Response to oxidative stress of peripheral blood mononuclear cells from multiple sclerosis patients and healthy controls

被引:0
作者
Cristiana Pistono
Maria Cristina Monti
Chiara Boiocchi
Francesca Gigli Berzolari
Cecilia Osera
Giulia Mallucci
Mariaclara Cuccia
Alessia Pascale
Cristina Montomoli
Roberto Bergamaschi
机构
[1] University of Pavia,Laboratory of Immunogenetics, Department of Biology and Biotechnology “L. Spallanzani”
[2] CNRS/Université de Strasbourg,Laboratoire de Neurosciences Cognitives et Adaptatives (LNCA)
[3] Faculté de psychologie,Department of Public Health Experimental and Forensic Medicine, Unit of Biostatistics and Clinical Epidemiology
[4] University of Pavia,Inter
[5] National Neurological Institute “C. Mondino”,Department Multiple Sclerosis Research Centre
[6] University of Pavia,Department of Drug Sciences, Section of Pharmacology
来源
Cell Stress and Chaperones | 2020年 / 25卷
关键词
Multiple sclerosis; HSP70-2; rs1061581; Oxidative stress; PBMCs; Hydrogen peroxide;
D O I
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中图分类号
学科分类号
摘要
The complex scenario of multiple sclerosis (MS) pathology involves several mechanisms, including oxidative stress response. The heat shock proteins (HSPs) are important for the protection of the cells; however, their role in MS is not clear. The present research is focused on the response of peripheral blood mononuclear cells (PBMCs) to oxidative stress and to the involvement of HSP70-2 (a protein coded by the HSPA1B gene, located in the MHC class III). To this aim, we challenged PBMCs from MS patients and healthy controls with hydrogen peroxide. Specifically, PBMCs mitochondrial activity, HSP70-2 protein expression and the production of intracellular reactive oxygen species were assessed. These parameters were also related to the HSP70-2 rs1061581 polymorphism, which is linked to the risk of developing MS. Moreover, mitochondrial activity and HSP70-2 protein levels were also related to disease severity. Overall, our results indicate that PBMCs, from both MS patients and healthy controls, may display a similar response towards an oxidative insult; within this context, HSP70-2 does not seem to be central in the protection of PBMCs. Nevertheless, the HSP70-2 rs1061581 polymorphism is related to ROS levels and appears to have a role in the different expression of HSP70-2 under oxidative stimulus.
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页码:81 / 91
页数:10
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