The role of selenium metabolism and selenoproteins in cartilage homeostasis and arthropathies

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作者
Donghyun Kang
Jeeyeon Lee
Cuiyan Wu
Xiong Guo
Byeong Jae Lee
Jang-Soo Chun
Jin-Hong Kim
机构
[1] Center for RNA Research,Department of Biological Sciences, College of Natural Sciences
[2] Institute for Basic Science,School of Public Health
[3] Seoul National University,Interdisciplinary Program in Bioinformatics
[4] Xi’an Jiaotong University,National Creative Research Initiatives Center for Osteoarthritis Pathogenesis and School of Life Sciences
[5] Seoul National University,undefined
[6] Gwangju Institute of Science and Technology,undefined
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摘要
As an essential nutrient and trace element, selenium is required for living organisms and its beneficial roles in human health have been well recognized. The role of selenium is mainly played through selenoproteins synthesized by the selenium metabolic system. Selenoproteins have a wide range of cellular functions including regulation of selenium transport, thyroid hormones, immunity, and redox homeostasis. Selenium deficiency contributes to various diseases, such as cardiovascular disease, cancer, liver disease, and arthropathy—Kashin–Beck disease (KBD) and osteoarthritis (OA). A skeletal developmental disorder, KBD has been reported in low-selenium areas of China, North Korea, and the Siberian region of Russia, and can be alleviated by selenium supplementation. OA, the most common form of arthritis, is a degenerative disease caused by an imbalance in matrix metabolism and is characterized by cartilage destruction. Oxidative stress serves as a major cause of the initiation of OA pathogenesis. Selenium deficiency and dysregulation of selenoproteins are associated with impairments to redox homeostasis in cartilage. We review the recently explored roles of selenium metabolism and selenoproteins in cartilage with an emphasis on two arthropathies, KBD and OA. Moreover, we discuss the potential of therapeutic strategies targeting the biological functions of selenium and selenoproteins for OA treatment.
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页码:1198 / 1208
页数:10
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