Department of Orthopedic Surgery, Washington University School of Medicine, St Louis, United States.
Department of Mechanical Engineering and Material Sciences, Washington University School of Medicine, St Louis, United States.
Elife. 2022 Aug 2;11:e80725. doi: 10.7554/eLife.80725.
Osteoarthritis is the most common joint disease in the world with significant societal consequences but lacks effective disease-modifying interventions. The pathophysiology consists of a prominent inflammatory component that can be targeted to prevent cartilage degradation and structural defects. Intracellular metabolism has emerged as a culprit of the inflammatory response in chondrocytes, with both processes co-regulating each other. The role of glutamine metabolism in chondrocytes, especially in the context of inflammation, lacks a thorough understanding and is the focus of this work. We display that mouse chondrocytes utilize glutamine for energy production and anabolic processes. Furthermore, we show that glutamine deprivation itself causes metabolic reprogramming and decreases the inflammatory response of chondrocytes through inhibition of NF-κB activity. Finally, we display that glutamine deprivation promotes autophagy and that ammonia is an inhibitor of autophagy. Overall, we identify a relationship between glutamine metabolism and inflammatory signaling and display the need for increased study of chondrocyte metabolic systems.
骨关节炎是世界上最常见的关节疾病,对社会有重大影响,但缺乏有效的疾病修正干预措施。其病理生理学主要为炎症反应,该反应可针对其进行靶向治疗,以防止软骨降解和结构缺陷。细胞内代谢已成为软骨细胞炎症反应的罪魁祸首,这两个过程相互调节。谷氨酰胺代谢在软骨细胞中的作用,特别是在炎症的背景下,仍缺乏全面的了解,这是这项工作的重点。我们发现,小鼠软骨细胞利用谷氨酰胺进行能量生成和合成代谢。此外,我们还表明,谷氨酰胺剥夺本身会导致代谢重编程,并通过抑制 NF-κB 活性降低软骨细胞的炎症反应。最后,我们发现谷氨酰胺剥夺可促进自噬,而氨是自噬的抑制剂。总的来说,我们确定了谷氨酰胺代谢与炎症信号之间的关系,并显示需要增加对软骨细胞代谢系统的研究。