Webster R O, Rudofsky U H, Pickering R J
J Immunol. 1976 Sep;117(3):841-6.
Bone marrow transplants from normal Albany strain guinea pigs established a functional classical pathway of complement (C) in C4-deficient (C4D) guinea pigs. Seventeen days after transplant the Albany leads to C4D chimeras had detectable C4 and total hemolytic C activities. Maximum C4 levels (2 to 8% of normal were reachered by day 73 and restored total C to 40% of normal. Classical pathway function persisted for about 150 days and, thereafter, declined to undetectable levels by day 385. In contrast, Albany guinea pigs transplanted with C4D marrow maintained normal C4 levels throughout the experiment, suggesting that the C4-producing cells are radioresistant and long-lived. Unlike unmanipulated C4D animals, Albany leads to C4D chimeras were unable to produce antibodies to guinea pig C4 when immunized with normal guinea pig serum. These experiments suggest that bone marrow cell progeny produce C4 in vivo.
来自正常奥尔巴尼品系豚鼠的骨髓移植在C4缺陷(C4D)豚鼠中建立了补体(C)的功能性经典途径。移植后17天,接受奥尔巴尼豚鼠骨髓的C4D嵌合体具有可检测到的C4和总溶血C活性。到第73天时,C4水平达到最高(为正常水平的2%至8%),总补体恢复到正常水平的40%。经典途径功能持续约150天,此后,到第385天时降至检测不到的水平。相比之下,接受C4D骨髓移植的奥尔巴尼豚鼠在整个实验过程中C4水平保持正常,这表明产生C4的细胞具有放射抗性且寿命较长。与未处理的C4D动物不同,接受奥尔巴尼豚鼠骨髓的C4D嵌合体在用正常豚鼠血清免疫时无法产生针对豚鼠C4的抗体。这些实验表明骨髓细胞后代在体内产生C4。