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病原体激活的母体 T 细胞拯救母源免疫激活诱导的成年小鼠后代的行为异常。

Rescue of maternal immune activation-induced behavioral abnormalities in adult mouse offspring by pathogen-activated maternal T cells.

机构信息

State Key Laboratory of Reproductive Medicine, Department of Pathogen Biology, Jiangsu Province Key Laboratory of Modern Pathogen Biology, Nanjing Medical University, Nanjing, China.

Shanghai Key Laboratory of Psychotic Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Nat Neurosci. 2021 Jun;24(6):818-830. doi: 10.1038/s41593-021-00837-1. Epub 2021 Apr 15.

Abstract

Maternal immune activation (MIA) induced by lipopolysaccharides or polyinosinic:polycytidylic acid injections can induce behavioral abnormalities in adult mouse offspring. Here, we used the soluble tachyzoite antigen from Toxoplasma gondii, a parasite that infects approximately two billion people, to induce MIA in mice. The adult male offspring showed autism-relevant behaviors and abnormal brain microstructure, along with a pro-inflammatory T-cell immune profile in the periphery and upregulation of interleukin-6 in brain astrocytes. We show that adoptive transfer of regulatory T (T) cells largely reversed these MIA-induced phenotypes. Notably, pathogen-activated maternal T cells showed greater rescue efficacy than those from control donors. Single-cell RNA sequencing identified and characterized a unique group of pathogen-activated T cells that constitute 32.6% of the pathogen-activated maternal T population. Our study establishes a new preclinical parasite-mimicking MIA model and suggests therapeutic potential of adoptive T cell transfer in neuropsychiatric disorders associated with immune alterations.

摘要

母体免疫激活(MIA)由脂多糖或聚肌苷酸:聚胞苷酸注射诱导,可诱导成年小鼠后代出现行为异常。在这里,我们使用寄生虫刚地弓形虫的可溶性速殖子抗原来诱导小鼠的 MIA。成年雄性后代表现出自闭症相关的行为和异常的大脑微观结构,以及外周炎症性 T 细胞免疫特征和大脑星形胶质细胞中白细胞介素-6 的上调。我们表明,调节性 T(T)细胞的过继转移在很大程度上逆转了这些 MIA 诱导的表型。值得注意的是,病原体激活的母体 T 细胞比对照供体的细胞具有更高的拯救效果。单细胞 RNA 测序鉴定并表征了一组独特的病原体激活 T 细胞,它们构成了病原体激活的母体 T 细胞群体的 32.6%。我们的研究建立了一种新的寄生虫模拟的 MIA 模型,并表明过继性 T 细胞转移在与免疫改变相关的神经精神疾病中的治疗潜力。

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