AT1 and AT2 Receptor Knockout Changed Osteonectin and Bone Density in Mice in Periodontal Inflammation Experimental Model

Background: The aim of this study was to evaluate the role of AT1 and AT2 receptors in a periodontal inflammation experimental model. Methods: Periodontal inflammation was induced by LPS/<i>Porphyromonas gingivalis</i>. Maxillae, femur, and vertebra were scanned using Micro-CT. Maxillae...

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Main Authors: Maria Laura de Souza Lima, Caroline Addison Carvalho Xavier de Medeiros, Gerlane Coelho Bernardo Guerra, Robson Santos, Michael Bader, Flavia Q. Pirih, Raimundo Fernandes de Araújo Júnior, Alan B. Chan, Luis J. Cruz, Gerly Anne de Castro Brito, Renata Ferreira de Carvalho Leitão, Ericka Janine Dantas da Silveira, Vinicius Barreto Garcia, Agnes Andrade Martins, Aurigena Antunes de Araújo
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/10/5217
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author Maria Laura de Souza Lima
Caroline Addison Carvalho Xavier de Medeiros
Gerlane Coelho Bernardo Guerra
Robson Santos
Michael Bader
Flavia Q. Pirih
Raimundo Fernandes de Araújo Júnior
Alan B. Chan
Luis J. Cruz
Gerly Anne de Castro Brito
Renata Ferreira de Carvalho Leitão
Ericka Janine Dantas da Silveira
Vinicius Barreto Garcia
Agnes Andrade Martins
Aurigena Antunes de Araújo
spellingShingle Maria Laura de Souza Lima
Caroline Addison Carvalho Xavier de Medeiros
Gerlane Coelho Bernardo Guerra
Robson Santos
Michael Bader
Flavia Q. Pirih
Raimundo Fernandes de Araújo Júnior
Alan B. Chan
Luis J. Cruz
Gerly Anne de Castro Brito
Renata Ferreira de Carvalho Leitão
Ericka Janine Dantas da Silveira
Vinicius Barreto Garcia
Agnes Andrade Martins
Aurigena Antunes de Araújo
AT1 and AT2 Receptor Knockout Changed Osteonectin and Bone Density in Mice in Periodontal Inflammation Experimental Model
International Journal of Molecular Sciences
bone
micro-computed tomography
periodontitis
inflammation
osteonectin
author_facet Maria Laura de Souza Lima
Caroline Addison Carvalho Xavier de Medeiros
Gerlane Coelho Bernardo Guerra
Robson Santos
Michael Bader
Flavia Q. Pirih
Raimundo Fernandes de Araújo Júnior
Alan B. Chan
Luis J. Cruz
Gerly Anne de Castro Brito
Renata Ferreira de Carvalho Leitão
Ericka Janine Dantas da Silveira
Vinicius Barreto Garcia
Agnes Andrade Martins
Aurigena Antunes de Araújo
author_sort Maria Laura de Souza Lima
title AT1 and AT2 Receptor Knockout Changed Osteonectin and Bone Density in Mice in Periodontal Inflammation Experimental Model
title_short AT1 and AT2 Receptor Knockout Changed Osteonectin and Bone Density in Mice in Periodontal Inflammation Experimental Model
title_full AT1 and AT2 Receptor Knockout Changed Osteonectin and Bone Density in Mice in Periodontal Inflammation Experimental Model
title_fullStr AT1 and AT2 Receptor Knockout Changed Osteonectin and Bone Density in Mice in Periodontal Inflammation Experimental Model
title_full_unstemmed AT1 and AT2 Receptor Knockout Changed Osteonectin and Bone Density in Mice in Periodontal Inflammation Experimental Model
title_sort at1 and at2 receptor knockout changed osteonectin and bone density in mice in periodontal inflammation experimental model
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-05-01
description Background: The aim of this study was to evaluate the role of AT1 and AT2 receptors in a periodontal inflammation experimental model. Methods: Periodontal inflammation was induced by LPS/<i>Porphyromonas gingivalis</i>. Maxillae, femur, and vertebra were scanned using Micro-CT. Maxillae were analyzed histopathologically, immunohistochemically, and by RT-PCR. Results: The vertebra showed decreased BMD in AT1 H compared with WT H (<i>p</i> < 0.05). The femur showed increased Tb.Sp for AT1 H and AT2 H, <i>p</i> < 0.01 and <i>p</i> < 0.05, respectively. The Tb.N was decreased in the vertebra (WT H-AT1 H: <i>p</i> < 0.05; WT H-AT2 H: <i>p</i> < 0.05) and in the femur (WT H-AT1 H: <i>p</i> < 0.01; WT H-AT2 H: <i>p</i> < 0.05). AT1 PD increased linear bone loss (<i>p</i> < 0.05) and decreased osteoblast cells (<i>p</i> < 0.05). RANKL immunostaining was intense for AT1 PD and WT PD (<i>p</i> < 0.001). OPG was intense in the WT H, WT PD, and AT2 PD when compared to AT1 PD (<i>p</i> < 0.001). AT1 PD showed weak immunostaining for osteocalcin compared with WT H, WT PD, and AT2 PD (<i>p</i> < 0.001). AT1 H showed significantly stronger immunostaining for osteonectin in fibroblasts compared to AT2 H (<i>p</i> < 0.01). Conclusion: AT1 receptor knockout changed bone density, the quality and number of bone trabeculae, decreased the number of osteoblast cells, and increased osteonectin in fibroblasts.
topic bone
micro-computed tomography
periodontitis
inflammation
osteonectin
url https://www.mdpi.com/1422-0067/22/10/5217
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spelling doaj-e964afffadf54bd48b5fa7d987fff2332021-06-01T00:04:32ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-05-01225217521710.3390/ijms22105217AT1 and AT2 Receptor Knockout Changed Osteonectin and Bone Density in Mice in Periodontal Inflammation Experimental ModelMaria Laura de Souza Lima0Caroline Addison Carvalho Xavier de Medeiros1Gerlane Coelho Bernardo Guerra2Robson Santos3Michael Bader4Flavia Q. Pirih5Raimundo Fernandes de Araújo Júnior6Alan B. Chan7Luis J. Cruz8Gerly Anne de Castro Brito9Renata Ferreira de Carvalho Leitão10Ericka Janine Dantas da Silveira11Vinicius Barreto Garcia12Agnes Andrade Martins13Aurigena Antunes de Araújo14Postgraduate Program in Dentistry Sciences, Department of Biophysical and Pharmacology, Federal University of Rio Grande Norte, Natal, RN 59078-900, BrazilPostgraduate Program in Biological Science, Postgraduate Program in RENORBIO, Department of Biophysical and Pharmacology, Federal University of Rio Grande Norte, Natal, RN 59078-970, BrazilPostgraduate Program in Biological Science, Postgraduate Program in Pharmaceutical Science, Department of Biophysical and Pharmacology, Federal University of Rio Grande Norte, Natal, RN 59078-970, BrazilDepartment of Physiology, Federal University of Minas Gerais, Belo Horizonte, MG 31270-901, BrazilMax Delbrück Center of Molecular Medicine, 13125 Berlin, GermanySchool of Dentistry, Universidad California-Los Angeles (UCLA), Los Angeles, CA 90095, USAPost Graduate Program Functional and Structural Biology, Post Graduate Program Health Science, Department of Morphology, Federal University of Rio Grande do Norte, 3000 Senador Salgado Filho Ave, Lagoa Nova, Natal, RN 59078-970, BrazilPercuros B.V, 2333 CL Leiden, The NetherlandsTranslational Nanobiomaterials and Imaging, Department of Radiology, Leiden University Medical Center, 2333 ZA Leiden, The NetherlandsPostgraduate Program in Pharmacology, Postgraduate Program in Morphology, Department of Morphology, Fortaleza, CE 60430-170, BrazilPostgraduate Program in Morphology, Department of Morphology, Fortaleza, CE 60430-170, BrazilPostgraduate Program in Dentistry Sciences, Department of Biophysical and Pharmacology, Federal University of Rio Grande Norte, Natal, RN 59078-900, BrazilPostgraduate Program in Health Sciences, Cancer and Inflammation Research laboratory, Department of Morphology, Federal University of Rio Grande Norte, Natal, RN 59078-970, BrazilDepartment of Dentistry, Federal University of Rio Grande Norte, Natal, RN 59078-970, BrazilPostgraduate Program in Dentistry Sciences, Department of Biophysical and Pharmacology, Federal University of Rio Grande Norte, Natal, RN 59078-900, BrazilBackground: The aim of this study was to evaluate the role of AT1 and AT2 receptors in a periodontal inflammation experimental model. Methods: Periodontal inflammation was induced by LPS/<i>Porphyromonas gingivalis</i>. Maxillae, femur, and vertebra were scanned using Micro-CT. Maxillae were analyzed histopathologically, immunohistochemically, and by RT-PCR. Results: The vertebra showed decreased BMD in AT1 H compared with WT H (<i>p</i> < 0.05). The femur showed increased Tb.Sp for AT1 H and AT2 H, <i>p</i> < 0.01 and <i>p</i> < 0.05, respectively. The Tb.N was decreased in the vertebra (WT H-AT1 H: <i>p</i> < 0.05; WT H-AT2 H: <i>p</i> < 0.05) and in the femur (WT H-AT1 H: <i>p</i> < 0.01; WT H-AT2 H: <i>p</i> < 0.05). AT1 PD increased linear bone loss (<i>p</i> < 0.05) and decreased osteoblast cells (<i>p</i> < 0.05). RANKL immunostaining was intense for AT1 PD and WT PD (<i>p</i> < 0.001). OPG was intense in the WT H, WT PD, and AT2 PD when compared to AT1 PD (<i>p</i> < 0.001). AT1 PD showed weak immunostaining for osteocalcin compared with WT H, WT PD, and AT2 PD (<i>p</i> < 0.001). AT1 H showed significantly stronger immunostaining for osteonectin in fibroblasts compared to AT2 H (<i>p</i> < 0.01). Conclusion: AT1 receptor knockout changed bone density, the quality and number of bone trabeculae, decreased the number of osteoblast cells, and increased osteonectin in fibroblasts.https://www.mdpi.com/1422-0067/22/10/5217bonemicro-computed tomographyperiodontitisinflammationosteonectin