摘要
在脂多糖(LPS)诱导的细胞信号转导过程中,髓样分化蛋白-2(MD-2)与LPS和Toll样受体4(TLR4)分别结合,发挥桥梁分子的作用,介导TLR4对LPS的识别。LPS是与MD-2结合,而不是TLR4,没有MD-2的参与,细胞也不能发生反应或反应微弱。MD-2可被分泌到血浆中,形成可溶性的MD-2,对只含有TLR4而无MD-2的细胞进行远程调控。表明MD-2在转导内毒素信号中具有重要作用。MD-2具有分子质量小、核酸片段短、便于调控等特点,是极具潜力的新型抗炎靶点。
Myeloid differentiation protein-2(MD-2)can separately and simultaneously bind lipopolysaccharide(LPS)and toll-like receptor 4(TLR4)has been shown to play critical roles in mediated recognition responses to LPS by TLR4 and signal transduction induced by LPS.MD-2 can be bound by LPS,not TLR4.The cells have no responsiveness or weak responsiveness to LPS without MD-2.MD-2 can be secreted into blood plasma,formed soluble MD-2 and remotely regulated cells that contained TLR4 without MD-2.MD-2 has been shown to play important roles in endotoxin signal transduction.MD-2 is a small molecular,short nucleic acid fragment,easily regulated should become a new potential anti-inflammatory target.
出处
《实用儿科临床杂志》
CAS
CSCD
北大核心
2010年第6期451-454,共4页
Journal of Applied Clinical Pediatrics
基金
四川省科技厅科研基金项目(05JY029-054-2)
关键词
髓样分化蛋白-2
脂多糖
TOLL样受体4
信号转导
感染
婴儿
新生
myeloid differentiation protein-2
lipopolysaccharide
toll-like receptor 4
signal transduction
infection
infant
newborn