Evidence map›Paper›PMID 28358890›Full record

ArticlePloS one2017

A multifunctional bioactive material that stimulates osteogenesis and promotes the vascularization bone marrow stem cells and their resistance to bacterial infection.

Chuang Ma, Qin Wei, Bo Cao, Xinchun Cheng, Juling Tian, Hongwei Pu, Aihemaitijiang Yusufu, Li Cao

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

6 citing papers in PubMed, 19 citations in OpenAlex.

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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

8 authors at 4 institutions in 1 country.

Chuang MaDepartment of Orthopedics Center, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Qin WeiXinjiang Key Laboratory of Medical Animal Model Research, Clinical Medical Research Institute of the First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Bo CaoDepartment of Orthopedics Center, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Xinchun ChengCarders Health Care No. 4 Department of Xinjiang Uygur Autonomous Region People's Hospital, Urumqi, China.
Juling TianDepartment of Clinical Laboratory, The first people's Hospital of Urumqi, Urumqi, China.
Hongwei PuDepartment of Science and Research Education Center, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Aihemaitijiang YusufuDepartment of Orthopedics Center, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Li CaoDepartment of Orthopedics Center, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Xinjiang Medical University · CNFirst Affiliated Hospital of Xinjiang Medical University · CNPeople's Hospital of Xinjiang Uygur Autonomous Region · CNUrumqi 4th People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The main limitation of tissue engineering lies in the inability to stimulate osteogenesis, angiogenesis of stem cells and broad-spectrum antimicrobial activity. However, the development of multifunctional bioactive materials with these capabilities remains a great challenge. In this study, we prepared mesoporous silica nanoparticles encapsulated with silver nanocrystals (AG-MSN) with uniform sphere size and mesopores. Platelet-derived growth factor BB (PDGF-BB) was effectively loaded in the AG-MSN mesopores (P-AG-MSN). The silicon ions (Si) released by P-AG-MSN stimulate osteogenic differentiation of bone marrow stromal cells (BMSC) by activating the alkaline phosphatase (ALP) activity of bone-related genes and increasing protein (OCN, RUNX2 and OPN) expression. Ag+ ions could be slowly released from the interior of the shell, highlighting their durable antibacterial activity. The sustained release of PDGF-BB from P-AG-MSN stimulated the angiogenic differentiation of BMSC, as indicated by the enhanced secretion of vascular endothelial growth factor (VEGF), HIF-1α, HGF and ANG-1 and protein expression. Our results show that P-AG-MSN can clearly promote BMSC osteostimulation and vascularization. This research serves as a preliminary study of the utilization of this multifunctional mixture to fabricate a new active biological scaffold that integrates BMSC osteostimulation, vascularization and bactericidal effects by 3D printing technology.

Indexed as

Bacterial InfectionsBecaplerminBone Marrow CellsCell DifferentiationGene Expression Regulation, DevelopmentalHematopoietic Stem CellsHepatocyte Growth FactorHumansHypoxia-Inducible Factor 1, alpha SubunitNanoparticlesNeovascularization, PhysiologicOsteogenesisPrinting, Three-DimensionalProto-Oncogene Proteins c-sisRibonuclease, PancreaticSilicon DioxideangiogeninBecaplerminHepatocyte Growth FactorHGF protein, humanHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitProto-Oncogene Proteins c-sisRibonuclease, PancreaticSilicon DioxideVascular Endothelial Growth Factor A

Identifiers

PMID28358890
PMCPMC5373515
OpenAlexW2599907416

What OpenQuestion holds

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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.