Zubova S V, Radzyukevich Ya V, Kosyakova N I, Prokhorenko I R
Institute for Biological Instrumentation, Federal Research Center Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences, Pushchino, 142290 Russian Federation.
Institute of Basic Biological Problems, Federal Research Center Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences, Pushchino, 142290 Russian Federation.
Acta Naturae. 2025 Jan-Mar;17(1):106-109. doi: 10.32607/actanaturae.27555.
TLR2 and TLR4 play a key role in the development of an inflammation in response to a bacterial infection. We studied the effect of PG lipopolysaccharide (LPS) on proinflammatory cytokine synthesis activation by the TLR2 and TLR4 agonists LPS, lipoteichoic acid (LTA), and Pam3CSK4 (a synthetic bacterial lipopeptide) in human whole blood cells. PG LPS was shown to exhibit antagonistic properties against the studied TLR4 and TLR2 agonists, blocking the synthesis of the cytokines TNF-α, IL-6, and IL-8. Possible mechanisms behind the suppressing effect of PG LPS are proposed. PG LPS can serve as a prototype for drugs against both gram-negative and gram-positive bacteria.
Toll样受体2(TLR2)和Toll样受体4(TLR4)在细菌感染引发的炎症反应中发挥关键作用。我们研究了PG脂多糖(LPS)对人全血细胞中TLR2和TLR4激动剂脂多糖(LPS)、脂磷壁酸(LTA)及Pam3CSK4(一种合成细菌脂肽)诱导的促炎细胞因子合成激活的影响。结果表明,PG LPS对所研究的TLR4和TLR2激动剂具有拮抗特性,可阻断细胞因子肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和白细胞介素-8(IL-8)的合成。文中提出了PG LPS抑制作用背后的可能机制。PG LPS可作为抗革兰氏阴性菌和革兰氏阳性菌药物的原型。