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Collagen-Induced Arthritis Analysis in Rhbdf2 Knockout Mouse
Biomolecules & Therapeutics ; : 298-305, 2018.
Artigo em Inglês | WPRIM | ID: wpr-714736
ABSTRACT
Rhomboid family member 2 gene (Rhbdf2) is an inactive homologue lacking essential catalytic residues of rhomboid intramembrane serine proteases. The protein is necessary for maturation of tumor necrosis factor-alpha (TNF-α) converting enzyme, which is the molecule responsible for the release of TNF-α. In this study, Rhbdf2 knockout (KO) mice were produced by CRISPR/CAS9. To see the effects of the failure of TNF-α release induced by Rhbdf2 gene KO, collagen-induced arthritis (CIA), which is the representative TNF-α related disease, was induced in the Rhbdf2 mutant mouse using chicken collagen type II. The severity of the CIA was measured by traditional clinical scores and histopathological analysis of hind limb joints. A rota-rod test and grip strength test were employed to evaluate the severity of CIA based on losses of physical functions. The results indicated that Rhbdf2 mutant mice showed clear alleviation of the clinical severity of CIA as demonstrated by the significantly lower severity indexes. Moreover, a grip strength test was shown to be useful for the evaluation of physical functional losses by CIA. Overall, the results showed that the Rhbdf2 gene has a significant effect on the induction of CIA, which is related to TNF-α.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Artrite Experimental / Galinhas / Fator de Necrose Tumoral alfa / Camundongos Knockout / Força da Mão / Colágeno Tipo II / Extremidades / Serina Proteases / Articulações Limite: Animais / Humanos Idioma: Inglês Revista: Biomolecules & Therapeutics Ano de publicação: 2018 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Artrite Experimental / Galinhas / Fator de Necrose Tumoral alfa / Camundongos Knockout / Força da Mão / Colágeno Tipo II / Extremidades / Serina Proteases / Articulações Limite: Animais / Humanos Idioma: Inglês Revista: Biomolecules & Therapeutics Ano de publicação: 2018 Tipo de documento: Artigo