Increased Serum Levels of Brain-Derived Neurotrophic Factor Contribute to Inflammatory Responses in Patients with Rheumatoid Arthritis

The aim of this study is to investigate the role of brain-derived neurotrophic factor (BDNF) in the inflammatory responses in patients with rheumatoid arthritis (RA). Serum levels of BDNF and the precursor form of BDNF (proBDNF) from 625 RA patients and 40 controls were analyzed using enzyme-linked immunosorbent assay. Effects of BDNF on the mitogen-activated protein kinase pathway were analyzed by Western blotting. Microarray analysis was conducted to search BDNF regulated gene expression in Jurkat cells, and the differentially expressed genes were validated using T cells from patients with RA and controls. Serum BDNF levels were significantly elevated in patients with RA compared with the controls. Low serum BDNF levels were found in RA patients with anxiety or receiving biologics treatment. BDNF (20 ng/mL) enhanced the phosphorylation of ERK, JNK, and c-Jun, but suppressed the phosphorylation of p38, whereas BDNF (200 ng/mL) enhanced the phosphorylation of ERK and p38. After validation, the expression of CAMK2A, MASP2, GNG13, and MUC5AC, regulated by BDNF and one of its receptors, NGFR, was increased in RA T cells. BDNF increased the IL-2, IL-17, and IFN-gamma expression in Jurkat cells and IL-2 and IFN-gamma secretion in activated peripheral blood mononuclear cells.

Automated summary

This study found that serum BDNF levels were significantly elevated in RA patients compared to controls, with lower levels in patients with anxiety or receiving biologics treatment. BDNF had varying effects on different MAPK pathways and regulated the expression of multiple genes, leading to increased expression of specific genes in RA patient T cells. BDNF also increased the expression of inflammatory cytokines in Jurkat cells and secretion of IL-2 and IFN-gamma in activated peripheral blood mononuclear cells.