Department of Neurology, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, PR China.
Department of Oncology, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, PR China.
Exp Cell Res. 2022 Aug 1;417(1):113132. doi: 10.1016/j.yexcr.2022.113132. Epub 2022 Apr 6.
Parkinson's disease (PD) is a common neurodegenerative disease. Here, the purpose of the study was to explore the function of long non-coding RNA (lncRNA) HOX transcript antisense RNA (HOTAIR) in PD and its underlying mechanism. An in vivo 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-hydrochloride (MPTP)-induced mouse model of PD was generated and the SH-SY5Y cells were treated with MPP to induce neuronal damage in vitro. Quantitative real-time polymerase chain reaction (QRT-PCR) and Western blot were used to detect the expression of HOTAIR, miR-221-3p, α-synuclein and apoptosis-related genes. MTT, flow cytometry and TUNEL assay was used to detect cell viability and apoptosis, respectively. The levels of inflammatory cytokines TNF-α,IL-1β and IL-6 were detected by ELISA assay. The levels of lactate dehydrogenase (LDH), reactive oxygen species (ROS), and superoxide dismutase (SOD) were determined using the appropriate assay kits. The interactions between miR-221-3p and HOTAIR or α-synuclein were determined by dual luciferase assay and RNA binding protein immunoprecipitation (RIP). Co-localization of HOTAIR and miR-221-3p was also proved by immunofluorescence staining. The results showed that HOTAIR was highly expressed, while miR-221-3p expression was decreased in PD model in vivo and in vitro. In SH-SY5Y cells treated with MPP, the knockdown of HOTAIR increased cell viability and reduced cell apoptosis, the secretion of inflammatory cytokines and oxidative stress reaction, while HOTAIR overexpression led to opposite effects. Furthermore, HOTAIR sponged miR-221-3p which directly targeted α-synuclein and thus regulated the expression of α-synuclein. Meanwhile, inhibiting miR-221-3p could partially reverse the neuroprotective effects of HOTAIR knockdown. In conclusion, HOTAIR attenuated the injury of SH-SY5Y cells induced by MPP via miR-221-3p/α-synuclein axis, suggesting the potential therapeutic value of HOTAIR in PD.
帕金森病(PD)是一种常见的神经退行性疾病。本研究旨在探讨长链非编码 RNA(lncRNA)HOX 转录反义 RNA(HOTAIR)在 PD 中的作用及其潜在机制。建立了体内 1-甲基-4-苯基-1,2,3,6-四氢吡啶盐酸盐(MPTP)诱导的 PD 小鼠模型,并在体外使用 MPP 处理 SH-SY5Y 细胞诱导神经元损伤。采用实时定量聚合酶链反应(QRT-PCR)和 Western blot 检测 HOTAIR、miR-221-3p、α-突触核蛋白和凋亡相关基因的表达。MTT、流式细胞术和 TUNEL 检测分别用于检测细胞活力和凋亡。酶联免疫吸附试验(ELISA)检测炎症细胞因子 TNF-α、IL-1β 和 IL-6 的水平。采用相应的试剂盒测定乳酸脱氢酶(LDH)、活性氧(ROS)和超氧化物歧化酶(SOD)的水平。双荧光素酶报告基因和 RNA 结合蛋白免疫沉淀(RIP)实验检测 miR-221-3p 与 HOTAIR 或 α-突触核蛋白的相互作用。免疫荧光染色也证明了 HOTAIR 和 miR-221-3p 的共定位。结果显示,在体内和体外 PD 模型中,HOTAIR 表达升高,而 miR-221-3p 表达降低。在 MPP 处理的 SH-SY5Y 细胞中,HOTAIR 敲低可增加细胞活力并减少细胞凋亡,降低炎症细胞因子和氧化应激反应的分泌,而过表达 HOTAIR 则产生相反的效果。此外,HOTAIR 可吸附 miR-221-3p,而 miR-221-3p 可直接靶向α-突触核蛋白,从而调节α-突触核蛋白的表达。同时,抑制 miR-221-3p 可部分逆转 HOTAIR 敲低的神经保护作用。综上所述,HOTAIR 通过 miR-221-3p/α-突触核蛋白轴减轻 MPP 诱导的 SH-SY5Y 细胞损伤,提示 HOTAIR 在 PD 中的潜在治疗价值。