Evidence map›Paper›PMID 29066255›Full record

ArticleImmunobiology2018

Comparative analysis of microbial sensing molecules in mucosal tissues with aging.

O A Gonzalez, S Kirakodu, M J Novak, A J Stromberg, L Orraca, J Gonzalez-Martinez, A Burgos, J L Ebersole

Abstract readComparative Study
In one paragraph

Article in Immunobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

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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.

O A GonzalezCenter for Oral Health Research, College of Dentistry, University of Kentucky, Lexington, KY, United States.
S KirakoduCenter for Oral Health Research, College of Dentistry, University of Kentucky, Lexington, KY, United States.
M J NovakCenter for Oral Health Research, College of Dentistry, University of Kentucky, Lexington, KY, United States.
A J StrombergSchool of Dental Medicine, University of Puerto Rico, San Juan, PR, United States.
L OrracaDepartment of Statistics, College of Arts and Sciences, University of Kentucky, Lexington, KY, United States.
J Gonzalez-MartinezCaribbean Primate Research Center, University of Puerto Rico, Toa Baja, PR, United States.
A BurgosCaribbean Primate Research Center, University of Puerto Rico, Toa Baja, PR, United States.
J L EbersoleCenter for Oral Health Research, College of Dentistry, University of Kentucky, Lexington, KY, United States. Electronic address: jleber2@uky.edu.

Funding

WKU Lead Faculty AwardP20GM103436 · NIGMS · UNIVERSITY OF LOUISVILLE · PI ERIC C ROUCHKA · 2012 to 2026
$60.1M
Translational Science InitiativeP40OD012217 · OD · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI CARLOS A SARIOL · 2012 to 2026
$40.4M
Translational Research at the CPRC:genetic model of primate circadian disorderP40RR003640 · NCRR · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI KRAISELBURD, EDMUNDO NELSON · 1987 to 2011
$21.1M
UKY DENTAL COBRE: POLYBACTERIAL PERIODONTITIS: N-3 PUFA AND ANTIOXIDANTSP20RR020145 · NCRR · UNIVERSITY OF KENTUCKY · PI NOVAK, MICHAEL JOHN · 2004 to 2011
$18.3M
Kentucky Center for Clinical and Translational ScienceUL1TR000117 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$13.3M
OHPP Oral Health Pilot Program P30GM110788 · NIGMS · UNIVERSITY OF KENTUCKY · PI EBERSOLE, JEFFREY L · 2014 to 2018
$5.4M
Center for the Biologic Basis of Oral/Systemic Disease (CBBOSD)P20GM103538 · NIGMS · UNIVERSITY OF KENTUCKY · PI EBERSOLE, JEFFREY L · 2012 to 2013
$4.2M
NCATS NIH HHS UL1 TR000117NCRR NIH HHS P20 RR020145NCRR NIH HHS P40 RR003640NIGMS NIH HHS P20 GM103436NIGMS NIH HHS P20 GM103538NIGMS NIH HHS P30 GM110788NIH HHS P40 OD012217
6 · The paper itself

Abstract

Host-bacterial interactions at mucosal surfaces require recognition of the bacteria by host cells enabling targeted responses to maintain tissue homeostasis. It is now well recognized that an array of host-derived pattern recognition receptors (PRRs), both cell-bound and soluble, are critical to innate immune engagement of microbes via microbial-associated molecular patterns (MAMP). This report describes the use of a nonhuman primate model to evaluate changes in the expression of these sensing molecules related to aging in healthy gingival tissues. Macaca mulatta aged 3-24 years were evaluated clinically and gingival tissues obtained, RNA isolated and microarray analysis conducted for gene expression of the sensing pattern recognition receptors (PRRs). The results demonstrated increased expression of various PRRs in healthy aging gingiva including extracellular (CD14, CD209, CLEC4E, TLR4), intracellular (NAIP, IFIH1, DAI) and soluble (PTX4, SAA1) PRRs. Selected PRRs were also correlated with both bleeding on probing (BOP) and pocket depth (PD) in the animals. These findings suggest that aged animals express altered levels of various PRRs that could affect the ability of the tissues to interact effectively with the juxtaposed microbial ecology, presumably contributing to an enhanced risk of periodontitis even in clinically healthy oral mucosal tissues with aging.

Indexed as

AgingAnimalsGingivaGingivitisHomeostasisHost-Pathogen InteractionsHumansMacaca mulattaMicroarray AnalysisModels, AnimalMouth MucosaPathogen-Associated Molecular Pattern MoleculesPeriodontitisReceptors, Pattern RecognitionTranscriptomePathogen-Associated Molecular Pattern MoleculesReceptors, Pattern RecognitionAgingMicrobial sensingNonhuman primatesOral mucosaPattern recognition receptorsPeriodontitis

Identifiers

PMID29066255
PMCPMC5821569

What OpenQuestion holds

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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.