Literature DB >> 14636836

Toll-like receptor 4-dependent activation of macrophages by polysaccharide isolated from the radix of Platycodon grandiflorum.

Yeo Dae Yoon1, Sang Bae Han, Jong Soon Kang, Chang Woo Lee, Song-Kyu Park, Hyun Sun Lee, Jong Seong Kang, Hwan Mook Kim.   

Abstract

Platycodon grandiflorum, a traditional oriental herbal medicine, is known to have immunostimulatory and antitumor effects. PG, a polysaccharide isolated from P. grandiflorum, has been reported to activate macrophages and B cells. Here, we investigated the membrane receptor and intracellular signaling responsible for the activation of macrophages by PG. PG induced the production of nitric oxide (NO) and the mRNA expression of iNOS in RAW 264.7 cells. To investigate the membrane receptor involved in the activation of NO production, we examined the effect of PG on the production of NO in mouse peritoneal macrophages isolated from wild type C3H/HeN and functional Toll-like receptor 4 (TLR4)-deficient C3H/HeJ mice. PG induced NO production by macrophages isolated from C3H/HeN mice, but had no effect on NO production by macrophages isolated from C3H/HeJ mice. Moreover, monoclonal antibodies directed to TLR4 blocked PG-mediated induction of NO production. In addition, LBP and sCD14 was also found to be involved in the activation of NO production by PG. To further investigate, we examined the effect of PG on the activation of DNA binding of NF-kappa B, which is a downstream transcriptional regulator of TLR4. PG caused degradation of I kappa B and activation of DNA binding of NF-kappa B. In addition, TPCK, a specific NF-kappa B inhibitor, abolished PG-mediated induction of DNA binding of NF-kappa B, production of NO and mRNA expression of iNOS, demonstrating the involvement of NF-kappa B in PG-mediated macrophage activation. Taken together, these results suggest that PG-mediated induction of NO production and iNOS mRNA expression in macrophages is mediated, at least in part, by TLR4/NF-kappa B signaling pathway.

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Year:  2003        PMID: 14636836     DOI: 10.1016/j.intimp.2003.09.005

Source DB:  PubMed          Journal:  Int Immunopharmacol        ISSN: 1567-5769            Impact factor:   4.932


  23 in total

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