEM) and immunocytochemistry, respectively. Finally, cell migration and adhesion in the PLGA scaffold in vivo were examined by immunohistochemistry, nuclear staining, and SEM. The experimental results demonstrated that PLGA did not interfere with the proliferation and neural differentiation of MSCs and that MSCs and neuron could grow and migrate in PLGA scaffold. These data suggest that the MSC-PLGA complex may be used as tissue engineering material for brain injuries.

Identifiers

PMID30154864
PMCPMC6098877
OpenAlexW2887771037

What OpenQuestion holds

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LicenceCC BY
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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.