Manabe H, Utsumi H, Kusama T, Hamada A
Department of Health Chemistry, School of Pharmaceutical Science, Showa University, Tokyo.
J Biochem. 1989 Jun;105(6):861-3. doi: 10.1093/oxfordjournals.jbchem.a122767.
The immunopotentiating property of spin-labeled lipophilic muramyl dipeptide (SL-MDP) in liposomes was studied as to the plaque-forming cell (PFC) response to glycophorin, as an antigen, in membranes. The effect of SL-MDP depended on the densities of both SL-MDP itself and the antigen. The addition of the optimal amount of SL-MDP to liposomes containing a low density (0.016 mol%) of the antigen increased the PFC response by three times, whereas the presence of SL-MDP in optimal antigen density (0.032 0.127 mol%) membranes was rather inhibitory. In these liposomes, the amounts and molecular states of SL-MDP were determined from ESR spectra and are discussed in connection with its immunopotentiating property.
研究了脂质体中自旋标记的亲脂性胞壁酰二肽(SL-MDP)的免疫增强特性,该特性与作为膜中抗原的血型糖蛋白的空斑形成细胞(PFC)反应有关。SL-MDP的作用取决于SL-MDP自身以及抗原的密度。向含有低密度(0.016摩尔%)抗原的脂质体中添加最佳量的SL-MDP可使PFC反应增加三倍,而在最佳抗原密度(0.032 - 0.127摩尔%)的膜中存在SL-MDP则具有相当大的抑制作用。在这些脂质体中,通过电子自旋共振光谱确定了SL-MDP的量和分子状态,并结合其免疫增强特性进行了讨论。