Inhibition of Leukotriene A4 Hydrolase Suppressed Cartilage Degradation and Synovial Inflammation in a Mouse Model of Experimental Osteoarthritis.

IF 2.7 4区 医学 Q1 ORTHOPEDICS
CARTILAGE Pub Date : 2024-06-01 Epub Date: 2023-04-21 DOI:10.1177/19476035231169940
Xiaoxin Wu, Antonia RuJia Sun, Ross Crawford, Yin Xiao, Yanping Wang, Indira Prasadam, Xinzhan Mao
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引用次数: 0

Abstract

Objective: Chronic inflammation plays an important role in the osteoarthritis (OA) pathology but how this influence OA disease progression is unclear. Leukotriene B4 (LTB4) is a potent proinflammatory lipid mediator generated from arachidonic acid through the sequential activities of 5-lipoxygenase, 5-lipoxygenase-activating protein, Leukotriene A4 hydrolase (LTA4H) and its downstream product LTB4. The aim of this study is to investigate the involvement and the potential therapeutic target of the LTB4 pathway in OA disease progression.

Design: Both clinical human cartilage samples (n = 7) and mice experimental OA models (n = 6) were used. The levels of LTA4H and leukotriene B4 receptor 1 were first examined using immunostaining in human OA/non-OA cartilage and mice experimental OA models. We also determined whether the LTA4H pathway was associated with cartilage degeneration and synovitis inflammation in OA mice models and human articular chondrocytes.

Results: We found that both LTA4H and LTB4 receptor (BLT1) were highly expressed in human and mice OA cartilage. Inhibition of LTA4H suppressed cartilage degeneration and synovitis in OA mice model. Furthermore, inhibition of LTA4H promoted cartilage regeneration by upregulating chondrogenic genes expression such as aggrecan (ACAN), collagen 2A1 (COL2A1), and SRY-Box transcription factor 9 (SOX9).

Conclusions: Our results indicate that the LTA4H pathway is a crucial regulator of OA pathogenesis and suggest that LTA4H could be a therapeutic target in combat OA.

抑制白三烯 A4水解酶可抑制实验性骨关节炎小鼠模型的软骨退化和滑膜炎症。
目的:慢性炎症在骨关节炎(OA)病理学中扮演着重要角色,但其如何影响 OA 疾病的进展尚不清楚。白三烯 B4(LTB4)是一种由花生四烯酸通过 5-脂氧合酶、5-脂氧合酶激活蛋白、白三烯 A4 水解酶(LTA4H)及其下游产物 LTB4 的连续活动生成的强效促炎脂质介质。本研究旨在探讨LTB4通路在OA疾病进展中的参与情况及其潜在治疗靶点:设计:采用临床人类软骨样本(n = 7)和小鼠实验性 OA 模型(n = 6)。设计:采用临床人类软骨样本(n = 7)和小鼠实验性 OA 模型(n = 6),首先用免疫染色法检测人类 OA/非 OA 软骨和小鼠实验性 OA 模型中 LTA4H 和白三烯 B4 受体 1 的水平。我们还确定了 LTA4H 通路是否与 OA 小鼠模型和人类关节软骨细胞的软骨退化和滑膜炎症有关:结果:我们发现LTA4H和LTB4受体(BLT1)在人和小鼠OA软骨中均高表达。抑制 LTA4H 可抑制 OA 小鼠模型的软骨退化和滑膜炎。此外,抑制LTA4H可通过上调软骨生成基因(如凝集素(ACAN)、胶原蛋白2A1(COL2A1)和SRY-Box转录因子9(SOX9))的表达促进软骨再生:我们的研究结果表明,LTA4H通路是OA发病机制的关键调节因子,并提示LTA4H可作为抗击OA的治疗靶点。
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来源期刊
CARTILAGE
CARTILAGE ORTHOPEDICS-
CiteScore
6.90
自引率
7.10%
发文量
80
期刊介绍: CARTILAGE publishes articles related to the musculoskeletal system with particular attention to cartilage repair, development, function, degeneration, transplantation, and rehabilitation. The journal is a forum for the exchange of ideas for the many types of researchers and clinicians involved in cartilage biology and repair. A primary objective of CARTILAGE is to foster the cross-fertilization of the findings between clinical and basic sciences throughout the various disciplines involved in cartilage repair. The journal publishes full length original manuscripts on all types of cartilage including articular, nasal, auricular, tracheal/bronchial, and intervertebral disc fibrocartilage. Manuscripts on clinical and laboratory research are welcome. Review articles, editorials, and letters are also encouraged. The ICRS envisages CARTILAGE as a forum for the exchange of knowledge among clinicians, scientists, patients, and researchers. The International Cartilage Repair Society (ICRS) is dedicated to promotion, encouragement, and distribution of fundamental and applied research of cartilage in order to permit a better knowledge of function and dysfunction of articular cartilage and its repair.
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