Induction of a type I interferon signature in normal human monocytes by gadolinium‐based contrast agents: comparison of linear and macrocyclic agents
Author(s) -
Wermuth P. J.,
Jimenez S. A.
Publication year - 2014
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/cei.12211
Subject(s) - monocyte , chemokine , proinflammatory cytokine , fibrosis , nephrogenic systemic fibrosis , immunology , interferon , biology , inflammation , fibronectin , microbiology and biotechnology , pathology , medicine , endocrinology , extracellular matrix , kidney disease
Summary The gadolinium‐based contrast agent ( GdBCA ) O mniscan activates human macrophages through Toll‐like receptor ( TLR)‐ 4 and TLR‐ 7 signalling. To explore the mechanisms responsible we compared the ability of linear and macrocyclic GdBCA to induce a type I interferon signature and a proinflammatory/profibrotic phenotype in normal human monocytes in vitro . Expression of genes associated with type I interferon signalling and inflammation and production of their corresponding proteins were determined. Both linear and macrocyclic GdBCA stimulated expression of multiple type I interferon‐regulated genes and the expression of numerous chemokines, cytokines and growth factors in normal human peripheral blood monocytes. There was no correlation between the magnitude of the measured response and the G d chelate used. To explore the mechanisms responsible for GdBCA induction of fibrosis in nephrogenic systemic fibrosis ( NSF ) in vitro , normal human dermal fibroblasts were incubated with GdBCA ‐treated monocyte culture supernatants and the effects on profibrotic gene expression were examined. Supernatants from monocytes exposed to all GdBCA stimulated types I and III collagen, fibronectin and α‐smooth muscle actin (α‐ SMA) expression in normal dermal fibroblasts. The results indicate that the monocyte activation induced by GdBCA may be the initial step in the development of GdBCA associated fibrosis in NSF .
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