Impairment of Mitochondrial Redox Status in Peripheral Lymphocytes of Multiple Sclerosis Patients

Author

Gonzalo Benito, Hugo

Nogueras Penabad, Lara

Gil-Sánchez, Anna

Vicente Hervás, José

Valcheva, Petya

González Mingot, Cristina

Martín Garí, Meritxell

Canudes Solans, Marc

Peralta Moncusí, Silvia

Solana Moga, M. José

Pamplona Gras, Reinald

Portero Otín, Manuel

Boada Pallàs, Jordi

Serrano Casasola, José Carlos Enrique

Brieva Ruiz, Luis

Publication date

2020-03-09T09:52:59Z

2020-03-09T09:52:59Z

2019



Abstract

Literature suggests that oxidative stress (OS) may be involved in the pathogenesis of multiple sclerosis (MS), in which the immune system is known to play a key role. However, to date, the OS in peripheral lymphocytes and its contribution to the disease remain unknown. The aim of the present study was to explore the influence of OS in peripheral lymphocytes of MS patients. To that end, a cross-sectional, observational pilot study was conducted [n = 58: 34 MS and 24 healthy subjects (control group)]. We have measured superoxide production and protein mitochondrial complex levels in peripheral blood mononuclear cells (PBMCs) isolated from MS patients and control. Lactate levels and the antioxidant capacity were determined in plasma. We adjusted the comparisons between study groups by age, sex and cell count according to case. Results demonstrated that PBMCs, specifically T cells, from MS patients exhibited significantly increased superoxide anion production compared to control group (p = 0.027 and p = 0.041, respectively). Increased superoxide production in PBMCs was maintained after the adjustment (p = 0.044). Regarding mitochondrial proteins, we observe a significant decrease in the representative protein content of the mitochondrial respiratory chain complexes I-V in PBMCs of MS patients (p = 0.002, p = 0.037, p = 0.03, p = 0.044, and p = 0.051, respectively), which was maintained for complexes I, III, and V after the adjustment (p = 0.026; p = 0.033; p = 0.033, respectively). In MS patients, a trend toward increased plasma lactate concentration was detected [8.04 mg lactate/dL (5.25, 9.49) in the control group, 11.36 mg lactate/dL (5.41, 14.81) in MS patients] that was statistically significant after the adjustment (p = 0.013). This might be indicative of compromised mitochondrial function. Finally, antioxidant capacity was also decreased in plasma from MS patients, both before (p = 0.027) and after adjusting for sex and age (p = 0.006). Our findings demonstrate that PBMCs of MS patients show impaired mitochondrial redox status and deficient antioxidant capacity. These results demonstrate for the first time the existence of mitochondrial alterations in the cells immune cells of MS patients already at the peripheral level.


We acknowledge funding from the Biogen Idec Laboratories (ES-TYS-13-10491), the Spanish Ministry of Economy and Competitiveness (PI-1400328), the Autonomous Catalonia Government (ref. 20145GR1681), the Spanish Network of Multiple Sclerosis (REEM) managed by the Carlos III Health Institute (ISCIII) exp. RD16/0015/0008, and FEDER funds from the European Union (“a way to build Europe”).

Document Type

Article
Published version

Language

English

Subjects and keywords

Multiple sclerosis; Oxidative stress; Mitochondria; Superoxide anion; Mitochondrial complexes

Publisher

Frontiers Media

Related items

Reproducció del document publicat a https://doi.org/10.3389/fnins.2019.00938

Frontiers in Neuroscience, 2019, vol. 13

Rights

cc-by, (c) Gonzalo et al., 2019

http://creativecommons.org/licenses/by/4.0/

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