Silva Valeria Oliveira, Maia Marta Marques, Torrecilhas Ana Claudia, Taniwaki Noemi Nosomi, Namiyama Gislene Mitsue, Oliveira Katia Cristina, Ribeiro Kleber Silva, Toledo Maytê Dos Santos, Xander Patricia, Pereira-Chioccola Vera Lucia
Laboratório de Biologia Molecular de Parasitas e Fungos, Instituto Adolfo Lutz, Sao Paulo, Brazil.
Departamento de Ciências Farmacêuticas, Campus Diadema, Universidade Federal de Sao Paulo, Sao Paulo, Brazil.
Parasite Immunol. 2018 Sep;40(9):e12571. doi: 10.1111/pim.12571. Epub 2018 Aug 1.
This study established a protocol to purify Toxoplasma gondii tachyzoite microvesicles and exosomes, called as extracellular vesicles (EVs). In addition, the investigations were conducted to determine the kinetic of EV release by tachyzoites and whether EV proteins are able to modulate the host immune response. The particle size and concentration released by tachyzoites in culture medium at different incubation-period were characterized by nanoparticle tracking analysis. Tachyzoites (1 × 10 ) released around 4.37 ± 0.81 × 10 EVs/mL/h, with size varying between 138.2 and 171.9 nm. EVs released into the medium were purified by gel-exclusion chromatography and screened by ELISA, using a pool of human positive sera for toxoplasmosis. EV-fractions contained high concentration of proteins, and EVs were analyzed by scanning and transmission electron microscopies. Tachyzoites released EVs into the culture medium throughout all membrane surface, and these vesicles contain small RNAs/miRNA. Pooled sera from chronically infected human or mice (infected with 2 different T. gondii strains) recognized distinct EV electrophoretic patterns in immunoblotting. T. gondii EVs significantly induced IL-10, TNF-α and iNOS in murine macrophages. In conclusion, this study shows that T. gondii secrete/excrete EVs (microvesicles and exosomes) contain miRNA and they were immunologically recognized by host immune response.
本研究建立了一种纯化刚地弓形虫速殖子微囊泡和外泌体(称为细胞外囊泡,EVs)的方案。此外,还进行了相关研究以确定速殖子释放EVs的动力学,以及EVs蛋白是否能够调节宿主免疫反应。通过纳米颗粒跟踪分析对不同孵育期的速殖子在培养基中释放的颗粒大小和浓度进行了表征。速殖子(1×10 )每小时每毫升释放约4.37±0.81×10 个EVs,大小在138.2至171.9纳米之间变化。释放到培养基中的EVs通过凝胶排阻色谱法进行纯化,并使用一组人类弓形虫病阳性血清通过ELISA进行筛选。EVs组分含有高浓度蛋白质,通过扫描电子显微镜和透射电子显微镜对EVs进行分析。速殖子通过其整个膜表面将EVs释放到培养基中,并且这些囊泡含有小RNA/miRNA。来自慢性感染人类或小鼠(感染2种不同刚地弓形虫株)的混合血清在免疫印迹中识别出不同的EV电泳图谱。刚地弓形虫EVs显著诱导小鼠巨噬细胞中的IL-10、TNF-α和iNOS。总之,本研究表明刚地弓形虫分泌/排泄的EVs(微囊泡和外泌体)含有miRNA,并且它们能被宿主免疫反应进行免疫识别。