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首页> 外文期刊>Parasitology International >Intravital microscopy technique to study parasite dynamics in the labyrinth layer of the mouse placenta. (Special Section: In vivo imaging of parasite infection.)
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Intravital microscopy technique to study parasite dynamics in the labyrinth layer of the mouse placenta. (Special Section: In vivo imaging of parasite infection.)

机译:活体显微镜技术研究小鼠胎盘迷宫层中的寄生虫动力学。 (特别部分:寄生虫感染的体内成像。)

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摘要

Intravital imaging techniques are the best approach to investigate in situ cellular behavior under physiological conditions. Many techniques have emerged during these last few years for this purpose. We recently described an intravital imaging technique that allows for the observation of placenta physiological responses at the labyrinth layer of this tissue. This technique will be very useful to study many placental opportunistic infections and in this article we reinforce its usefulness by analyzing placental physiological entrapment of beads and parasites. In particular, our results show that small beads (1.0 micro m) or Plasmodium chabaudi-GFP-infected-Red Blood Cells (Pc-GFP-iRBCs) cannot get trapped inside small or large blood vessels of popliteal lymph nodes (PLNs). Inside the placenta, clusters of beads could only be found inside the maternal blood vessels. However, Pc-GFP-iRBCs were found inside and outside the maternal blood vessels. We observed that trophoblasts can ingest infected-Red Blood Cells (iRBCs) in vitro and immunofluorescence of placenta revealed Pc-GFP-iRBCs inside and outside the maternal blood vessels. Taken together, we conclude that fast deposition of particles inside blood vessels seems to be an intrinsic characteristic of placenta blood flow, but iRBCs could be internalized by trophoblast cells. Thus these results represent one of the many possible uses of our intravital imaging technique to address important questions inside the parasitological field.
机译:活体成像技术是研究生理条件下原位细胞行为的最佳方法。在最近几年中,为此目的出现了许多技术。我们最近描述了一种活体成像技术,可以观察该组织的迷宫层的胎盘生理反应。该技术对于研究许多胎盘机会性感染将非常有用,在本文中,我们将通过分析胎盘的珠粒和寄生虫的生理滞留来增强其用途。特别是,我们的研究结果表明,小珠(1.0微米)或沙巴氏梭状芽孢杆菌-GFP感染的红细胞(Pc-GFP-iRBCs)不能被困在pop淋巴结(PLNs)的大或小血管内。在胎盘内部,只能在母体血管内部发现珠簇。然而,Pc-GFP-iRBCs被发现在产妇血管内外。我们观察到,滋养层细胞可以在体外摄入被感染的红细胞(iRBCs),胎盘的免疫荧光检测显示母体血管内外的Pc-GFP-iRBCs。两者合计,我们得出结论,颗粒在血管内的快速沉积似乎是胎盘血流的固有特征,但iRBCs可能被滋养细胞所内化。因此,这些结果代表了我们的活体成像技术解决寄生虫学领域内重要问题的众多可能用途之一。

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