Synaptic alterations and immune response are sexually dimorphic in a non-pertussis toxin model of experimental autoimmune encephalomyelitis

• Published in: Experimental neurology 2020-01, Vol.323, p.113061-113061, Article 113061
• Main Authors: Murphy, Kayla L., Fischer, Roman, Swanson, Kathryn A., Bhatt, Ishaan J., Oakley, Laura, Smeyne, Richard, Bracchi-Ricard, Valerie, Bethea, John R.
• Format: Article
• Language: English
• Subjects: Animals; Central nervous system; Chronic neuropathic pain; EAE; Encephalomyelitis, Autoimmune, Experimental - immunology; Encephalomyelitis, Autoimmune, Experimental - pathology; Excitatory signaling; Excitotoxicity; Female; Inflammation; Leukocyte; Male; Mice; Mice, Inbred C57BL; Multiple sclerosis; Sex Characteristics; Sex difference; Synapses - metabolism; Synapses - pathology; Synaptopathy
• ISSN: 0014-4886; 1090-2430
• DOI: 10.1016/j.expneurol.2019.113061

Multiple sclerosis is an autoimmune disorder of the central nervous system (CNS) characterized by locomotor impairments, cognitive deficits, affective disorders, and chronic pain. Females are predominately affected by MS compared to males and develop motor symptoms earlier. However, key symptoms affect all patients regardless of sex. Previous studies have shown that demyelination and axonal damage play key roles in symptom development, but it is unclear why sex differences exist in MS onset, and effective symptom treatment is still lacking. We here used a non-pertussis toxin (nPTX) experimental autoimmune encephalomyelitis (EAE) model in C57BL/6 mice, to explore chronic symptoms and sex differences in CNS autoimmunity. We observed that, like in humans, female mice developed motor disease earlier than males. Further, changes in pre- and post-synaptic protein expression levels were observed in a sexually dimorphic manner with an overall shift towards excitatory signaling. Our data suggest that this shift towards excitatory signaling is achieved through different mechanisms in males and females. Altogether, our study helps to better understand sex-specific disease mechanisms to ultimately develop better diagnostic and treatment tools. •nPTX EAE reflects some aspects female and male MS motor and sensory deficits.•Behavioral deficits are seen in both female and male EAE.•Macrophage-mediated innate immune response is stronger in males.•Synaptic protein expression are sexually dimorphic, but favor excitatory signaling.