LncRNA NEAT1, an Important Biomarker Involved in the Pathological and Physiological Processes of Parkinson's Disease.

Runsen Chen, Yuxi Zhang, Yang Shen, Kede Wu, Xuming Mo, Zhaocong Yang
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Abstract

Parkinson's disease (PD) is a complex progressive neurodegenerative disorder and the pathogenesis and treatment methods are unknown. This aim is to investigate the effects of long non coding RNA NEAT1 (LncRNA NEAT1) on 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced Parkinson's disease (PD). Immunoprecipitation and western blot were used to search for the effects of LncRNA NEAT1 on PD. Tyrosine hydroxylase (TH) and brain derived neurotrophic factor (BDNF) were evaluated in substantia nigra (SN) region of the brain by immunohistochemical staining. Compared with the control group, the relative expression level of LncRNA NEAT1 in the MPTP group was significantly increased. LncRNA NEAT1 is negatively correlated with miR-376b-3p. LncRNA NEAT1 significantly increased oxidative stress, neuroinflammation along with enhanced neurotrophic potential via NLR family Pyrin domain protein 3 (NLRP3) pathway. In conclusion, these results indicated that LncRNA NEAT1 participated in the pathophysiological of PD and its mechanism via the miR-376b-3p/NLRP3 signaling pathway.

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参与帕金森病病理和生理过程的重要生物标志物LncRNA NEAT1
帕金森病(PD)是一种复杂的进行性神经退行性疾病,其发病机制和治疗方法尚不清楚。目的是研究长链非编码RNA NEAT1 (LncRNA NEAT1)在1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的帕金森病(PD)中的作用。免疫沉淀和western blot检测LncRNA NEAT1对PD的影响。采用免疫组化染色法检测大鼠脑黑质区酪氨酸羟化酶(TH)和脑源性神经营养因子(BDNF)水平。与对照组相比,MPTP组LncRNA NEAT1的相对表达量显著升高。LncRNA NEAT1与miR-376b-3p呈负相关。LncRNA NEAT1通过NLR家族Pyrin结构域蛋白3 (NLRP3)通路显著增加氧化应激、神经炎症和神经营养电位。综上所述,这些结果表明LncRNA NEAT1通过miR-376b-3p/NLRP3信号通路参与PD的病理生理及其机制。
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Modulation of Intestinal Inflammation and Protection of Dopaminergic Neurons in Parkinson's Disease Mice through a Probiotic Formulation Targeting NLRP3 Inflammasome. The High-Affinity IL-2 Receptor Affects White Matter Damage after Cerebral Ischemia by Regulating CD8 + T Lymphocyte Differentiation. LncRNA NEAT1, an Important Biomarker Involved in the Pathological and Physiological Processes of Parkinson's Disease. Ghrelin Induces Ferroptosis Resistance and M2 Polarization of Microglia to Alleviate Neuroinflammation and Cognitive Impairment in Alzheimer's Disease. Empagliflozin Mitigates PTZ-Induced Seizures in Rats: Modulating Npas4 and CREB-BDNF Signaling Pathway.
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