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内吞 SNARE 参与了最佳状态下的柯克斯体囊泡的发育。

Endocytic SNAREs are involved in optimal Coxiella burnetii vacuole development.

机构信息

Laboratorio de Biología Celular y Molecular- Instituto de Histología y Embriología IHEM, Facultad de Ciencias Médicas, Universidad Nacional de Cuyo-CONICET, Mendoza, Argentina.

出版信息

Cell Microbiol. 2013 Jun;15(6):922-41. doi: 10.1111/cmi.12087. Epub 2013 Jan 7.

Abstract

Coxiella burnetii is a Gram-negative intracellular bacterium. As previously described, both the endocytic and the autophagic pathways contribute to the maturation of Coxiella replicative vacuoles (CRVs). The large CRVs share the properties of both phagolysosomal and autophagolysosomal compartments. Vamp3, Vamp7 and Vamp8 are v-SNAREs involved in the endocytic pathway which participate mainly in the fusion between endosomes and lysosomes. In the present study we observed that Vamp7 interacts with C. burnetii at different infection times (1 h-48 h p.i.). We have determined that a truncated mutant of Vamp7 (Vamp7 NT) and a siRNA against this SNARE protein affects the optimal development of CRVs, suggesting that Vamp7 mediates fusion events that are required for the biogenesis of CRVs. Indeed, we have observed that overexpression of Vamp7 NT inhibited the heterotypic fusion with lysosomes and the homotypic fusion between individual Coxiella phagosomes and CRVs. Moreover, we have detected in the vacuole membrane, at different infection times, the Vamp7 partners (Vti1a and Vti1b). Interestingly, treatment with chloramphenicol reduced the colocalization between C. burnetii and Vamp7, Vti1a or Vti1b, indicating that the recruitment of these SNAREs proteins is a bacteria-driven process that favours the CRV biogenesis, likely by facilitating the interaction with the endolysosomal compartment.

摘要

贝氏考克斯体是一种革兰氏阴性的细胞内细菌。如前所述,内吞作用和自噬途径都有助于考克斯氏体复制空泡(CRV)的成熟。大型 CRV 具有吞噬溶酶体和自噬溶酶体两者的特性。Vamp3、Vamp7 和 Vamp8 是参与内吞作用途径的 v-SNAREs,主要参与内体与溶酶体之间的融合。在本研究中,我们观察到 Vamp7 在不同的感染时间(1 h-48 h p.i.)与 C. burnetii 相互作用。我们已经确定 Vamp7 的截断突变体(Vamp7 NT)和针对该 SNARE 蛋白的 siRNA 会影响 CRV 的最佳发育,这表明 Vamp7 介导了对于 CRV 生物发生所需的融合事件。事实上,我们已经观察到 Vamp7 NT 的过表达抑制了与溶酶体的异型融合以及 Coxiella 吞噬体与 CRV 之间的同源融合。此外,我们在不同的感染时间检测到了 vacuole 膜上的 Vamp7 伴侣(Vti1a 和 Vti1b)。有趣的是,氯霉素处理降低了 C. burnetii 与 Vamp7、Vti1a 或 Vti1b 之间的共定位,表明这些 SNARE 蛋白的募集是一个由细菌驱动的过程,这有利于 CRV 的生物发生,可能通过促进与内溶酶体 compartment 的相互作用来实现。

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