Silberstein Erica, Kim Kwang Sik, Acosta David, Debrabant Alain
Laboratory of Emerging Pathogens, Office of Blood Research and Review, Center for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, MD, United States.
Division of Pediatric Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Front Microbiol. 2021 Mar 4;12:626370. doi: 10.3389/fmicb.2021.626370. eCollection 2021.
(), the etiological agent of Chagas Disease (CD), is transmitted to humans by infected kissing bugs, blood transfusion, organ transplantation, and from mother-to-child. Congenital transmission is now considered an important route of CD spread in non-endemic countries where no routine testing of pregnant women for the disease is implemented. The main cellular mechanisms that lead to fetal infection by , despite the presence of a placental barrier, remain unclear. Mother-to-child transmission most likely occurs when bloodstream trypomastigotes reach the placental intervillous space and interact with the large cellular surface provided by the syncytioptrophoblasts. These highly specialized cells not only function as a physical obstacle between mother and fetus, but also modulate immune responses against pathogen infections. To overcome the limitations associated with the use of human fetal tissues, we employed a three-dimensional (3D) cell culture model to recreate the human placenta environment. In this system, the trophoblast-derived JEG-3 cell line is co-cultured with human brain microvascular endothelial cells attached to microcarrier beads in a rotating bioreactor. Here, we report that 3D culture of JEG-3/HBMEC spheroids promote JEG-3 cells differentiation revealed by the formation of syncytia and production of β human chorionic gonadotropin and human placental lactogen (hPL). Under these growth conditions, we demonstrate that 3D-grown JEG-3 cells have reduced susceptibility to infection compared to JEG-3 cells grown in conventional tissue culture flasks. We also show that 3D-cultured JEG-3 cells release paracrine factors in the supernatant that prevent infection of non-trophoblastic cell lines. Our model of vertical transmission may help better understand the molecular processes by which parasites bypass the human placental barrier and could be exploited to evaluate therapeutics to reduce congenital CD.
克氏锥虫( )是恰加斯病(CD)的病原体,可通过受感染的锥蝽、输血、器官移植以及母婴传播感染人类。在未对孕妇进行该疾病常规检测的非流行国家,先天性传播如今被视为恰加斯病传播的一条重要途径。尽管存在胎盘屏障,但导致胎儿被 感染的主要细胞机制仍不清楚。母婴传播最有可能发生在血流中的锥鞭毛体到达胎盘绒毛间隙并与合体滋养层细胞提供的大细胞表面相互作用时。这些高度特化的细胞不仅作为母体与胎儿之间的物理屏障发挥作用,还能调节针对病原体感染的免疫反应。为了克服使用人类胎儿组织的相关局限性,我们采用了三维(3D)细胞培养模型来重现人类胎盘环境。在这个系统中,滋养层来源的JEG - 3细胞系与附着在微载体珠上的人脑微血管内皮细胞在旋转生物反应器中共同培养。在此,我们报告JEG - 3/HBMEC球体的3D培养促进了JEG - 3细胞的分化,这通过合体细胞的形成以及β人绒毛膜促性腺激素和人胎盘催乳素(hPL)的产生得以体现。在这些生长条件下,我们证明与在传统组织培养瓶中生长的JEG - 3细胞相比,3D培养的JEG - 3细胞对 感染的易感性降低。我们还表明,3D培养的JEG - 3细胞在上清液中释放旁分泌因子,可防止非滋养层细胞系被 感染。我们的 垂直传播模型可能有助于更好地理解寄生虫绕过人类胎盘屏障的分子过程,并可用于评估减少先天性恰加斯病的治疗方法。