Endotoxin-Binding Peptides Derived from Casein Glycomacropeptide Inhibit Lipopolysaccharide-Stimulated Inflammatory Responses via Blockade of NF-κB activation in macrophagesReportar como inadecuado




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1

Key Laboratory of Functional Dairy, College of Food Science and Nutritional Engineering, China Agriculture University, Beijing 100083, China

2

Key Laboratory of Space Nutrition and Food Engineering, China Astronaut Training Center, Beijing 100094, China

3

Synergetic Innovation Center of Food Safety and Nutrition, Northeast Agriculture University, Haerbin 150030, China





*

Author to whom correspondence should be addressed.



Abstract Systemic low-grade inflammation and increased circulating lipopolysaccharide LPS contribute to metabolic dysfunction. The inhibitory effects and underlying molecular mechanisms of casein glycomacropeptide GMP hydrolysate on the inflammatory response of LPS-stimulated macrophages were investigated. Results showed that the inhibitory effect of GMP hydrolysates obtained with papain on nitric oxide NO production were obviously higher than that of GMP hydrolysates obtained with pepsin, alcalase and trypsin p < 0.05, and the hydrolysate obtained with papain for 1 h hydrolysis GHP exhibited the highest inhibitory effect. Compared with native GMP, GHP markedly inhibited LPS-induced NO production in a dose-dependent manner with decreased mRNA level of inducible nitric oxide synthase iNOS. GHP blocked toll-like receptor 4 TLR4-myeloid differentiation primary response 88 MyD88-nuclear factor-κB NF-κB signaling pathway activation, accompanied by downregulation of LPS-triggered significant upregulation of tumor necrosis factor TNF-α and interleukin IL-1β gene expression. Furthermore, GHP could neutralize LPS not only by direct binding to LPS, but also by inhibiting the engagement of LPS with the TLR4-MD2 complex, making it a potential LPS inhibitor. In conclusion, these findings suggest that GHP negatively regulates TLR4-mediated inflammatory response in LPS-stimulated RAW264.7 cells, and therefore may hold potential to ameliorate inflammation-related issues. View Full-Text

Keywords: casein glycomacropeptide; LPS-binding; inflammation; toll-like receptor 4; nuclear factor-κB casein glycomacropeptide; LPS-binding; inflammation; toll-like receptor 4; nuclear factor-κB





Autor: Xue Cheng 1,2, Dongxiao Gao 1, Bin Chen 3 and Xueying Mao 1,*

Fuente: http://mdpi.com/



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