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Distinct regulation by lipopolysaccharides of the expression of interleukin-1β by murine macrophages and salivary glands
Author(s) -
Seil M,
Ouaaliti M El,
Abdou Foumekoye S,
Pochet S,
Dehaye JP
Publication year - 2012
Publication title -
innate immunity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.921
H-Index - 69
eISSN - 1743-2839
pISSN - 1753-4259
DOI - 10.1177/1753425910377101
Subject(s) - submandibular gland , endocrinology , medicine , secretion , pilocarpine , saliva , cytokine , cd14 , salivary gland , interleukin , chemistry , biology , microbiology and biotechnology , receptor , neuroscience , epilepsy
The regulation of interleukin (IL)-1 expression and secretion by salivary glands and macrophages in response to lipopolysaccharides (LPS) was compared. In wild-type mice, injection of LPS significantly decreased the volume of saliva stimulated by pilocarpine and increased its protein and amylase concentration. It did not modify the salivary concentration of IL-1β. The cytokine was expressed by submandibular acini and ducts. Macrophages also expressed IL-1β but at lower concentration than salivary glands. The pre-incubation of macrophages with LPS increased the phosphorylation of IκB and the expression of IL-1β. Adenosine triphosphate also promoted the secretion of the cytokine by these cells. These responses were absent in submandibular gland cells. These glands expressed CD14, TLR4 and MyD88. P2X 7 -KO mice secreted a lower volume of saliva which contained less proteins and amylase. In conclusion, IL-1β is constitutively expressed by submandibular glands and its secretion is not regulated by a P2X 7 agonist. In these cells, LPS do not activate the nuclear factor-κB–pro-IL-1β axis in spite of the expression of the proteins involved in their recognition.

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