Detalhes do Documento

Role of NOD2 and RIP2 in host-microbe interactions with Gram-negative bacteria: Insights from the periodontal disease model

Autor(es): Souza, Joao A.C. [UNESP] ; Medeiros, Marcell C. [UNESP] ; Rocha, Fernanda R.G. [UNESP] ; De Aquino, Sabrina G. [UNESP] ; Ávila-Campos, Mario J. ; Spolidorio, Luis C. [UNESP] ; Zamboni, Dario S. ; Graves, Dana T. ; Rossa, Carlos [UNESP]

Data: 2018

Identificador Persistente: http://hdl.handle.net/11449/173651

Origem: Oasisbr

Assunto(s): Bone resorption; inflammation; innate immunity; macrophages; NOD2 signaling adaptor protein


Descrição

Made available in DSpace on 2018-12-11T17:07:05Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-11-01

National Institute of Dental and Craniofacial Research

NOD2 is a member of the NLR family of proteins that participate in the activation of the innate immune response. RIP2 is a downstream kinase activated by both NOD1 and NOD2. There is scarcity of information regarding the relevance of NOD2 in periodontitis, a chronic inflammatory condition characterized by inflammatory bone resorption. We used NOD2-KO and RIP2-KO mice in a model of microbial-induced periodontitis. Heat-killed Aggregatibacter actinomycetemcomitans was injected in the gingival tissues three times/wk for 4 wk. Bone resorption was assessed by μCT analysis; osteoclasts were identified by immunohistochemical staining for TRAP and inflammation was assessed using a severity score system in H/E-stained sections. In vitro studies using primary macrophages assessed the response macrophages using qPCR-based array and multi-ligand ELISA. Bone resorption and osteoclastogenesis were significantly reduced in NOD2-KO mice. Severity of inflammation was not affected. qPCR-focused arrays and multi-ligand ELISA showed that expression of pro-inflammatory mediators was reduced in NOD2- and RIP2-deficient cells. RANKL-induced osteoclastogenesis was impaired in NOD2- and RIP2-deficient macrophages. We conclude that NOD2 is important for osteoclast differentiation and inflammatory bone resorption in vivo and also for the macrophage response to Gram-negative bacteria.

Department of Diagnosis and Surgery School of Dentistry at Araraquara Univ Estadual Paulista (UNESP), Rua Humaita, 1680, Centro

Department of Microbiology Institute of Biomedical Sciences-Univ de Sao Paulo (USP)

Department of Physiology and Pathology School of Dentistry at Araraquara-Univ Estadual Paulista (UNESP)

Department of Cell Molecular Biology and Biopathogenic Agents School of Medicine at Ribeirao Preto-Univ de Sao Paulo (USP)

Department of Periodontics School of Dental Medicine-University of Pennsylvania

Department of Diagnosis and Surgery School of Dentistry at Araraquara Univ Estadual Paulista (UNESP), Rua Humaita, 1680, Centro

Department of Physiology and Pathology School of Dentistry at Araraquara-Univ Estadual Paulista (UNESP)

National Institute of Dental and Craniofacial Research: R01DE017732

National Institute of Dental and Craniofacial Research: R01DE021921

Tipo de Documento Artigo científico
Idioma Inglês
facebook logo  linkedin logo  twitter logo 
mendeley logo

Documentos Relacionados

Não existem documentos relacionados.