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An invertebrate TNF functional analogue activates macrophages via lectin-saccharide interaction with ion channels
Author(s) -
Martin Bilej,
Radka Josková,
Rafaël Van den Bergh,
Petra Procházková,
Marcella Silerova,
Paul Ameloot,
Patrick De Baetselier,
Alain Beschin
Publication year - 2006
Publication title -
international immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.86
H-Index - 134
eISSN - 1460-2377
pISSN - 0953-8178
DOI - 10.1093/intimm/dxl100
Subject(s) - lectin , tumor necrosis factor alpha , microbiology and biotechnology , innate immune system , macrophage , cytokine , chemistry , cytolysis , biology , galectin , nitric oxide , immune system , secretion , immunology , biochemistry , in vitro , cytotoxicity , endocrinology
The invertebrate pattern-recognition protein named coelomic cytolytic factor (CCF) and the mammalian cytokine tumor necrosis factor (TNF) share functional analogies that are based on a similar saccharide recognition specificity. In particular, CCF and TNF have been shown to interact with ion channels on the surface of vertebrate cells via N,N'-diacetylchitobiose lectin-like activity. In the present study, we show that CCF-induced membrane depolarization results in the release of TNF, IL-6 and nitric oxide (NO) by macrophages via nuclear factor-kappaB signaling. Interestingly, our data suggest that TNF contributes, through lectin-saccharide interaction, to the secretion of IL-6 and NO induced by CCF. This experimental non-physiological setting based on the interaction of an invertebrate defense lectin with vertebrate cells involved in the innate immune response may have highlighted an evolutionarily ancient mechanism of macrophage activation in vertebrates.

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