TNF-like weak inducer of apoptosis promotes blood brain barrier disruption and increases neuronal cell death in MRL/lpr mice. (June 2015)

• Record Type: Journal Article
• Authors: Wen, Jing; Doerner, Jessica; Weidenheim, Karen; Xia, Yumin; Stock, Ariel; Michaelson, Jennifer S.; Baruch, Kuti; Deczkowska, Aleksandra; Gulinello, Maria; Schwartz, Michal; Burkly, Linda C.; Putterman, Chaim
• Is Part Of: Journal of autoimmunity. Volume 60(2015)
• Page Start: 40
• Page End: 50
• Publication Date: 2015-06
• Subjects: Systemic lupus erythematous (SLE) -- Neuropsychiatric lupus (NPSLE) -- TWEAK -- Fn14; Autoimmunity -- Periodicals; Autoimmune diseases -- Periodicals; Autoantibodies -- Periodicals; Autoimmune Diseases -- Periodicals; Auto-immunité -- Périodiques; Maladies auto-immunes -- Périodiques; Electronic journals; 616.978005
• DOI: 10.1016/j.jaut.2015.03.005
• Languages: English
• ISSNs: 0896-8411

Abstract

Abstract: Neuropsychiatric disease is one of the most common manifestations of human systemic lupus erythematosus, but the mechanisms remain poorly understood. In human brain microvascular endothelial cells in vitro, TNF-like weak inducer of apoptosis (TWEAK) decreases tight junction ZO-1 expression and increases the permeability of monolayer cell cultures. Furthermore, knockout (KO) of the TWEAK receptor, Fn14, in the MRL/lpr lupus mouse strain markedly attenuates neuropsychiatric disease, as demonstrated by significant reductions in depressive-like behavior and improved cognitive function. The purpose of the present study was to determine the mechanisms by which TWEAK signaling is instrumental in the pathogenesis of neuropsychiatric lupus (NPSLE). Evaluating brain sections of MRL/lpr Fn14WT and Fn14KO mice, we found that Fn14KO mice displayed significantly decreased cellular infiltrates in the choroid plexus. To evaluate the integrity of the blood brain barrier (BBB) in MRL/lpr mice, Western blot for fibronectin, qPCR for iNOS, and immunohistochemical staining for VCAM-1/ICAM-1 were performed. We found preserved BBB permeability in MRL/lpr Fn14KO mice, attributable to reduced brain expression of VCAM-1/ICAM-1 and iNOS. Additionally, administration of Fc-TWEAK intravenously directly increased the leakage of a tracer (dextran-FITC) into brain tissue. Furthermore, MRL/lpr Fn14KO mice displayed reduced antibody (IgG) and complement (C3, C6, and C4a) deposition in the brain. Finally, we found that MRL/lpr Fn14KO mice manifested reduced neuron degeneration and hippocampal gliosis. Our studies indicate that TWEAK/Fn14 interactions play an important role in the pathogenesis of NPSLE by increasing the accumulation of inflammatory cells in the choroid plexus, disrupting BBB integrity, and increasing neuronal damage, suggesting a novel target for therapy in this disease. Highlights: The absence of Fn14 decreases inflammation in the choroid plexus of lupus mice. Fn14 deficiency reduces brain expression of VCAM-1, ICAM-1, and iNOS in MRL/lpr. Fc-TWEAK directly increases blood brain barrier permeability in lupus-prone mice. Fn14 deficiency attenuates neuron degeneration and brain cell apoptosis.