Estrogen deficiency during puberty affects the expression of microRNA30a and microRNA503 in the mandibular condyle.


Journal

Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft
ISSN: 1618-0402
Titre abrégé: Ann Anat
Pays: Germany
ID NLM: 100963897

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 13 07 2021
revised: 18 10 2021
accepted: 11 11 2021
pubmed: 24 11 2021
medline: 4 2 2022
entrez: 23 11 2021
Statut: ppublish

Résumé

The aim of this study was investigated if estrogen deficiency during puberty affects the expression of miRNA30a and miRNA503 in maxillary and mandibular growth centers, and also evaluated if ERα and ERβ are correlated with miRNA30a and miRNA503 expressions. Samples from 12 female Wistar rats randomized into experimental group (OVX) and control group (SHAM). At an age of 45 days animals were euthanized for miRNA expression analyses. RT-qPCR was performed to determine miRNA30a and miRNA503 expression in growth sites: midpalatal suture, condyle, mandibular angle, symphysis/parasymphysis and coronoid process. The data was carried out using the parametric tests at 5% of significance level. miRNA 30a and miRNA503 presented higher levels in the condylar site in SHAM group when compared with OVX (p = 0.002 and p = 0.020, respectively). In the growth centers, a statistical significant difference was observed only for miRNA30a (p = 0.004), when compared mandibular angle with condyle the in OVX group (p = 0.001). A strong positive correlation between miRNA503 and ERα in the condyle of OVX group was observed (r = 0.90; p = 0.039 and it also between miRNA503 and ERβ in the coronoid process of the OVX group (r = 0.88; p = 0.05). The results suggested that estrogen regulates specific miRNAs in maxillary and mandibular growth centers, which may participate in posttranscriptional regulation of estrogen-regulated genes.

Sections du résumé

BACKGROUND BACKGROUND
The aim of this study was investigated if estrogen deficiency during puberty affects the expression of miRNA30a and miRNA503 in maxillary and mandibular growth centers, and also evaluated if ERα and ERβ are correlated with miRNA30a and miRNA503 expressions.
METHODS METHODS
Samples from 12 female Wistar rats randomized into experimental group (OVX) and control group (SHAM). At an age of 45 days animals were euthanized for miRNA expression analyses. RT-qPCR was performed to determine miRNA30a and miRNA503 expression in growth sites: midpalatal suture, condyle, mandibular angle, symphysis/parasymphysis and coronoid process. The data was carried out using the parametric tests at 5% of significance level.
RESULTS RESULTS
miRNA 30a and miRNA503 presented higher levels in the condylar site in SHAM group when compared with OVX (p = 0.002 and p = 0.020, respectively). In the growth centers, a statistical significant difference was observed only for miRNA30a (p = 0.004), when compared mandibular angle with condyle the in OVX group (p = 0.001). A strong positive correlation between miRNA503 and ERα in the condyle of OVX group was observed (r = 0.90; p = 0.039 and it also between miRNA503 and ERβ in the coronoid process of the OVX group (r = 0.88; p = 0.05).
CONCLUSION CONCLUSIONS
The results suggested that estrogen regulates specific miRNAs in maxillary and mandibular growth centers, which may participate in posttranscriptional regulation of estrogen-regulated genes.

Identifiants

pubmed: 34813926
pii: S0940-9602(21)00191-6
doi: 10.1016/j.aanat.2021.151865
pii:
doi:

Substances chimiques

Estrogen Receptor alpha 0
Estrogen Receptor beta 0
Estrogens 0
MIRN503 microRNA, human 0
MicroRNAs 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

151865

Informations de copyright

Copyright © 2021. Published by Elsevier GmbH.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Ana Zilda Nazar Bergamo (AZN)

Department of Pediatric Clinic, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.

Isabela Ribeiro Madalena (IR)

Department of Pediatric Clinic, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil; Department of Dentistry, University of the Region of Joinville, Joinville, SC, Brazil; Department of Restorative Dentistry, Federal University of Juiz de Fora, Juiz de Fora, MG, Brazil.

Marjorie Ayumi Omori (MA)

Department of Pediatric Clinic, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.

Lucas Alexandre Ramazzotto (LA)

Department of Pediatric Clinic, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil; Biotechnology Graduation, Federal University of São Carlos, São Carlos, SP, Brazil.

Paulo Nelson-Filho (P)

Department of Pediatric Clinic, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.

Flares Baratto-Filho (F)

Department of Dentistry, University of the Region of Joinville, Joinville, SC, Brazil.

Peter Proff (P)

Department of Orthodontics, University Medical Centre of Regensburg, Germany.

Christian Kirschneck (C)

Department of Orthodontics, University Medical Centre of Regensburg, Germany. Electronic address: christian.kirschneck@klinik.uni-regensburg.de.

Erika Calvano Küchler (EC)

Department of Orthodontics, University Medical Centre of Regensburg, Germany. Electronic address: erikacalvano@gmail.com.

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Classifications MeSH