IL-6 signaling mediates the germinal center response, IgM production and nociceptive sensitization in male mice after tibia fracture
WW Li, Y Yang, TZ Guo, P Sahbaie, X Shi… - Brain, behavior, and …, 2021 - Elsevier
WW Li, Y Yang, TZ Guo, P Sahbaie, X Shi, Q Guang, WS Kingery, LA Herzenberg, JD Clark
Brain, behavior, and immunity, 2021•ElsevierBackground Up-regulated interleukin 6 (IL-6) signaling, immune system activation, and
pronociceptive autoantibodies are characteristic of complex regional pain syndrome
(CRPS). IL-6 is known to promote B cell differentiation, thus we hypothesized that IL-6
signaling plays a crucial role in the development of adaptive immune responses and
nociceptive sensitization in a murine tibia fracture model of CRPS. Methods Mice deficient in
IL-6 expression (IL-6−/−) or B cell deficient (muMT) underwent tibia fracture and 3 weeks of …
pronociceptive autoantibodies are characteristic of complex regional pain syndrome
(CRPS). IL-6 is known to promote B cell differentiation, thus we hypothesized that IL-6
signaling plays a crucial role in the development of adaptive immune responses and
nociceptive sensitization in a murine tibia fracture model of CRPS. Methods Mice deficient in
IL-6 expression (IL-6−/−) or B cell deficient (muMT) underwent tibia fracture and 3 weeks of …
Background
Up-regulated interleukin 6 (IL-6) signaling, immune system activation, and pronociceptive autoantibodies are characteristic of complex regional pain syndrome (CRPS). IL-6 is known to promote B cell differentiation, thus we hypothesized that IL-6 signaling plays a crucial role in the development of adaptive immune responses and nociceptive sensitization in a murine tibia fracture model of CRPS.
Methods
Mice deficient in IL-6 expression (IL-6−/−) or B cell deficient (muMT) underwent tibia fracture and 3 weeks of cast immobilization or sham injury. The deposition of IgM in fractured limbs was followed using Western blotting, and passive serum transfer to muMT fracture mice was used to detect nociception-supporting autoantibodies. Lymph nodes were assessed for hypertrophy, IL-6 expression was measured using qPCR and ELISA, and germinal center formation was evaluated using FACS and immunohistochemistry. The therapeutic effects of exogenous neutralizing anti-IL-6 antibodies were also evaluated in the CRPS fracture model.
Results
Functional IL-6 signaling was required for the post fracture development of nociceptive sensitization, vascular changes, and IgM immune complex deposition in the skin of injured limbs. Passive transfer of sera from wild-type, but not IL-6−/− fracture mice into muMT fracture mice caused enhanced allodynia and postural unweighting. IL-6−/− fracture mice displayed reduced popliteal lymphadenopathy after fracture. Germinal center responses were detected in the popliteal lymph nodes of wild-type, but not in IL-6−/− fracture mice. We observed that IL-6 expression was dramatically enhanced in popliteal lymph node tissue after fracture. Conversely, administration of anti-IL-6 antibodies reduced nociceptive and vascular changes after fracture and inhibited lymphadenopathy.
Conclusions
Collectively, these data support the hypothesis that IL-6 signaling in the fracture limb of mice is required for germinal center formation, IgM autoantibody production and nociceptive sensitization. Anti-IL-6 therapies might, therefore, reduce pain after limb fracture or in the setting of CRPS.
Elsevier
