Evidence map›Paper›PMID 31297910›Full record

ArticleCell proliferation2019

Enhanced bone tissue regeneration of a biomimetic cellular scaffold with co-cultured MSCs-derived osteogenic and angiogenic cells.

Limei Li, Jidong Li, Qin Zou, Yi Zuo, Bin Cai, Yubao Li

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 36 citations in OpenAlex.

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  13. Educating EVs to Improve Bone Regeneration: Getting Closer to the Clinic.International journal of molecular sciences · 2022
    Review
  14. Bone Regeneration and Oxidative Stress: An Updated Overview.Antioxidants (Basel, Switzerland) · 2022
    Review
  15. 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

6 authors at 1 institution in 1 country.

Limei LiResearch Center for Nano-Biomaterials, Analytical & Testing Center, Sichuan University, Chengdu, China.ORCID https://orcid.org/0000-0001-8547-0711
Jidong LiResearch Center for Nano-Biomaterials, Analytical & Testing Center, Sichuan University, Chengdu, China.
Qin ZouResearch Center for Nano-Biomaterials, Analytical & Testing Center, Sichuan University, Chengdu, China.
Yi ZuoResearch Center for Nano-Biomaterials, Analytical & Testing Center, Sichuan University, Chengdu, China.
Bin CaiResearch Center for Nano-Biomaterials, Analytical & Testing Center, Sichuan University, Chengdu, China.
Yubao LiResearch Center for Nano-Biomaterials, Analytical & Testing Center, Sichuan University, Chengdu, China.
Sichuan University · CN

Funding

Key Applied Basic Research Program of Sichuan Province 2018JY0031National Key Research and Development Program of China 2016YFA0201703/2016YFA0201700NFSC fund 31670965/81860326
6 · The paper itself

Abstract

objectivesThe bone tissue engineering primarily focuses on three-dimensional co-culture systems, which physical and biological properties resemble the cell matrix of actual tissues. The complex dialogue between bone-forming and endothelial cells (ECs) in a tissue-engineered construct will directly regulate angiogenesis and bone regeneration. The purpose of this study was to investigate whether co-culture between osteogenic and angiogenic cells derived by bone mesenchymal stem cells (MSCs) could affect cell activities and new bone formation. MATERIALS AND

methodsMesenchymal stem cells were dually induced to differentiate into osteogenic cells (OMSCs) and ECs; both cell types were co-cultured at different ratios to investigate their effects and underlying mechanisms through ELISA, RT-qPCR and MTT assays. The selected cell mixture was transplanted onto a nano-hydroxyapatite/polyurethane (n-HA/PU) scaffold to form a cell-scaffold construct that was implanted in the rat femoral condyles. Histology and micro-CT were examined for further verification.

resultsELISA and gene expression studies revealed that co-cultured OMSCs/ECs (0.5/1.5) significantly elevated the transcription levels of osteogenic genes such as ALP, Col-I and OCN, as well as transcription factors Msx2, Runx2 and Osterix; it also upregulated angiogenic factors of vascular endothelial growth factor (VEGF) and CD31 when compared with cells cultured alone or in other ratios. The optimized OMSCs/ECs group had more abundant calcium phosphate crystal deposition, further facilitated their bone formation in vivo.

conclusionsThe OMSCs/ECs-scaffold constructs at an optimal cell ratio (0.5/1.5) achieved enhanced osteogenic and angiogenic factor expression and biomineralization, which resulted in more effective bone formation.

Indexed as

AnimalsBiomimetic MaterialsBone and BonesBone RegenerationCell DifferentiationCells, CulturedCoculture TechniquesCore Binding Factor Alpha 1 SubunitDurapatiteEndothelial CellsMesenchymal Stem CellsMesenchymal Stem Cell TransplantationOsteogenesisRatsRats, Sprague-DawleyTissue EngineeringCore Binding Factor Alpha 1 SubunitDurapatiteRunx2 protein, ratSp7 protein, ratTranscription FactorsVascular Endothelial Growth Factor Aangiogenic cellsbiomimetic scaffoldbone tissue engineeringco-cultureosteogenesisstem cells

Identifiers

PMID31297910
PMCPMC6797511
OpenAlexW2956852424

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.