Toxoplasma gondii infection misdirects placental trophoblast lineage specification

Leah F. Cabo, Liheng Yang, Mingze Gao, Rafaela J. da Silva, NyJaee N. Washington, Sarah M. Reilly, Christina J. Megli, Carolyn B. Coyne, Jon P. Boyle
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Abstract

Pregnancy is a critical point of vulnerability to infection and other insults that could compromise proper fetal development. The placenta acts as a protective and nutrient-permeable barrier to most infectious agents, but a few are capable of bypassing its defenses. Remarkably little is known about how exposure to these select pathogens might impact ongoing placental development. Here we demonstrate that Toxoplasma gondii entirely misdirects the developmental program of trophoblast stem cells. Infection of progenitor cytotrophoblasts prevents fusion and differentiation to infection-resistant syncytiotrophoblast. Rather, T. gondii elicits a unique transcriptional identity that polarizes cytotrophoblasts to the infection-permissive extravillous trophoblast fate. Strong evidence of developmental disruption is found in multiple orthogonal models, including trophoblast stem cells, trophoblast organoids, and chorionic villi. Manipulation of cell fate by the parasite is most dramatic in trophoblast organoids, where we see robust outgrowth of HLA-G(+) extravillous trophoblasts. Collectively, these data show that Toxoplasma antagonizes differentiation of an infection-resistant cell type by inducing formation of an infection-permissive cell type, therefore potentiating its own transmission to the fetus.
弓形虫感染会误导胎盘滋养层细胞系的分化
妊娠期是胎儿容易受到感染和其他损伤的关键时期,这些损伤可能会影响胎儿的正常发育。胎盘对大多数感染性病原体起着保护和营养渗透屏障的作用,但也有少数病原体能够绕过胎盘的防御。对于接触这些特定病原体会如何影响胎盘的持续发育,人们知之甚少。在这里,我们证明弓形虫会完全误导滋养层干细胞的发育程序。原代滋养细胞受到感染后会阻止融合和分化为抗感染的合胞滋养细胞。相反,淋球菌会引起一种独特的转录特性,将滋养细胞极化为允许感染的滋养外细胞。在滋养层干细胞、滋养层有机体和绒毛等多个正交模型中都发现了发育中断的有力证据。寄生虫对细胞命运的操纵在滋养层有机体中最为显著,我们在其中看到了HLA-G(+)外滋养层滋养细胞的强劲生长。总之,这些数据表明弓形虫通过诱导形成允许感染的细胞类型来拮抗抗感染细胞类型的分化,从而增强其自身向胎儿的传播。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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