Chalapareddy S, Desai S A
Department of Biotechnology & Bioinformatics, School of Life Sciences, University of Hyderabad, Gachibowli, Telangana, India 500046.
Laboratory of Malaria and Vector Research, Division of Intramural Research, NIAID, National Institutes of Health, Rockville, MD, USA 20852.
Int J Curr Multidiscip Stud. 2017 Mar;3(3):619-623. Epub 2017 Mar 28.
Erythrocytes infected malaria parasites have increased permeability to nutrients and other solutes, as mediated by an unusual ion channel known as the plasmodial surface anion channel (PSAC). Although the increased permeability of infected erythrocytes was identified more than 70 years ago and subsequently characterized with tracer studies, its mechanism and role in parasite biology remained unclear until the introduction of patch-clamp methods and high-throughput screening technologies. These methods discovered and implicated PSAC as the primary mechanism, determined that this channel is essential for parasite development, led to identification of the channel's genes, and stimulated antimalarial drug discovery against this target. Despite these advances, many questions remain about this unusual parasite channel. Our review highlights some recent advances and describes important questions for future research.
感染疟原虫的红细胞对营养物质和其他溶质的通透性增加,这是由一种名为疟原虫表面阴离子通道(PSAC)的特殊离子通道介导的。尽管感染红细胞通透性增加在70多年前就已被发现,随后通过示踪研究进行了表征,但在膜片钳方法和高通量筛选技术出现之前,其机制及其在寄生虫生物学中的作用仍不清楚。这些方法发现并认为PSAC是主要机制,确定该通道对寄生虫发育至关重要,从而导致了该通道基因的鉴定,并推动了针对该靶点的抗疟药物研发。尽管取得了这些进展,但关于这个特殊的寄生虫通道仍有许多问题。我们的综述重点介绍了一些最新进展,并描述了未来研究的重要问题。