Estrogen antagonizes ASIC1a-induced chondrocyte mitochondrial stress in rheumatoid arthritis

• Published in: Journal of translational medicine Vol. 20; no. 1; pp. 561 - 14
• Main Authors: Zai, Zhuoyan, Xu, Yayun, Qian, Xuewen, Li, Zihan, Ou, Ziyao, Zhang, Tao, Wang, Longfei, Ling, Yian, Peng, Xiaoqing, Zhang, Yihao, Chen, Feihu
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 03-12-2022; BioMed Central; BMC
• Subjects: Acid Sensing Ion Channels - genetics; Acid Sensing Ion Channels - metabolism; Acidification; Acidosis; Acids; Animals; Apoptosis; Arthritis, Experimental; Arthritis, Rheumatoid - genetics; Arthritis, Rheumatoid - metabolism; ASIC1a; Calcium (mitochondrial); Calcium influx; Cartilage; Cartilage (articular); Cartilage, Articular - drug effects; Cartilage, Articular - pathology; Cell culture; Chondrocytes; Chondrocytes - drug effects; Chondrocytes - metabolism; Confocal microscopy; Cytoplasm; Diagnosis; Disease; Egtazic Acid - metabolism; Egtazic Acid - toxicity; Estrogen; Estrogens; Estrogens - pharmacology; Ethylene glycol; Gene expression; Genetic aspects; Health aspects; Immunofluorescence; Inflammation; Membrane potential; Membranes; Mitochondria; Mitochondria - drug effects; Mitochondria - metabolism; Mitochondrial Proteins - genetics; Mitochondrial Proteins - metabolism; Mitochondrial stress; Ovariectomy; Rats; Reactive Oxygen Species; Rheumatoid arthritis; Transmission electron microscopy; China; United States > US; Germany; Mitochondrial stress; ASIC1a; Rheumatoid arthritis; Calcium influx; Estrogen
• ISSN: 1479-5876; 1479-5876
• DOI: 10.1186/s12967-022-03781-1

Destruction of articular cartilage and bone is the main cause of joint dysfunction in rheumatoid arthritis (RA). Acid-sensing ion channel 1a (ASIC1a) is a key molecule that mediates the destruction of RA articular cartilage. Estrogen has been proven to have a protective effect against articular cartilage damage, however, the underlying mechanisms remain unclear.
We treated rat articular chondrocytes with an acidic environment, analyzed the expression levels of mitochondrial stress protein HSP10, ClpP, LONP1 by q-PCR and immunofluorescence staining. Transmission electron microscopy was used to analyze the mitochondrial morphological changes. Laser confocal microscopy was used to analyze the Ca
, mitochondrial membrane potential (Δψm) and reactive oxygen species (ROS) level. Moreover, ASIC1a specific inhibitor Psalmotoxin 1 (Pctx-1) and Ethylene Glycol Tetraacetic Acid (EGTA) were used to observe whether acid stimulation damage mitochondrial function through Ca
influx mediated by ASIC1a and whether pretreatment with estrogen could counteract these phenomena. Furthermore, the ovariectomized (OVX) adjuvant arthritis (AA) rat model was treated with estrogen to explore the effect of estrogen on disease progression.
Our results indicated that HSP10, ClpP, LONP1 protein and mRNA expression and mitochondrial ROS level were elevated in acid-stimulated chondrocytes. Moreover, acid stimulation decreased mitochondrial membrane potential and damaged mitochondrial structure of chondrocytes. Furthermore, ASIC1a specific inhibitor PcTx-1 and EGTA inhibited acid-induced mitochondrial abnormalities. In addition, estrogen could protect acid-stimulated induced mitochondrial stress by regulating the activity of ASIC1a in rat chondrocytes and protects cartilage damage in OVX AA rat.
Extracellular acidification induces mitochondrial stress by activating ASIC1a, leading to the damage of rat articular chondrocytes. Estrogen antagonizes acidosis-induced joint damage by inhibiting ASIC1a activity. Our study provides new insights into the protective effect and mechanism of action of estrogen in RA.