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

Cell Stress and Chaperones Pub Date : 2020-01-01 Epub Date: 2019-11-12 DOI:10.1007/s12192-019-01049-0
Cristiana Pistono, Maria Cristina Monti, Chiara Boiocchi, Francesca Gigli Berzolari, Cecilia Osera, Giulia Mallucci, Mariaclara Cuccia, Alessia Pascale, Cristina Montomoli, Roberto Bergamaschi
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Abstract

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.

多发性硬化症患者和健康对照组外周血单核细胞对氧化应激的反应。
多发性硬化症(MS)病理过程复杂,涉及多种机制,包括氧化应激反应。热休克蛋白(HSPs)对保护细胞非常重要,但它们在多发性硬化症中的作用尚不明确。本研究的重点是外周血单核细胞(PBMC)对氧化应激的反应以及 HSP70-2(一种由 HSPA1B 基因编码的蛋白质,位于 MHC III 类)的参与。为此,我们用过氧化氢挑战了多发性硬化症患者和健康对照组的 PBMCs。具体来说,我们评估了 PBMC 的线粒体活性、HSP70-2 蛋白表达和细胞内活性氧的产生。这些参数还与 HSP70-2 rs1061581 多态性有关,该多态性与多发性硬化症的发病风险相关。此外,线粒体活性和 HSP70-2 蛋白水平也与疾病的严重程度有关。总之,我们的研究结果表明,多发性硬化症患者和健康对照组的白细胞介导细胞对氧化损伤的反应相似;在这种情况下,HSP70-2 似乎不是保护白细胞介导细胞的核心。然而,HSP70-2 rs1061581 多态性与 ROS 水平有关,似乎在氧化刺激下 HSP70-2 的不同表达中起了作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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