The Role of Ferroptosis in the Pathogenesis of Osteoarthritis

被引:21
|
作者
Al-Hetty, Hussein Riyadh Abdul Kareem [1 ]
Abdulameer, Sada Jasim [2 ]
Alghazali, Maha Waleed [3 ]
Sheri, Fatime Satar [4 ]
Saleh, Marwan Mahmood [5 ,6 ]
Jalil, Abduladheem Turki [7 ]
机构
[1] Al Maarif Univ Coll, Dept Nursing, Ramadi, Iraq
[2] Wasit Univ, Coll Educ Pure Sci, Dept Biol, Kut, Iraq
[3] Al Rafidain Univ Coll, Dept Dent, Baghdad, Iraq
[4] Natl Univ Sci & Technol, Coll Dent, Dhi Qar, Iraq
[5] Univ Anbar, Coll Appl Sci, Dept Biophys, Ramadi, Iraq
[6] Islamic Univ, Coll Med Technol, Dept Med Lab Technol, Najaf, Iraq
[7] Al Mustaqbal Univ Coll, Dept Med Labs Tech, Babylon, Iraq
来源
JOURNAL OF MEMBRANE BIOLOGY | 2023年 / 256卷 / 03期
关键词
Ferroptosis; GPX4; Iron; Lipid peroxides; Osteoarthritis; DENDROSOMAL CURCUMIN NANOFORMULATION; APOPTOSIS; EXPRESSION; NECROSIS; FORM;
D O I
10.1007/s00232-023-00282-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Osteoarthritis (OA) is the most common type of arthritis. Its high prevalence, especially in the elderly, and its negative impact on physical function make it a leading cause of disability in the elderly. Joint pain as well joint stiffness are the common classic signs of OA. Chondrocyte death together with loss of articular cartilage integrity are the main pathologic changes in OA. Non-steroidal anti-inflammatory drugs (NSAIDs) and glucocorticoids are commonly used for the management of OA; still, their effectiveness is limited, and no therapeutic strategy is able to fully stop OA progression. Ferroptosis is a kind of cell death, distinct from apoptosis and necroptosis, caused by iron-dependent peroxidation of membrane phospholipids that terminates cell life by disintegrating all plasma membranes. It has been suggested that ferroptosis has a critical role in decreased viability of chondrocytes in OA, and here, we review recent findings regarding the pathologic pathways that lead to chondrocyte ferroptosis, and discuss the possible therapeutic utility of ferroptosis inhibition in OA.
引用
收藏
页码:223 / 228
页数:6
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