Evidence map›Paper›PMID 26018305›Full record

ArticleJournal of applied oral science : revista FOB

Exposure of periodontal ligament progenitor cells to lipopolysaccharide from Escherichia coli changes osteoblast differentiation pattern.

Mayra Laino Albiero, Bruna Rabelo Amorim, Luciane Martins, Márcio Zaffalon Casati, Enilson Antonio Sallum, Francisco Humberto Nociti, Karina Gonzales Silvério

Open access · diamondAbstract read
In one paragraph

Article in Journal of applied oral science : revista FOB. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

20 citing papers in PubMed, 42 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

7 authors at 1 institution in 1 country.

Mayra Laino AlbieroDivision of Periodontics, Piracicaba Dental School, State University of Campinas, Piracicaba, SP, Brazil.
Bruna Rabelo AmorimDivision of Periodontics, Piracicaba Dental School, State University of Campinas, Piracicaba, SP, Brazil.
Luciane MartinsDivision of Periodontics, Piracicaba Dental School, State University of Campinas, Piracicaba, SP, Brazil.
Márcio Zaffalon CasatiDivision of Periodontics, Piracicaba Dental School, State University of Campinas, Piracicaba, SP, Brazil.
Enilson Antonio SallumDivision of Periodontics, Piracicaba Dental School, State University of Campinas, Piracicaba, SP, Brazil.
Francisco Humberto NocitiDivision of Periodontics, Piracicaba Dental School, State University of Campinas, Piracicaba, SP, Brazil.
Karina Gonzales SilvérioDivision of Periodontics, Piracicaba Dental School, State University of Campinas, Piracicaba, SP, Brazil.
Universidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledPeriodontal ligament mesenchymal stem cells (PDLMSCs) are an important alternative source of adult stem cells and may be applied for periodontal tissue regeneration, neuroregenerative medicine, and heart valve tissue engineering. However, little is known about the impact of bacterial toxins on the biological properties of PDLSMSCs, including self-renewal, differentiation, and synthesis of extracellular matrix.

objectiveThis study investigated whether proliferation, expression of pro-inflammatory cytokines, and osteogenic differentiation of CD105-enriched PDL progenitor cell populations (PDL-CD105(+) cells) would be affected by exposure to bacterial lipopolysaccharide from Escherichia coli (EcLPS). MATERIAL AND

methodsToll-like receptor 4 (TLR4) expression was assessed in PDL-CD105(+) cells by the immunostaining technique and confirmed using Western blotting assay. Afterwards, these cells were exposed to EcLPS, and the following assays were carried out: (i) cell viability using MTS; (ii) expression of the interleukin-1 beta (IL-1β), interleukin-6 (IL-6), interleukin-8 (IL-8), and tumor necrosis factor alpha (TNF-α) genes; (iii) osteoblast differentiation assessed by mineralization in vitro, and by mRNA levels of run-related transcription factor-2 (RUNX2), alkaline phosphatase (ALP) and osteocalcin (OCN) determined by quantitative PCR.

resultsPDL-CD105+ cells were identified as positive for TLR4. EcLPS did not affect cell viability, but induced a significant increase of transcripts for IL-6 and IL-8. Under osteogenic condition, PDL-CD105+ cells exposed to EcLPS presented an increase of mineralized matrix deposition and higher RUNX2 and ALP mRNA levels when compared to the control group.

conclusionsThese results provide evidence that CD105-enriched PDL progenitor cells are able to adapt to continuous Escherichia coli endotoxin challenge, leading to an upregulation of osteogenic activities.

Indexed as

Antigens, CDBlotting, WesternCell DifferentiationCells, CulturedCell SurvivalCytokinesEndoglinEscherichia coliHumansLipopolysaccharidesMesenchymal Stem CellsOsteoblastsOsteogenesisPeriodontal LigamentPolymerase Chain ReactionReceptors, Cell SurfaceAntigens, CDCytokinesEndoglinENG protein, humanLipopolysaccharidesReceptors, Cell SurfaceToll-Like Receptor 4

Identifiers

PMID26018305
PMCPMC4428458
OpenAlexW2227228198

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.