Altahla Ruba, Tao Xu
Department of Rehabilitation, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Metabolites. 2024 Sep 7;14(9):488. doi: 10.3390/metabo14090488.
Thioredoxin-interacting protein (TXNIP) has been involved in oxidative stress and activation of the NOD-like receptor protein-3 (NLRP3) inflammasome, directly linking it to the pyroptosis pathway. Furthermore, pyroptosis may contribute to the inflammatory process in osteoarthritis (OA). The purpose of this study was to investigate the role of TXNIP in activating the NLRP3 inflammasome through the pyroptosis pathway in an OA rat model. Destabilization of the medial meniscus (DMM) was induced in the OA model with intra-articular injections of adeno-associated virus (AAV) overexpressing (OE) or knocking down (KD) TXNIP. A total of 48 healthy rats were randomly divided into six groups (N = 8 each). During the experiment, the rats' weights, mechanical pain thresholds, and thermal pain thresholds were measured weekly. Morphology staining, micro-CT, 3D imaging, and immunofluorescence (IF) staining were used to measure the expression level of TXNIP, and ELISA techniques were employed. OE-TXNIP-AAV in DMM rats aggravated cartilage destruction and subchondral bone loss, whereas KD-TXNIP slowed the progression of OA. The histological results showed that DMM modeling and OE-TXNIP-AAV intra-articular injection caused joint structure destruction, decreased anabolic protein expression, and increased catabolic protein expression and pyroptosis markers. Conversely, KD-TXNIP-AAV slowed joint degeneration. OE-TXNIP-AVV worsened OA by accelerating joint degeneration and damage, while KD-TXNIP-AAV treatment had a protective effect.
硫氧还蛋白相互作用蛋白(TXNIP)参与了氧化应激和NOD样受体蛋白3(NLRP3)炎性小体的激活,直接将其与细胞焦亡途径联系起来。此外,细胞焦亡可能促成骨关节炎(OA)的炎症过程。本研究的目的是在OA大鼠模型中探究TXNIP通过细胞焦亡途径激活NLRP3炎性小体的作用。通过关节腔内注射过表达(OE)或敲低(KD)TXNIP的腺相关病毒(AAV),在OA模型中诱导内侧半月板失稳(DMM)。总共48只健康大鼠被随机分为六组(每组N = 8)。在实验过程中,每周测量大鼠的体重、机械痛阈和热痛阈。采用形态学染色、显微CT、三维成像和免疫荧光(IF)染色来检测TXNIP的表达水平,并运用酶联免疫吸附测定(ELISA)技术。DMM大鼠体内的OE-TXNIP-AAV加剧了软骨破坏和软骨下骨丢失,而KD-TXNIP减缓了OA的进展。组织学结果显示,DMM建模和关节腔内注射OE-TXNIP-AAV导致关节结构破坏、合成代谢蛋白表达降低、分解代谢蛋白表达增加以及细胞焦亡标志物增多。相反,KD-TXNIP-AAV减缓了关节退变。OE-TXNIP-AVV通过加速关节退变和损伤使OA恶化,而KD-TXNIP-AAV治疗具有保护作用。