Evidence map›Paper›PMID 27787811›Full record

ArticleJournal of materials science. Materials in medicine2016

Cell-protection mechanism through autophagy in HGFs/S. mitis co-culture treated with Chitlac-nAg.

Marialucia Gallorini, Viviana di Giacomo, Valentina Di Valerio, Monica Rapino, Domenico Bosco, Andrea Travan, Mara Di Giulio, Roberta Di Pietro, Sergio Paoletti, Amelia Cataldi and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of materials science. Materials in medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. A Current Overview of the Biological and Cellular Effects of Nanosilver.International journal of molecular sciences · 2018
    Review
  5. 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

11 authors at 3 institutions in 2 countries.

Marialucia GalloriniDepartment of Pharmacy, "G. d'Annunzio" University, Chieti-Pescara, Italy.
Viviana di GiacomoDepartment of Pharmacy, "G. d'Annunzio" University, Chieti-Pescara, Italy. v.digiacomo@unich.it.
Valentina Di ValerioDepartment of Medicine and Ageing Sciences, "G. d'Annunzio" University, Chieti-Pescara, Italy.
Monica RapinoGenetic Molecular Institute of CNR, Unit of Chieti, "G. d'Annunzio" University, Chieti-Pescara, Italy.
Domenico BoscoGenetic Molecular Institute of CNR, Unit of Chieti, "G. d'Annunzio" University, Chieti-Pescara, Italy.
Andrea TravanDepartment of Life Sciences, University of Trieste, Trieste, Italy.
Mara Di GiulioDepartment of Pharmacy, "G. d'Annunzio" University, Chieti-Pescara, Italy.
Roberta Di PietroDepartment of Medicine and Ageing Sciences, "G. d'Annunzio" University, Chieti-Pescara, Italy.
Sergio PaolettiDepartment of Life Sciences, University of Trieste, Trieste, Italy.
Amelia CataldiDepartment of Pharmacy, "G. d'Annunzio" University, Chieti-Pescara, Italy.
Silvia SancilioDepartment of Pharmacy, "G. d'Annunzio" University, Chieti-Pescara, Italy.
University of Chieti-Pescara · ITUniversity of Trieste · ITUniversity Hospital Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Silver-based products have been proven to be effective in retarding and preventing bacterial growth since ancient times. In the field of restorative dentistry, the use of silver ions/nanoparticles has been explored to counteract bacterial infections, as silver can destroy bacterial cell walls by reacting with membrane proteins. However, it is also cytotoxic towards eukaryotic cells, which are capable of internalizing nanoparticles. In this work, we investigated the biological effects of Chitlac-nAg, a colloidal system based on a modified chitosan (Chitlac), administered for 24-48 h to a co-culture of primary human gingival fibroblasts and Streptococcus mitis in the presence of saliva, developed to mimic the microenvironment of the oral cavity. We sought to determine its efficiency to combat oral hygiene-related diseases without affecting eukaryotic cells. Cytotoxicity, reactive oxygen species production, apoptosis induction, nanoparticles uptake, and lysosome and autophagosome metabolism were evaluated. In vitro results show that Chitlac-nAg does not exert cytotoxic effects on human gingival fibroblasts, which seem to survive through a homoeostasis mechanism involving autophagy. That suggests that the novel biomaterial Chitlac-nAg could be a promising tool in the field of dentistry.

Indexed as

AutophagyCoculture TechniquesBacterial AdhesionCell SurvivalChitosanColloidsDental MaterialsFibroblastsFlow CytometryGingivaHumansIonsL-Lactate DehydrogenaseMetal NanoparticlesMicroscopy, Electron, TransmissionReactive Oxygen SpeciesChitosanColloidsDental MaterialsIonsL-Lactate DehydrogenaseReactive Oxygen SpeciesSilver

Identifiers

PMID27787811
OpenAlexW2545855752

What OpenQuestion holds

Textmetadata
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.