Department of Life System, Institute of Technology and Science, Graduate School, The University of Tokushima, 2-1 Minamijosanjimacho, Tokushima, 770-8506 Japan.
Anticancer Res. 2011 Jul;31(7):2489-92.
The 1f1f subtype of the Gc protein (Gc(1f1f) protein) was converted into Gc-derived macrophage-activating factor (GcMAF) by enzymatic processing in the presence of β-galactosidase of an activated B-cell and sialidase of a T-cell. We hypothesized that preGc(1f1f)MAF, the only Gc(1f1f) protein lacking galactose, can be converted to GcMAF in vivo because sialic acid is cleaved by residual sialidase. Hence, we investigated the effect of preGc(1f1f)MAF on the phagocytic activation of mouse peritoneal macrophages.
We examined the sugar moiety of preGc(1f1f)MAF with a Western blot using peanut agglutinin (PNA) and Helix pomatia agglutinin (HPA) lectin. We also found that preGc(1f1f)MAF significantly enhanced phagocytic activity in mouse peritoneal macrophages but only in the presence of the mouse peritoneal fluid; the level of phagocytic activity was the same as that observed for GcMAF.
PreGc(1f1f)MAF can be used as an effective macrophage activator in vivo.
Gc 蛋白的 1f1f 亚型(Gc(1f1f) 蛋白)在激活 B 细胞的 β-半乳糖苷酶和 T 细胞的唾液酸酶存在下,经酶促加工转化为 Gc 衍生的巨噬细胞激活因子(GcMAF)。我们假设,缺乏半乳糖的唯一 Gc(1f1f) 蛋白 preGc(1f1f)MAF 可以在体内转化为 GcMAF,因为唾液酸被残留的唾液酸酶裂解。因此,我们研究了 preGc(1f1f)MAF 对小鼠腹腔巨噬细胞吞噬激活的影响。
我们使用花生凝集素(PNA)和榛实凝集素(HPA)凝集素来检测 preGc(1f1f)MAF 的糖基部分。我们还发现 preGc(1f1f)MAF 显著增强了小鼠腹腔巨噬细胞的吞噬活性,但仅在存在小鼠腹腔液的情况下才有效;吞噬活性水平与 GcMAF 观察到的水平相同。
PreGc(1f1f)MAF 可作为体内有效的巨噬细胞激活剂。