Evidence map›Paper›PMID 25630903›Full record

ArticleJournal of biomedical materials research. Part A2015

Human periosteum cell osteogenic differentiation enhanced by ionic silicon release from porous amorphous silica fibrous scaffolds.

Tetsurou Odatsu, Taha Azimaie, Megan F Velten, Michael Vu, Mark B Lyles, Harry K Kim, Pranesh B Aswath, Venu G Varanasi

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.4field-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

8 citing papers in PubMed, 31 citations in OpenAlex.

  1. SiONAntioxidants (Basel, Switzerland) · 2024
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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 3 institutions in 2 countries.

Tetsurou OdatsuDepartment of Biomedical Sciences, Baylor College of Dentistry, Texas a & M Health Science Center, Dallas, Texas, 75246.
Taha AzimaieDepartment of Biomedical Sciences, Baylor College of Dentistry, Texas a & M Health Science Center, Dallas, Texas, 75246.
Megan F VeltenMaterial Science and Engineering Department, University of Texas at Arlington, Arlington, Texas, 76019.
Michael VuDepartment of Biomedical Sciences, Baylor College of Dentistry, Texas a & M Health Science Center, Dallas, Texas, 75246.
Mark B LylesVADM Joel T, Boone Chair of Health and Security Studies, U.S. Naval War College, Center for Naval Warfare Studies, Newport, Rhode Island, 02841.
Harry K KimCenter for Excellence in Hip Disorders, Texas Scottish Rite Hospital for Children, Dallas, Texas, 75219.
Pranesh B AswathMaterial Science and Engineering Department, University of Texas at Arlington, Arlington, Texas, 76019.
Venu G VaranasiDepartment of Biomedical Sciences, Baylor College of Dentistry, Texas a & M Health Science Center, Dallas, Texas, 75246.
The University of Texas at Arlington · USNaval War College · USTexas Scottish Rite Hospital for Children · US

Funding

Silicon, a Novel Antioxidant Role in Bone HealingR03DE023872 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI VARANASI, VENU GOPAL · 2014 to 2015
$229k
NIDCR NIH HHS R03 DE023872NIDCR NIH HHS R03DE023872-01
6 · The paper itself

Abstract

Current synthetic grafts for bone defect filling in the sinus can support new bone formation but lack the ability to stimulate or enhance osteogenic healing. To promote such healing, osteoblast progenitors such as human periosteum cells must undergo osteogenic differentiation. In this study, we tested the hypothesis that degradation of porous amorphous silica fibrous (PASF) scaffolds can enhance human periosteum cell osteogenic differentiation. Two types of PASF were prepared and evaluated according to their densities (PASF99, PASF98) with 99 and 98% porosity, respectively. Silicon (Si) ions were observed to rapidly release from both scaffolds within 24 h in vitro. PASF99 Si ion release rate was estimated to be nearly double that of PASF98 scaffolds. Mechanical tests revealed a lower compressive strength in PASF99 as compared with PASF98. Osteogenic expression analysis showed that PASF99 scaffolds enhanced the expression of activating transcription factor 4, alkaline phosphatase, and collagen (Col(I)α1, Col(I)α2). Scanning electron microscopy showed cellular and extracellular matrix (ECM) ingress into both scaffolds within 16 days and the formation of Ca-P precipitates within 85 days. In conclusion, this study demonstrated that PASF scaffolds enhance human periosteum cell osteogenic differentiation by releasing ionic Si, and structurally supporting cellular and ECM ingress.

Indexed as

SiliconTissue ScaffoldsCell DifferentiationCells, CulturedHumansPeriosteumSiliconosteocalcinperiosteum cellRunx2scaffoldSi

Identifiers

PMID25630903
PMCPMC6556392
OpenAlexW2119017100

What OpenQuestion holds

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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.