LincR-PPP2R5C Promotes Th2 Cell Differentiation Through PPP2R5C/ PP2A by Forming an RNA-DNA Triplex in Allergic Asthma

被引:5
作者
Ji, Ningfei [1 ]
Chen, Zhongqi [1 ]
Wang, Zhengxia [1 ]
Sun, Wei [2 ]
Yuan, Qi [1 ]
Zhang, Xijie [1 ]
Jia, Xinyu [1 ]
Wu, Jingjing [1 ]
Jiang, Jingxian [1 ]
Song, Meijuan [1 ]
Xu, Tingting [1 ]
Liu, Yanan [1 ]
Ma, Qiyun [1 ]
Sun, Zhixiao [1 ]
Bao, Yanmin [3 ]
Zhang, Mingshun [4 ,5 ]
Huang, Mao [1 ,6 ]
机构
[1] Nanjing Med Univ, Dept Resp & Crit Care Med, Affiliated Hosp 1, Nanjing, Peoples R China
[2] Southeast Univ, Xishan Peoples Hosp Wuxi City, Dept Resp & Crit Care Med, Wuxi Branch,Zhongda Hosp, Wuxi, Peoples R China
[3] Shenzhen Childrens Hosp, Dept Resp Med, Shenzhen, Peoples R China
[4] Nanjing Med Univ, Jiangsu Prov Engn Res Ctr Antibody Drugs, Dept Immunol, NHC Key Lab Antibody Tech, Nanjing, Peoples R China
[5] Nanjing Med Univ, Jiangsu Prov Engn Res Ctr Antibody Drugs, Dept Immunol, NHC Key Lab Antibody Tech, 140 Hanzhong Rd, Nanjing 210029, Peoples R China
[6] Nanjing Med Univ, Affiliated Hosp 1, Dept Resp & Crit Care Med, 300 Guangzhou Rd, Nanjing 210029, Peoples R China
基金
中国国家自然科学基金;
关键词
LncRNA; Th2; cells; asthma; protein phosphatase 2; inflammation; LONG NONCODING RNAS; MOUSE MODELS; PHOSPHATASES; EXPRESSION; GENOMICS;
D O I
10.4168/aair.2024.16.1.71
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Purpose: The roles and mechanisms of long noncoding RNAs (lncRNAs) in T helper 2 (Th2) differentiation from allergic asthma are poorly understood. We aimed to explore a novel lncRNA, LincR-protein phosphatase 2 regulatory subunit B' gamma (PPP2R5C), in Th2 differentiation in a mouse model of asthma. Methods: LincR-PPP2R5C from RNA-seq data of CD4+ T cells of asthma-like mice were validated and confirmed by quantitative reverse transcription polymerase chain reaction, northern blotting, nuclear and cytoplasmic separation, and fluorescence in situ hybridization (FISH). Lentiviruses encoding LincR-PPP2R5C or shRNA were used to overexpress or silence LincR-PPP2R5C in CD4+ T cells. The interactions between LincR-PPP2R5C and PPP2R5C were explored with western blotting, chromatin isolation by RNA purification assay, and fluorescence resonance energy transfer. An ovalbumin-induced acute asthma model in knockout (1(O) mice (LincR-PPP2R5C 1(O, CD4 conditional LincR-PPP2R5C 1(O) was established to explore the roles of LincR-PPP2R5C in Th2 differentiation. Results: LncR-PPP2R5C was significantly higher in CD4+ T cells from asthmatic mice ex vivo and Th2 cells in vitro. The lentivirus encoding LincR-PPP2R5C suppressed Th1 differentiation; in contrast, the short hairpin RNA (shRNA) lentivirus decreased LincR-PPP2R5C and Th2 differentiation. Mechanistically, LincR-PPP2R5C deficiency suppressed the phosphatase activity of the protein phosphatase 2A (PP2A) holocomplex, resulting in a decline in Th2 differentiation. The formation of an RNA-DNA triplex between LincR-PPP2R5C and the PPP2R5C promoter enhanced PPP2R5C expression and activated PP2A. LincR-PPP2R5C 1(O and CD4 conditional 1(O decreased Th2 differentiation, airway hyperresponsiveness and inflammatory responses. Conclusions: LincR-PPP2R5C regulated PPP2R5C expression and PP2A activity by forming an RNA-DNA triplex with the PPP2R5C promoter, leading to Th2 polarization in a mouse model of acute asthma. Our data presented the first definitive evidence of lncRNAs in the regulation of Th2 cells in asthma.
引用
收藏
页码:71 / 90
页数:20
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