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Maternal immune activation causes age- and region-specific changes in brain cytokines in offspring throughout development

机译:母体免疫激活导致在整个发育中后代脑细胞因子的年龄和区域特异性变化

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摘要

Maternal infection is a risk factor for autism spectrum disorder (ASD) and schizophrenia (SZ). Indeed, modeling this risk factor in mice through maternal immune activation (MIA) causes ASD- and SZ-like neuropathologies and behaviors in the offspring. Although MIA upregulates pro-inflammatory cytokines in the fetal brain, whether MIA leads to long-lasting changes in brain cytokines during postnatal development remains unknown. Here, we tested this possibility by measuring protein levels of 23 cytokines in the blood and three brain regions from offspring of poly(I:C)- and saline-injected mice at five postnatal ages using multiplex arrays. Most cytokines examined are present in sera and brains throughout development. MIA induces changes in the levels of many cytokines in the brains and sera of offspring in a region- and age-specific manner. These MIA-induced changes follow a few, unexpected and distinct patterns. In frontal and cingulate cortices, several, mostly pro-inflammatory, cytokines are elevated at birth, followed by decreases during periods of synaptogenesis and plasticity, and increases again in the adult. Cytokines are also altered in postnatal hippocampus, but in a pattern distinct from the other regions. The MIA-induced changes in brain cytokines do not correlate with changes in serum cytokines from the same animals. Finally, these MIA-induced cytokine changes are not accompanied by breaches in the blood-brain barrier, immune cell infiltration or increases in microglial density. Together, these data indicate that MIA leads to long-lasting, region-specific changes in brain cytokines in offspring—similar to those reported for ASD and SZ—that may alter CNS development and behavior.
机译:产妇感染是自闭症谱系障碍(ASD)和精神分裂症(SZ)的危险因素。实际上,通过母体免疫激活(MIA)在小鼠中模拟这种危险因素会导致后代出现ASD和SZ样的神经病理和行为。尽管MIA会上调胎儿大脑中的促炎性细胞因子,但MIA是否会导致出生后发育过程中脑细胞因子的长期变化仍然未知。在这里,我们通过使用多重阵列测量了五个出生后年龄的,注射了聚(I:C)和生理盐水的小鼠后代的血液和三个大脑区域的23种细胞因子的蛋白质水平,测试了这种可能性。在整个发育过程中,大多数检查的细胞因子都存在于血清和大脑中。 MIA以区域和年龄特定的方式诱导后代的大脑和血清中许多细胞因子水平的改变。这些由MIA引起的变化遵循一些意外的独特模式。在额叶和扣带状皮层中,几种在出生时升高的细胞因子(大多数为促炎性细胞因子)升高,随后在突触形成和可塑性时期降低,并在成年人中再次升高。产后海马中的细胞因子也发生改变,但是其模式不同于其他区域。 MIA诱导的脑细胞因子变化与来自相同动物的血清细胞因子变化不相关。最后,这些MIA诱导的细胞因子变化不会伴随血脑屏障的破坏,免疫细胞的浸润或小胶质细胞密度的增加。总之,这些数据表明,MIA导致后代中脑细胞因子的长期特定区域变化,这与ASD和SZ报道的相似,可能会改变CNS的发育和行为。

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