Little J S, Kishimoto R A, Canonico P G
J Reticuloendothel Soc. 1983 May;33(5):331-41.
Cultivated guinea pig peritoneal macrophages were infected with radio-labeled phase I Coxiella burnetii in order to assess the intracellular distribution of ingested rickettsiae. Localization of organisms was determined by fractionation of macrophage homogenates by equilibrium density centrifugation on sucrose gradients. Macrophages isolated from either nonimmune or immune guinea pigs and infected with C burnetii opsonized with immune serum yielded equilibrium density distribution for rickettsiae similar to lysosomal enzymes, suggesting sequestration within macrophage lysosomes. To confirm these observations nonimmune or immune guinea pigs were injected with Triton WR-1339 prior to macrophage harvest to decrease the density of macrophage lysosomes. Triton-laden macrophages infected with opsonized rickettsiae resulted in equilibrium density distribution for lysosomal enzymes and organisms in less dense regions of the gradient. In contrast, when either nonimmune or immune macrophages were infected in the presence of normal guinea pig serum, the distribution of labeled rickettsiae in the gradient did not correspond with lysosomes. We conclude that in the absence of immune serum, ingested C burnetii are not sequestered within macrophage lysosomes. Phagolysomal fusion and subsequent degradation of rickettsiae within the lysosomes of the macrophages appear to occur only when C burnetii are opsonized with immune serum.
为了评估摄入的立克次体在细胞内的分布情况,用放射性标记的Ⅰ期伯纳特柯克斯体感染培养的豚鼠腹腔巨噬细胞。通过在蔗糖梯度上进行平衡密度离心对巨噬细胞匀浆进行分级分离,来确定微生物的定位。从非免疫或免疫豚鼠中分离出的巨噬细胞,用免疫血清调理过的伯纳特柯克斯体感染后,立克次体的平衡密度分布与溶酶体酶相似,表明其被隔离在巨噬细胞溶酶体内。为了证实这些观察结果,在收获巨噬细胞之前,给非免疫或免疫豚鼠注射曲拉通WR-1339,以降低巨噬细胞溶酶体的密度。用调理过的立克次体感染含曲拉通的巨噬细胞,导致溶酶体酶和微生物在梯度密度较低区域的平衡密度分布。相反,当在正常豚鼠血清存在的情况下感染非免疫或免疫巨噬细胞时,梯度中标记立克次体的分布与溶酶体不对应。我们得出结论,在没有免疫血清的情况下,摄入的伯纳特柯克斯体不会被隔离在巨噬细胞溶酶体内。只有当伯纳特柯克斯体用免疫血清调理时,巨噬细胞溶酶体内才会发生吞噬溶酶体融合以及随后立克次体的降解。