Garcia-del Portillo F, Zwick M B, Leung K Y, Finlay B B
Biotechnology Laboratory, University of British Columbia, Vancouver, Canada.
Infect Agents Dis. 1993 Aug;2(4):227-31.
We have examined the targeting of S. typhimurium-containing vacuoles to lysosomes after invasion of cultured HeLa epithelial cells. Our results show that intracellular bacteria colocalize with vacuoles containing lysosomal membrane glycoproteins (LGPs). Both human LGPs, hlamp-1 and hlamp-2, are present in S. typhimurium-containing vacuoles from approximately 2 h postinfection. At later times (4-6 h), long and stable filamentous structures with lysosomal markers appear connected to bacteria-containing vacuoles in infected cells. Viable intracellular bacteria are required for the formation of these structures, which are not detected in uninfected cells or in HeLa epithelial cells infected with another invasive bacteria, Yersinia enterocolitica. Kinetics analysis showed a strict correlation between the appearance of these LGP-rich filaments and the initiation of intracellular bacterial replication. Moreover, these structures are absent in epithelial cells infected with certain S. typhimurium intracellular replication-defective mutants. Additional data confirmed that an intact microtubule network and intravacuolar acidic pH are required to induce the formation of LGP-containing filamentous structures and that these structures are morphologically and functionally different from previously described tubular lysosomes.
我们研究了鼠伤寒沙门氏菌侵入培养的HeLa上皮细胞后,含沙门氏菌液泡靶向溶酶体的情况。我们的结果表明,细胞内细菌与含有溶酶体膜糖蛋白(LGP)的液泡共定位。人LGP,即hlamp - 1和hlamp - 2,在感染后约2小时就存在于含鼠伤寒沙门氏菌的液泡中。在稍后的时间(4 - 6小时),带有溶酶体标记物的长而稳定的丝状结构出现在感染细胞中与含细菌液泡相连的位置。这些结构的形成需要活的细胞内细菌,在未感染细胞或感染另一种侵袭性细菌——小肠结肠炎耶尔森氏菌的HeLa上皮细胞中未检测到这些结构。动力学分析表明,这些富含LGP的细丝的出现与细胞内细菌复制的起始之间存在严格的相关性。此外,在感染某些鼠伤寒沙门氏菌细胞内复制缺陷突变体的上皮细胞中不存在这些结构。其他数据证实,完整的微管网络和液泡内酸性pH是诱导含LGP丝状结构形成所必需的,并且这些结构在形态和功能上与先前描述的管状溶酶体不同。