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Macrophages derived from C3H/HeJ ( Lps d ) mice respond to bacterial lipopolysaccharide by activating NF‐ χ B
Author(s) -
Ding Aihao,
Hwang Sonya,
Lander Harry M.,
Xie Qiaowen
Publication year - 1995
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1002/jlb.57.1.174
Subject(s) - lipopolysaccharide , biology , macrophage , tumor necrosis factor alpha , nitric oxide , microbiology and biotechnology , transcription factor , nf κb , p50 , gene expression , electrophoretic mobility shift assay , gene , signal transduction , biochemistry , immunology , in vitro , endocrinology
The effects of bacterial lipopolysaccharide (LPS) on macrophage gene expression are mediated in part by its ability to induce activation of transcription factor NF‐χB. We compared the ability of LPS‐treated macrophages from Lps n (LPS‐responsive) C3H/HeN and Lps d (LPS‐hyporesponsive) C3H/HeJ mice to mobilize NF‐ χ B by electrophoretic mobility shift assays with oligonucleotide probes containing a unique NF‐ χ B sequence from the promoter of inducible nitric oxide synthase (iNOS). In response to ng/ml concentrations of LPS, this probe bound proteins that appeared rapidly in the nuclei of thioglycollate‐elicited macrophages and bone marrow–derived macrophage cell lines from both Lps n and Lps d mice. Only in macrophages from Lps n mice, however, was LPS able to induce iNOS or tumor necrosis factor α. NF‐ χ B‐containing DNA‐protein complexes from Lps d macrophages were formed in lesser amounts than from Lps n macrophages but shared the same composition, insofar as they displayed the same electrophoretic mobilities and content of heterodimers of p50/RelA (p65) and p50/c‐rel. Two conclusions emerge from these findings: (1) NF‐ χ B activity alone is not sufficient for induction of certain LPS‐responsive genes and (2) An LPS‐response pathway involving activation of NF‐ χ B is preserved in Lps d mice. The inability of cells from Lps d mice to induce gene expression in response to LPS thus cannot be attributed to inability to activate NF‐ χ B. J. Leukoc. Biol. 57: 174–179; 1995.

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