Author
Listed:
- Young-Ok Son
(Gwangju Institute of Science and Technology)
- Seulki Park
(Gwangju Institute of Science and Technology)
- Ji-Sun Kwak
(Gwangju Institute of Science and Technology)
- Yoonkyung Won
(Gwangju Institute of Science and Technology)
- Wan-Su Choi
(Gwangju Institute of Science and Technology)
- Jinseol Rhee
(Gwangju Institute of Science and Technology)
- Churl-Hong Chun
(Wonkwang University School of Medicine)
- Je-Hwang Ryu
(School of Dentistry, Chonnam National University)
- Don-Kyu Kim
(Chonnam National University)
- Hueng-Sik Choi
(Chonnam National University)
- Jang-Soo Chun
(Gwangju Institute of Science and Technology)
Abstract
The estrogen-related receptor (ERR) family of orphan nuclear receptor is composed of ERRα, ERRβ, and ERRγ, which are known to regulate various isoform-specific functions under normal and pathophysiological conditions. Here, we investigate the involvement of ERRs in the pathogenesis of osteoarthritis (OA) in mice. Among ERR family members, ERRγ is markedly upregulated in cartilage from human OA patients and various mouse models of OA. Adenovirus-mediated overexpression of ERRγ in mouse knee joint or transgenic expression of ERRγ in cartilage leads to OA. ERRγ overexpression in chondrocytes directly upregulates matrix metalloproteinase (MMP)-3 and MMP13, which are known to play crucial roles in cartilage destruction in OA. In contrast, genetic ablation of Esrrg or shRNA-mediated downregulation of Esrrg in joint tissues abrogates experimental OA in mice. Our results collectively indicate that ERRγ is a novel catabolic regulator of OA pathogenesis.
Suggested Citation
Young-Ok Son & Seulki Park & Ji-Sun Kwak & Yoonkyung Won & Wan-Su Choi & Jinseol Rhee & Churl-Hong Chun & Je-Hwang Ryu & Don-Kyu Kim & Hueng-Sik Choi & Jang-Soo Chun, 2017.
"Estrogen-related receptor γ causes osteoarthritis by upregulating extracellular matrix-degrading enzymes,"
Nature Communications, Nature, vol. 8(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-01868-8
DOI: 10.1038/s41467-017-01868-8
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