Effect of lipopolysaccharide binding protein gene polymorphism on lipopolysaccharide-induced LBP and inflammatory cytokine levels
Yao Yongming
Abstract
Yao Yongming
Abstract
Objective To evaluate whether the lipopolysaccharide binding protein (LBP) C1306→T single nucleotide polymorphism influences the LBP and inflammatory cytokine levels in whole blood culture. Methods In 118 healthy human blood donors, the C1306→T gene polymorphism was determined by using polymerase chain reaction and subsequent Stu I restriction enzyme digestion of the polymerase chain reaction products. Supernatant concentrations of LBP, TNF-α, IL-6 and IL-10 were measured by using a whole blood cell culture model in the presence or absence of lipopolysaccharide ( LPS) stimulation. Results Among the 118 individuals, 14 subjects were heterozygous and 104 homozygous for the T/T allele.The LBP levels in supernatant were higher in T/C heterozygotes than in the individuals homozygous for the T allele either before or after LPS stimulation, while no marked correlations were found between LBP C1306→T polymorphism and TNF-α, IL-6 or IL-10 formation to LPS (P 0.05).Conclusion The LBP C1306→T polymorphism may influence the LBP level indirectly, but did not significantly relate to inflammatory cytokine in vitro.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To evaluate whether the lipopolysaccharide binding protein (LBP) C1306→T single nucleotide polymorphism influences the LBP and inflammatory cytokine levels in whole blood culture. Methods In 118 healthy human blood donors, the C1306→T gene polymorphism was determined by using polymerase chain reaction and subsequent Stu I restriction enzyme digestion of the polymerase chain reaction products. Supernatant concentrations of LBP, TNF-α, IL-6 and IL-10 were measured by using a whole blood cell culture model in the presence or absence of lipopolysaccharide ( LPS) stimulation. Results Among the 118 individuals, 14 subjects were heterozygous and 104 homozygous for the T/T allele.The LBP levels in supernatant were higher in T/C heterozygotes than in the individuals homozygous for the T allele either before or after LPS stimulation, while no marked correlations were found between LBP C1306→T polymorphism and TNF-α, IL-6 or IL-10 formation to LPS (P 0.05).Conclusion The LBP C1306→T polymorphism may influence the LBP level indirectly, but did not significantly relate to inflammatory cytokine in vitro.
Key concepts: Lipopolysaccharide binding protein, Lipopolysaccharide, Cytokine, Allele, Polymerase chain reaction, Polymorphism (computer science), Heterozygote advantage, Tumor necrosis factor alpha