Murine neutrophils treated with alphaB‐crystallin reduce IL‐12p40 production by dendritic cells. Issue 1 (17th April 2018)

• Record Type: Journal Article
• Authors: Finlay, Trisha M.; Palmer, Alexandra L.; Ousman, Shalina S.
• Is Part Of: Immunology. Volume 155:Issue 1(2018)
• Page Start: 72
• Page End: 84
• Publication Date: 2018-04-17
• Subjects: alphaB‐crystallin -- dendritic cells -- interleukin‐10 -- interleukin‐12 -- matrix metalloproteinases; Immunology -- Periodicals
• DOI: 10.1111/imm.12924
• Languages: English
• ISSNs: 0019-2805

Abstract

Summary: Neutrophils are essential in the fight against invading pathogens. They utilize antimicrobial effector mechanisms, such as phagocytosis, release of proteases and other antimicrobial products, robust oxidative bursts and neutrophil extracellular traps to combat infections. Neutrophils also modulate immune responses through the production of eicosanoids, cytokines and chemokines, as well as via direct communication with other immune cells. This system of high‐intensity offense against pathogens is exquisitely balanced through regulation to limit damage to host tissue. Unfortunately, the control of neutrophils is not failproof. In cases of sterile injury, autoimmunity and even during an infection, neutrophils can cause tissue destruction and become detrimental to the host. For that reason, there is a need to find means to regulate the aberrant activation of these cells. We found that alphaB‐crystallin ( α BC), a heat‐shock protein known to have anti‐inflammatory abilities, affects certain properties of mouse neutrophils that subsequently influence the pro‐inflammatory state of antigen‐presenting cells (APCs). More specifically, α BC mediated small but significant increases in the levels of IL‐10 and matrix metalloproteinase 8, and altered hydrogen peroxide secretion by stimulated neutrophils. Further, the heat‐shock protein influenced the communication between neutrophils and dendritic cells by decreasing the production of pro‐inflammatory cytokines, specifically IL‐12p40, by the APCs. α BC could thus contribute to dampening neutrophil inflammatory responses by impacting the effect of neutrophils on other immune cells. Abstract : Neutrophils are essential for protection from pathogens, but their effector functions and ability to modulate the responses of other immune cells such as dendritic cells have to be tightly controlled as exuberant infiltration and activation of neutrophils during sterile injury, autoimmunity or infection can lead to tissue damage. We found that the small heat‐shock protein alphaB‐crystallin ( α BC) mediated a small increase in IL‐10 and MMP8 production by neutrophils, and that α BC‐treated neutrophils reduced the production of IL‐12p40 by DCs in both a contact‐ and non‐contact‐dependent manner.