Evidence map›Paper›PMID 30464457›Full record

ArticleInternational journal of nanomedicine2018

Inverse opal substrate-loaded mesenchymal stem cells contribute to decreased myocardial remodeling after transplantation into acute myocardial infarction mice.

Wenbin Lu, JingJing Ji, Genshan Ma, Qiming Dai, Lijuan Chen, Pengfei Zuo, Yuanjin Zhao

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Guarana (Paullinia cupana) as a potential tool for mesenchymal stromal cells priming in regenerative medicine.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    Article
  4. MSCs Contribute to the Conversion of Ly6CStem cells international · 2020
    Article
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

7 authors.

Wenbin LuDepartment of Cardiology, ZhongDa Hospital Affiliated with Southeast University, Nanjing, China, luwenbinseu@163.com.
JingJing JiDepartment of Cardiology, ZhongDa Hospital Affiliated with Southeast University, Nanjing, China, luwenbinseu@163.com.
Genshan MaDepartment of Cardiology, ZhongDa Hospital Affiliated with Southeast University, Nanjing, China, luwenbinseu@163.com.
Qiming DaiDepartment of Cardiology, ZhongDa Hospital Affiliated with Southeast University, Nanjing, China, luwenbinseu@163.com.
Lijuan ChenDepartment of Cardiology, ZhongDa Hospital Affiliated with Southeast University, Nanjing, China, luwenbinseu@163.com.
Pengfei ZuoDepartment of Cardiology, ZhongDa Hospital Affiliated with Southeast University, Nanjing, China, luwenbinseu@163.com.
Yuanjin ZhaoState Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing, China, yjzhao@seu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe two-dimensional incubation method is now the most commonly method for mesenchymal stem cell (MSC) production. however, gene expression and secretion of growth factors are relatively low; thus, the transplanted cells cannot be effectively utilized for potential clinical applications after acute myocardial infarction (AMI).

objectivesWe aimed to investigate whether our newly made substrates of inverse opal with specific surface microstructures for MSC culturing can increase the viability of the cells and can contributes to decreased myocardial remodeling after transplanted to AMI mice.

methodsThe inverse opal structure is fabricated by the convenient bottom-up approach of the self-assembly of colloidal nanoparticles. Mouse-derived MSCs were then cultured on the substrates when expanded at different times to investigate the cell growth status including morphology. Then the inverse opal substrates loaded MSCs were transplanted to AMI mice, cardiomyocyte apoptosis and LV remodeling were further compared. To explore the possible mechanisms of curation, the secretions and viability of MSCs on substrates were determined using mice ELISA kits and JC-1 mitochondrial membrane potential assay kits respectively at normal and hypoxic conditions.

results6 times expanded inverse opals allowed greatly the orderly growth of MSCs as compared to four (34% ± 10.6%) and two (20%±7.2%) times expanded as well as unexpanded (13%±4.1%) (

conclusionThe structure of inverse opal can not only adjust the arrangement of MSCs but also contribute to its orientated growth. Inverse opal loaded MSCs transplantation extremely curbed myocardial remodeling, the underlying mechanisms might be the high viability and extremely higher secretions of growth factors of MSCs as devoted by this method.

Indexed as

Mesenchymal Stem Cell TransplantationVentricular RemodelingAnimalsApoptosisCell ProliferationCells, CulturedCell SurvivalIntercellular Signaling Peptides and ProteinsMesenchymal Stem CellsMice, Inbred BALB CMyocardial InfarctionMyocardiumNanoparticlesIntercellular Signaling Peptides and ProteinsAMIinverse opalMSCs

Identifiers

PMID30464457
PMCPMC6220438

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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.