Department of Microbiology and Cell Science, University of Florida, Building 981, Box 110700, Gainesville, FL 32669, USA.
Cell Microbiol. 2010 Oct;12(10):1480-94. doi: 10.1111/j.1462-5822.2010.01483.x.
Macrophages that express representative endoplasmic reticulum (ER) molecules tagged with green fluorescence protein were generated to assess the recruitment of ER molecules to Leishmania parasitophorous vacuoles (PVs). More than 90% of PVs harbouring Leishmania pifanoi or Leishmania donovani parasites recruited calnexin, to their PV membrane. An equivalent proportion of PVs also recruited the membrane-associated soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs), Sec22b. Both ER molecules appeared to be recruited very early in the formation of nascent PVs. Electron microscopy analysis of infected Sec22b/YFP expressing cells confirmed that Sec22b was recruited to Leishmania PVs. In contrast to PVs, it was found that no more than 20% of phagosomes that harboured Zymosan particles recruited calnexin or Sec22b to their limiting phagosomal membrane. The retrograde pathway that ricin employs to access the cell cytosol was exploited to gain further insight into ER-PV interactions. Ricin was delivered to PVs in infected cells incubated with ricin. Incubation of cells with brefeldin A blocked the transfer of ricin to PVs. This implied that molecules that traffic to the ER are transferred to PVs. Moreover the results show that PVs are hybrid compartments that are composed of both host ER and endocytic pathway components.
生成表达绿色荧光蛋白标记的代表性内质网 (ER) 分子的巨噬细胞,以评估 ER 分子向利什曼原虫寄生空泡 (PV) 的募集情况。超过 90%的含有利什曼原虫 pifanoi 或利什曼原虫 donovani 寄生虫的 PV 都募集了钙连蛋白到其 PV 膜上。相当比例的 PV 还募集了膜相关的可溶性 N-乙基马来酰亚胺敏感因子附着蛋白受体 (SNAREs),Sec22b。这两种 ER 分子似乎在新生 PV 的形成早期就被募集了。感染 Sec22b/YFP 表达细胞的电子显微镜分析证实,Sec22b 被募集到利什曼 PV 中。与 PV 不同的是,发现只有不超过 20%的含有 Zymosan 颗粒的吞噬体募集钙连蛋白或 Sec22b 到它们的限制吞噬体膜上。利用蓖麻毒素进入细胞胞质溶胶的逆行途径,进一步深入了解 ER-PV 相互作用。将蓖麻毒素递送到感染细胞中孵育的 PV 中。用布雷菲德菌素 A 孵育细胞会阻止蓖麻毒素向 PV 的转移。这意味着运输到 ER 的分子被转移到 PV 中。此外,研究结果表明,PV 是混合隔间,由宿主 ER 和内吞途径成分组成。
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