Johnson E, Bøgwald J, Eskeland T, Seljelid R
Scand J Immunol. 1983 May;17(5):403-10. doi: 10.1111/j.1365-3083.1983.tb00806.x.
We have determined the receptors on human monocytes and mouse peritoneal macrophages producing agarose binding. By using isolated human complement factors C3, B and D, agarose beads were coated with C3b. In some experiments C3b was converted to C3bi by using human serum diluted 1:20. Agarose beads coated with C3b or C3bi bound strongly to monocytes. Only agarose beads coated with C3bi were attached to mouse macrophages. Trypsinization of agarose beads coated with C3bi abolished the attachment of the beads to macrophages and monocytes, probably because of conversion of C3bi to C3d. Endocytosis by macrophages of agarose preincubated in human serum or in C5-deficient AKR mouse serum reached the same levels, indicating that the amount of C5 present in serum during preincubation is not important for the degree of endocytosis. It is concluded that internalization of agarose by macrophages is mediated via the C3bi receptor.
我们已经确定了人单核细胞和小鼠腹腔巨噬细胞上产生琼脂糖结合的受体。通过使用分离的人补体因子C3、B和D,用C3b包被琼脂糖珠。在一些实验中,通过使用1:20稀释的人血清将C3b转化为C3bi。包被有C3b或C3bi的琼脂糖珠与单核细胞强烈结合。只有包被有C3bi的琼脂糖珠附着于小鼠巨噬细胞。用胰蛋白酶处理包被有C3bi的琼脂糖珠可消除其与巨噬细胞和单核细胞的附着,这可能是由于C3bi转化为C3d所致。在人血清或C5缺陷型AKR小鼠血清中预孵育的琼脂糖被巨噬细胞内吞的水平相同,这表明预孵育期间血清中C5的含量对于内吞程度并不重要。得出的结论是,巨噬细胞对琼脂糖的内化是通过C3bi受体介导的。