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Suppression of Osteoarthritis progression by post-natal Induction of Nkx3.2.
Oh, Hye-Kyoung; Park, Minsun; Choi, Seung-Won; Jeong, Da-Un; Kim, Byoung Ju; Kim, Jeong-Ah; Choi, Hye-Jeong; Lee, Jimin; Cho, Yongsik; Kim, Jin-Hong; Seong, Je Kyung; Choi, Byung Hyune; Min, Byoung-Hyun; Kim, Dae-Won.
Afiliação
  • Oh HK; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
  • Park M; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
  • Choi SW; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
  • Jeong DU; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
  • Kim BJ; Department of Medical Biotechnology, Dongguk University-Seoul, Seoul, Republic of Korea.
  • Kim JA; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
  • Choi HJ; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
  • Lee J; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
  • Cho Y; Department of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, Republic of Korea.
  • Kim JH; Department of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, Republic of Korea.
  • Seong JK; Korea Mouse Phenotyping Center, Seoul National University, Seoul, Republic of Korea.
  • Choi BH; Department of Biomedical Sciences, Inha University College of Medicine, Incheon, Republic of Korea.
  • Min BH; Department of Orthopedic Surgery, Ajou University School of Medicine, Suwon, Republic of Korea; Department of Molecular Science and Technology, Ajou University, Suwon, Republic of Korea.
  • Kim DW; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea. Electronic address: kimdw@yonsei.ac.kr.
Biochem Biophys Res Commun ; 571: 188-194, 2021 09 24.
Article em En | MEDLINE | ID: mdl-34330063
ABSTRACT
Osteoarthritis (OA) is an incurable joint disease affecting 240 million elderly population, and major unmet medical needs exist for better therapeutic options for OA. During skeletal development, Nkx3.2 has been shown to promote chondrocyte differentiation and survival, but to suppress cartilage hypertrophy and blood vessel invasion. Here we show that Nkx3.2 plays a key role in osteoarthritis (OA) pathogenesis. Marked reduction of Nkx3.2 expression was observed in three different murine OA models. Consistent with these findings, analyses of surgery-induced and age-driven OA models revealed that cartilage-specific post-natal induction of Nkx3.2 can suppress OA progression in mice. These results suggest that Nkx3.2 may serve as a promising target for OA drug development.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoartrite / Fatores de Transcrição / Proteínas de Homeodomínio Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoartrite / Fatores de Transcrição / Proteínas de Homeodomínio Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2021 Tipo de documento: Article