Chromatin Dynamics and Genetic Variation Combine to Regulate Innate Immune Memory.

Journal of clinical & cellular immunology Pub Date : 2020-01-01 Epub Date: 2020-07-28
Jennifer Kim, Annie Vogel Ciernia
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Abstract

Recent work by Ciernia et al. (2020) identified how genetic and epigenetic mechanisms interact to regulate innate immune memory in bone marrow derived macrophages. The authors examined the BTBR strain, a naturally occurring mouse model of Autism Spectrum Disorder (ASD) that captures the complex genetics, behavioral and immune dysregulation found in the human disorder. Immune cell cultures from the BTBR strain compared to the standard C57 showed hyper-responsive immune gene expression that was linked to altered chromatin accessibility at sites with genetic differences between the strains. Together, findings from this work demonstrated that multiple levels of gene regulation likely dictate the formation of innate immune memory and are likely disrupted in immune cells in ASD. Future work will be needed to extend these findings to immune gene regulation in the brain and how changes in immune function are related to abnormal behaviors in brain disorders.

Abstract Image

染色质动力学和遗传变异共同调节先天免疫记忆。
Ciernia等人(2020)最近的工作确定了遗传和表观遗传机制如何相互作用以调节骨髓源性巨噬细胞的先天免疫记忆。作者研究了BTBR菌株,这是一种自然产生的自闭症谱系障碍(ASD)小鼠模型,它捕获了人类疾病中发现的复杂的遗传、行为和免疫失调。与标准C57相比,来自BTBR菌株的免疫细胞培养显示出高度反应性的免疫基因表达,这与菌株之间遗传差异位点的染色质可及性改变有关。总之,这项工作的发现表明,多个水平的基因调控可能决定了先天性免疫记忆的形成,并可能在ASD的免疫细胞中被破坏。未来的工作将需要将这些发现扩展到大脑中的免疫基因调节以及免疫功能的变化如何与大脑疾病中的异常行为相关。
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