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巨噬细胞迁移抑制因子在神经退行性变中的双重作用

The Dichotomic Role of Macrophage Migration Inhibitory Factor in Neurodegeneration.

作者信息

Basile Maria Sofia, Battaglia Giuseppe, Bruno Valeria, Mangano Katia, Fagone Paolo, Petralia Maria Cristina, Nicoletti Ferdinando, Cavalli Eugenio

机构信息

Department of Biomedical and Biotechnological Sciences, University of Catania, Via S. Sofia 89, 95123 Catania, Italy.

Department of Physiology and Pharmacology, Sapienza University, Piazzale A. Moro, 5, 00185 Rome, Italy.

出版信息

Int J Mol Sci. 2020 Apr 24;21(8):3023. doi: 10.3390/ijms21083023.

Abstract

Macrophage migration inhibitory factor (MIF) is a pleiotropic cytokine expressed by different cell types and exerting multiple biological functions. It has been shown that MIF may be involved in several disorders, including neurodegenerative disorders such as amyotrophic lateral sclerosis (ALS), Parkinson disease (PD), and Huntington disease (HD), that represent an unmet medical need. Therefore, further studies are needed to identify novel pathogenetic mechanisms that may translate into tailored therapeutic approaches so to improve patients' survival and quality of life. Here, we reviewed the preclinical and clinical studies investigating the role of MIF in ALS, PD, and HD. The emerging results suggest that MIF might play a dichotomic role in these disorders, exerting a protective action in ALS, a pathogenetic action in HD, and a yet undefined and debated role in PD. The better understanding of the role of MIF in these diseases could allow its use as a novel diagnostic and therapeutic tool for the monitoring and treatment of the patients and for eventual biomarker-driven therapeutic approaches.

摘要

巨噬细胞移动抑制因子(MIF)是一种由不同细胞类型表达并发挥多种生物学功能的多效性细胞因子。已有研究表明,MIF可能参与多种疾病,包括肌萎缩侧索硬化症(ALS)、帕金森病(PD)和亨廷顿病(HD)等神经退行性疾病,这些疾病目前仍存在未满足的医疗需求。因此,需要进一步研究以确定可能转化为针对性治疗方法的新发病机制,从而提高患者的生存率和生活质量。在此,我们综述了研究MIF在ALS、PD和HD中作用的临床前和临床研究。新出现的结果表明,MIF在这些疾病中可能发挥双重作用,在ALS中发挥保护作用,在HD中发挥致病作用,而在PD中的作用尚不清楚且存在争议。更好地理解MIF在这些疾病中的作用可能使其作为一种新型诊断和治疗工具用于监测和治疗患者以及最终基于生物标志物的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8ec/7216212/127b01018a32/ijms-21-03023-g001.jpg

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