Chemically-modified polysaccharide extract derived from Leucaena leucocephala alters Raw 264.7 murine macrophage functions

被引:43
作者
Gamal-Eldeen, Amira M. [1 ]
Amer, Hassan
Helmy, Wafaa A.
Talaat, Roba M.
Ragab, Halla
机构
[1] Natl Res Ctr, Genet Engn & Biotechnol Div, Dept Biochem, Nobel Project,Canc Biol Lab, Cairo 12622, Egypt
[2] Natl Res Ctr, Dept Nat & Microbial Prod Chem, Cairo 12622, Egypt
关键词
Leucaena leucocephala; macrophage; nitric oxide; tumor necrosis factor; LPS binding; phagocytosis;
D O I
10.1016/j.intimp.2007.02.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this study, a chemical modification of the polysaccharides extract (E) derived from Leucaena leucocephala seeds was performed to prepare C-glycosidic 2-propanol derivative (PE), and its sulphated derivative (SPE). This study aimed to characterize immunomodulatory activities of the original extract and its derivatives by exploring their effects on Raw macrophage 264.7 functions and their antioxidant activity. Our results indicated that PE was an effective radical scavenger to hydroxyl, peroxyl, and superoxide anion radicals, and SPE was a peroxyl radical scavenger. PE and SPE were found to influence the macrophage functions. Both of PE and SPE enhanced the macrophage proliferation and phagocytosis of FITC-zymosan; PE inhibited nitric oxide (NO) generation and tumor necrosis factor-a (TNF-a.) secretion in lipopolysaccharide (LPS)-stimulated Raw macrophage 264.7. In contrast, SPE over-induced NO generation and TNF-alpha secretion. Moreover, PE strongly inhibited the binding affinity of FITC-LPS to Raw 264.7, as indicated by flow cytometry analysis. These findings revealed that PE may act as a potent antiinflammatory agent; however SPE may act as an inducer of macrophage functions against pathogens. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:871 / 878
页数:8
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