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一种干细胞策略确定血型糖蛋白C为啮齿动物疟原虫伯氏疟原虫的主要红细胞受体。

A Stem Cell Strategy Identifies Glycophorin C as a Major Erythrocyte Receptor for the Rodent Malaria Parasite Plasmodium berghei.

作者信息

Yiangou Loukia, Montandon Ruddy, Modrzynska Katarzyna, Rosen Barry, Bushell Wendy, Hale Christine, Billker Oliver, Rayner Julian C, Pance Alena

机构信息

Malaria Programme, Wellcome Trust Sanger Institute, Cambridge, United Kingdom.

Mouse Developmental Genetics and ES Cells Mutagenesis, Wellcome Trust Sanger Institute, Cambridge, United Kingdom.

出版信息

PLoS One. 2016 Jun 30;11(6):e0158238. doi: 10.1371/journal.pone.0158238. eCollection 2016.

Abstract

The clinical complications of malaria are caused by the parasite expansion in the blood. Invasion of erythrocytes is a complex process that depends on multiple receptor-ligand interactions. Identification of host receptors is paramount for fighting the disease as it could reveal new intervention targets, but the enucleated nature of erythrocytes makes genetic approaches impossible and many receptors remain unknown. Host-parasite interactions evolve rapidly and are therefore likely to be species-specific. As a results, understanding of invasion receptors outside the major human pathogen Plasmodium falciparum is very limited. Here we use mouse embryonic stem cells (mESCs) that can be genetically engineered and differentiated into erythrocytes to identify receptors for the rodent malaria parasite Plasmodium berghei. Two proteins previously implicated in human malaria infection: glycophorin C (GYPC) and Band-3 (Slc4a1) were deleted in mESCs to generate stable cell lines, which were differentiated towards erythropoiesis. In vitro infection assays revealed that while deletion of Band-3 has no effect, absence of GYPC results in a dramatic decrease in invasion, demonstrating the crucial role of this protein for P. berghei infection. This stem cell approach offers the possibility of targeting genes that may be essential and therefore difficult to disrupt in whole organisms and has the potential to be applied to a variety of parasites in diverse host cell types.

摘要

疟疾的临床并发症是由寄生虫在血液中的增殖引起的。红细胞入侵是一个复杂的过程,依赖于多种受体 - 配体相互作用。鉴定宿主受体对于抗击该疾病至关重要,因为这可能揭示新的干预靶点,但红细胞无细胞核的特性使得遗传方法无法实施,许多受体仍不为人知。宿主 - 寄生虫相互作用迅速演变,因此可能具有物种特异性。结果,对主要人类病原体恶性疟原虫之外的入侵受体的了解非常有限。在这里,我们使用可进行基因工程改造并分化为红细胞的小鼠胚胎干细胞(mESCs)来鉴定啮齿动物疟原虫伯氏疟原虫的受体。在mESCs中删除了先前与人类疟疾感染有关的两种蛋白质:血型糖蛋白C(GYPC)和带3蛋白(Slc4a1),以生成稳定的细胞系,这些细胞系朝着红细胞生成方向分化。体外感染试验表明,虽然删除带3蛋白没有影响,但缺乏GYPC会导致入侵显著减少,证明了该蛋白对伯氏疟原虫感染的关键作用。这种干细胞方法提供了靶向可能必不可少且因此在完整生物体中难以破坏的基因的可能性,并且有可能应用于多种宿主细胞类型中的各种寄生虫。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/902c/4928779/e06c9160dbc8/pone.0158238.g001.jpg

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