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分泌型阶段特异性糖蛋白4的碳水化合物部分参与细胞外无鞭毛体对宿主细胞的侵袭。

A Carbohydrate Moiety of Secreted Stage-Specific Glycoprotein 4 Participates in Host Cell Invasion by Extracellular Amastigotes.

作者信息

Florentino Pilar T V, Real Fernando, Orikaza Cristina M, da Cunha Julia P C, Vitorino Francisca N L, Cordero Esteban M, Sobreira Tiago J P, Mortara Renato A

机构信息

Department of Microbiology, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, Brazil.

Institut Cochin, INSERM U1016, Paris, France.

出版信息

Front Microbiol. 2018 Apr 10;9:693. doi: 10.3389/fmicb.2018.00693. eCollection 2018.

Abstract

is the etiologic agent of Chagas' disease. It is known that amastigotes derived from trypomastigotes in the extracellular milieu are infective and . Extracellular amastigotes (EAs) have a stage-specific surface antigen called Ssp-4, a GPI-anchored glycoprotein that is secreted by the parasites. By immunoprecipitation with the Ssp-4-specific monoclonal antibodies (mAb) 2C2 and 1D9, we isolated the glycoprotein from EAs. By mass spectrometry, we identified the core protein of Ssp-4 and evaluated mRNA expression and the presence of Ssp-4 carbohydrate epitopes recognized by mAb1D9. We demonstrated that the carbohydrate epitope recognized by mAb1D9 could promote host cell invasion by EAs. Although infectious EAs express lower amounts of Ssp-4 compared with less-infectious EAs (at the mRNA and protein levels), it is the glycosylation of Ssp-4 (identified by mAb1D9 staining only in infectious strains and recognized by galectin-3 on host cells) that is the determinant of EA invasion of host cells. Furthermore, Ssp-4 is secreted by EAs, either free or associated with parasite vesicles, and can participate in host-cell interactions. The results presented here describe the possible role of a carbohydrate moiety of surface glycoproteins in host cell invasion by EA forms, highlighting the potential of these moieties as therapeutic and vaccine targets for the treatment of Chagas' disease.

摘要

是恰加斯病的病原体。已知在细胞外环境中源自锥鞭毛体的无鞭毛体具有感染性。细胞外无鞭毛体(EA)有一种阶段特异性表面抗原,称为Ssp-4,这是一种由寄生虫分泌的糖基磷脂酰肌醇锚定糖蛋白。通过用Ssp-4特异性单克隆抗体(mAb)2C2和1D9进行免疫沉淀,我们从EA中分离出了这种糖蛋白。通过质谱分析,我们鉴定了Ssp-4的核心蛋白,并评估了mRNA表达以及mAb1D9识别的Ssp-4碳水化合物表位的存在情况。我们证明,mAb1D9识别的碳水化合物表位可促进EA对宿主细胞的侵袭。尽管与感染性较低的EA相比,感染性EA在mRNA和蛋白质水平上表达的Ssp-4量较低,但Ssp-4的糖基化(仅在感染性菌株中通过mAb1D9染色鉴定,并被宿主细胞上的半乳糖凝集素-3识别)才是EA侵袭宿主细胞的决定因素。此外,Ssp-4由EA分泌,可游离存在或与寄生虫囊泡相关,并可参与宿主细胞相互作用。此处呈现的结果描述了表面糖蛋白的碳水化合物部分在EA形式侵袭宿主细胞中的可能作用,突出了这些部分作为治疗恰加斯病的治疗靶点和疫苗靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a478/5903068/ea7b73575d08/fmicb-09-00693-g001.jpg

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