CircSSR1 regulates pyroptosis of pulmonary artery smooth muscle cells through parental protein SSR1 mediating endoplasmic reticulum stress

• Published in: Respiratory research Vol. 25; no. 1; pp. 355 - 16
• Main Authors: Guan, Xiaoyu, Du, Hongxia, Wang, Xiaoying, Zhu, Xiangrui, Ma, Cui, Zhang, Lixin, He, Siyu, Bai, June, Liu, Huiyu, Yuan, Hao, Wang, Shanshan, Wan, Kuiyu, Yu, Hang, Zhu, Daling
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 01.10.2024; BioMed Central; BMC
• Subjects: Analysis; Animals; Apoptosis; Care and treatment; Cells, Cultured; CircRNA; Complications and side effects; Endoplasmic reticulum stress; Endoplasmic Reticulum Stress - physiology; Gene expression; Health aspects; Hypertension, Pulmonary - genetics; Hypertension, Pulmonary - metabolism; Hypertension, Pulmonary - pathology; m6A; Male; Medical examination; Membrane Proteins; Mice; Mice, Inbred C57BL; Muscle, Smooth, Vascular - metabolism; Muscle, Smooth, Vascular - pathology; Myocytes, Smooth Muscle - metabolism; Myocytes, Smooth Muscle - pathology; Pulmonary Artery - metabolism; Pulmonary Artery - pathology; Pulmonary hypertension; Pyroptosis; Pyroptosis - physiology; RNA, Circular - genetics; RNA, Circular - metabolism; Smooth muscle; Stress (Physiology); China; m6A; Pyroptosis; CircRNA; Pulmonary hypertension; Endoplasmic reticulum stress
• DOI: 10.1186/s12931-024-02986-w
• ISSN: 1465-993X; 1465-9921

Pyroptosis, inflammatory necrosis of cells, is a programmed cell death involved in the pathological process of diseases. Endoplasmic reticulum stress (ERS), as a protective stress response of cell, decreases the unfold protein concentration to inhibit the unfold protein agglutination. Whereas the relationship between endoplasmic reticulum stress and pyroptosis in pulmonary hypertension (PH) remain unknown. Previous evident indicated that circular RNA (circRNA) can participate in several biological process, including cell pyroptosis. However, the mechanism of circRNA regulate pyroptosis of pulmonary artery smooth muscle cells through endoplasmic reticulum stress still unclear. Here, we proved that circSSR1 was down-regulate expression during hypoxia in pulmonary artery smooth muscle cells, and over-expression of circSSR1 inhibit pyroptosis both in vitro and in vivo under hypoxic. Our experiments have indicated that circSSR1 could promote host gene SSR1 translation via m6A to activate ERS leading to pulmonary artery smooth muscle cell pyroptosis. In addition, our results showed that G3BP1 as upstream regulator mediate the expression of circSSR1 under hypoxia. These results highlight a new regulatory mechanism for pyroptosis and provide a potential therapy target for pulmonary hypertension. RNA-FISH and qRT-PCR were showed the location of circSSR1 and expression change. RNA pull-down and RIP verify the circSSR1 combine with YTHDF1. Western blotting, PI staining and LDH release were used to explore the role of circSSR1 in PASMCs pyroptosis. CircSSR1 was markedly downregulated in hypoxic PASMCs. Knockdown CircSSR1 inhibited hypoxia induced PASMCs pyroptosis in vivo and in vitro. Mechanistically, circSSR1 combine with YTHDF1 to promote SSR1 protein translation rely on m6A, activating pyroptosis via endoplasmic reticulum stress. Furthermore, G3BP1 induce circSSR1 degradation under hypoxic. Our findings clarify the role of circSSR1 up-regulated parental protein SSR1 expression mediate endoplasmic reticulum stress leading to pyroptosis in PASMCs, ultimately promoting the development of pulmonary hypertension.