Toll‐like receptor‐mediated inhibition of Gas6 and ProS expression facilitates inflammatory cytokine production in mouse macrophages

T Deng, Y Zhang, Q Chen, K Yan, D Han - Immunology, 2012 - Wiley Online Library
T Deng, Y Zhang, Q Chen, K Yan, D Han
Immunology, 2012Wiley Online Library
Activation of Toll‐like receptors (TLRs) triggers rapid inflammatory cytokine production in
various cell types. The exogenous product of growth‐arrest‐specific gene 6 (Gas6) and
Protein S (ProS) inhibit the TLR‐triggered inflammatory responses through the activation of
Tyro3, Axl and Mer (TAM) receptors. However, regulation of the Gas6/ProS‐TAM system
remains largely unknown. In the current study, mouse macrophages are shown to
constitutively express Gas6 and ProS, which synergistically suppress the basal and TLR …
Summary
Activation of Toll‐like receptors (TLRs) triggers rapid inflammatory cytokine production in various cell types. The exogenous product of growth‐arrest‐specific gene 6 (Gas6) and Protein S (ProS) inhibit the TLR‐triggered inflammatory responses through the activation of Tyro3, Axl and Mer (TAM) receptors. However, regulation of the Gas6/ProS‐TAM system remains largely unknown. In the current study, mouse macrophages are shown to constitutively express Gas6 and ProS, which synergistically suppress the basal and TLR‐triggered production of inflammatory cytokines, including those of tumour necrosis factor‐α, interleukin‐6 and interleukin‐1β, by the macrophages in an autocrine manner. Notably, TLR signalling markedly decreases Gas6 and ProS expression in macrophages through the activation of the nuclear factor‐κB. Further, the down‐regulation of Gas6 and ProS by TLR signalling facilitates the TLR‐mediated inflammatory cytokine production in mouse macrophages. These results describe a self‐regulatory mechanism of TLR signalling through the suppression of Gas6 and ProS expression.
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