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人类血管内寄生吸虫曼氏血吸虫的核黄素(维生素B2)转运蛋白(SmaRT)

The riboflavin (vitamin B2) transporter protein (SmaRT) of the human intravascular parasitic trematode Schistosoma mansoni.

作者信息

Da'dara Akram A, Gondane Roshni, Skelly Patrick J

机构信息

Molecular Helminthology Laboratory, Department of Infectious Disease and Global Health, Cummings School of Veterinary Medicine, Tufts University, North Grafton, MA, USA.

出版信息

Heliyon. 2024 Mar 22;10(7):e28271. doi: 10.1016/j.heliyon.2024.e28271. eCollection 2024 Apr 15.

Abstract

Schistosomes are intravascular parasitic worms infecting >200 million people globally. Here we examine how the worms acquire an essential nutrient - vitamin B2 (riboflavin). We demonstrate that all intravascular life stages (schistosomula, adult males and females) take up radiolabeled riboflavin. This process is impeded in the presence of excess unlabeled riboflavin and at 4 °C. We have identified a transporter homolog in worms designated SmaRT ( riboflavin transporter) that localizes to the tegument and internal tissues of adults. CHO-S cells transfected with plasmid encoding SmaRT import significantly more radiolabeled riboflavin compared to controls. Uptake of radiolabel is impeded when SmaRT-expressing cells are incubated in an excess of unlabeled riboflavin but not by an excess of an irrelevant metabolite. Uptake is mediated in a sodium-independent manner and over a wide range of pH values (pH 5.5-9). This is the first identification of a riboflavin transporter in any platyhelminth.

摘要

血吸虫是一种血管内寄生蠕虫,全球感染人数超过2亿。在这里,我们研究了这些蠕虫如何获取一种必需营养素——维生素B2(核黄素)。我们证明,所有血管内生命阶段(童虫、成年雄虫和雌虫)都能摄取放射性标记的核黄素。在存在过量未标记核黄素的情况下以及在4°C时,这个过程会受到阻碍。我们在蠕虫中鉴定出一种转运蛋白同源物,命名为SmaRT(核黄素转运蛋白),它定位于成虫的体表和内部组织。与对照相比,用编码SmaRT的质粒转染的CHO-S细胞摄取的放射性标记核黄素明显更多。当将表达SmaRT的细胞与过量未标记核黄素一起孵育时,放射性标记物的摄取会受到阻碍,但过量的无关代谢物则不会产生这种影响。摄取是以不依赖钠的方式进行的,并且在很宽的pH值范围(pH 5.5 - 9)内都能发生。这是在任何扁形动物中首次鉴定出核黄素转运蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3107/11004526/b6742dcfb0ae/gr1.jpg

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