iNOS dependent and independent phases of lymph node expansion in mice with TNF-induced inflammatory-erosive arthritis.
Academic Article
Overview
abstract
INTRODUCTION: A pivotal effect of lymphatic vessel (LV) function in joint homeostasis was identified in the tumor necrosis factor-transgenic (TNF-Tg) mouse model of rheumatoid arthritis (RA). Specifically, loss of LV contractions is associated with progressive synovitis and erosions. Furthermore, draining lymph node expansion is a biomarker of arthritic progression, and both macrophages and lymphatic endothelial cells express inducible nitric oxide synthase (iNOS), which disrupts LV contraction and transport of immune cells to the draining lymph nodes. Therefore, to directly assess these relationships, we tested the hypothesis that TNF-Tg mice with global genetic ablation of iNOS (iNOS-/-) will show delayed draining lymph node expansion, maintained LV contractions, and decreased synovitis and erosions. METHOD: iNOS-/-× TNF-Tg female and male mice, and control littermates (iNOS-/-, TNF-Tg, and WT), were examined with (1) ultrasound to determine popliteal lymph node (PLN) volume and (2) near-infrared imaging (NIR) to assess popliteal LV contraction frequency, and differences between genotypes were assessed at 3, 4, 5, and 6 months of age. Knees and PLN were harvested at 4 months in females and 6 months in males, to assess synovitis, bone erosions, and cellular accumulation in PLN sinuses via histology. RESULTS: Initially, an increase in PLN volume was observed for both female and male iNOS-/-× TNF-Tg and TNF-Tg compared to their WT and iNOS-/- counterparts at 2 and 3 months, respectively. Subsequently, TNF-Tg PLNs continue to increase in volume, while iNOS-/-× TNF-Tg did not increase in volume from the initial timepoints. WT and iNOS-/- PLN volume was unchanged throughout the experiment. LV contraction frequency was increased at 4 months in females and 5 months in males, in the iNOS-/-× TNF-Tg mice compared to the TNF-Tg. Synovitis and erosions were moderately reduced in iNOS-/-× TNF-Tg versus TNF-Tg knees in females, while no differences in knee pathology were observed in males. CONCLUSIONS: Genetic iNOS ablation maintains draining lymph node volume and LV function during TNF-induced inflammatory arthritis and is associated with moderately decreased joint inflammation and damage.
