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脲原体微小脲原体被宿主细胞自噬所困的细胞内命运。

Intracellular fate of Ureaplasma parvum entrapped by host cellular autophagy.

机构信息

Department of Developmental Medicine, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan.

Department of Bacteriology I, National Institute of Infectious Diseases, Tokyo, Japan.

出版信息

Microbiologyopen. 2017 Jun;6(3). doi: 10.1002/mbo3.441. Epub 2017 Jan 15.

Abstract

Genital mycoplasmas, including Ureaplasma spp., are among the smallest human pathogenic bacteria and are associated with preterm birth. Electron microscopic observation of U. parvum showed that these prokaryotes have a regular, spherical shape with a mean diameter of 146 nm. U. parvum was internalized into HeLa cells by clathrin-mediated endocytosis and survived for at least 14 days around the perinuclear region. Intracellular U. parvum reached endosomes in HeLa cells labeled with EEA1, Rab7, and LAMP-1 within 1 to 3 hr. After 3 hr of infection, U. parvum induced the cytosolic accumulation of galectin-3 and was subsequently entrapped by the autophagy marker LC3. However, when using atg7 MEF cells, autophagy was inadequate for the complete elimination of U. parvum in HeLa cells. U. parvum also colocalized with the recycling endosome marker Rab11. Furthermore, the exosomes purified from infected HeLa cell culture medium included U. parvum. In these purified exosomes ureaplasma lipoprotein multiple banded antigen, host cellular annexin A2, CD9, and CD63 were detected. This research has successfully shown that Ureaplasma spp. utilize the host cellular membrane compartments possibly to evade the host immune system.

摘要

生殖道支原体,包括脲原体属,是最小的人类病原体之一,与早产有关。电镜观察显示,这些原核生物呈规则的球形,平均直径为 146nm。微小脲原体通过网格蛋白介导的内吞作用被内化到 HeLa 细胞中,并在核周区域至少存活 14 天。在 HeLa 细胞中,内吞体在感染后 1 至 3 小时内被 EEAl、Rab7 和 LAMP-1 标记。感染 3 小时后,微小脲原体诱导 galectin-3 在细胞质中的积累,并随后被自噬标记物 LC3 捕获。然而,在使用 atg7 MEF 细胞时,自噬不足以完全清除 HeLa 细胞中的微小脲原体。微小脲原体还与再循环内体标记物 Rab11 共定位。此外,从感染的 HeLa 细胞培养物中纯化的外体中也检测到微小脲原体。在这些纯化的外体中检测到脲原体脂蛋白多带抗原、宿主细胞 annexin A2、CD9 和 CD63。这项研究成功地表明,脲原体属利用宿主细胞的膜区室,可能逃避宿主免疫系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/628a/5458467/4715ee836451/MBO3-6-na-g001.jpg

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