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1.
Phytomedicine ; 16(5): 477-84, 2009 May.
Article in English | MEDLINE | ID: mdl-19103478

ABSTRACT

Expression of many pro-inflammatory cytokines is controlled by the NF-kappaB signaling pathway. NF-kappaB is induced by LPS through activation of TLR4. Melanins extracted from fungal, plant and human sources modulate cytokine production and activate NF-kappaB pathway. We showed that a herbal melanin (HM) from Nigella sativa L. modulates cytokine production and suggested it as a ligand for TLR4. In this study we investigated the possibility that the HM-induced cytokine production is via an NF-kappaB signaling pathway. We found that HM induced the degradation of IkappaBalpha, a key step in the activation of NF-kappaB. Moreover, addition of IkappaB kinase (IKK) specific inhibitors effectively inhibited the observed HM-induced production of IL-8 and IL-6 by TLR4-transfected HEK293 cells and THP-1 cells. Our results have also shown that HM induced cleavage of caspase 8, and that this cleavage was partially abrogated by IKK inhibitors. We suggest that HM can modulate the inflammatory response by inducing IL-8 and IL-6 production via TLR4-dependent activation of the NF-kappaB signaling pathway.


Subject(s)
Caspase 8/metabolism , I-kappa B Kinase/antagonists & inhibitors , I-kappa B Proteins/antagonists & inhibitors , Melanins/pharmacology , NF-kappa B/metabolism , Nigella sativa , Toll-Like Receptor 4/metabolism , Apoptosis/drug effects , Cell Line , Humans , Interleukin-6/metabolism , Interleukin-8/metabolism , Lipopolysaccharides/toxicity , Monocytes/drug effects , NF-KappaB Inhibitor alpha , Plant Extracts/pharmacology , Seeds , Signal Transduction/drug effects , Transfection
2.
Anal Biochem ; 356(1): 132-41, 2006 Sep 01.
Article in English | MEDLINE | ID: mdl-16769031

ABSTRACT

A novel, cartridge-based procedure for the efficient and irreversible detritylation of oligonucleotides is reported. This method, combined with a process for the elimination of depurinated fragments produces, in a highly parallel fashion, oligonucleotides with better purity than those traditionally obtained using reversed-phase high-performance liquid chromotography purification. Our combined detritylation and purification methodology compares favorably with commercial cartridge-based purification systems. The benefits of working with pure oligonucleotides, with regard to higher signal and better signal linearity, are shown in array-based hybridization experiments.


Subject(s)
Oligonucleotide Array Sequence Analysis/methods , Oligonucleotides/isolation & purification , Hydrophobic and Hydrophilic Interactions , Oligonucleotide Array Sequence Analysis/statistics & numerical data , Oligonucleotide Probes , Oligonucleotides/chemistry , Reproducibility of Results , Trityl Compounds/chemistry
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