次级基因组在神经发育和协同进化动力学中的作用。

International review of neurobiology Pub Date : 2025-01-01 Epub Date: 2025-05-05 DOI:10.1016/bs.irn.2025.03.008
Siddharth Singh, Vaishali Saini, Hem Chandra Jha
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引用次数: 0

摘要

本章探讨了人类生物学和微生物“次级基因组”是如何通过肠脑轴共同进化来塑造神经发育的。微生物群落产生的代谢物穿过血脑和胎盘屏障,影响突触发生、免疫反应和神经回路形成。同时,人类加速区(HARs)和内源性逆转录病毒(ERVs)调节基因表达和免疫途径,决定哪些微生物在肠道中茁壮成长并影响大脑成熟。这些因素汇聚形成一个动态的宿主-微生物对话,对神经发育障碍(NDD)产生重大影响,包括自闭症谱系障碍(ASD)、注意力缺陷/多动障碍(ADHD)和精神分裂症。从进化的角度出发,本章阐述了遗传和免疫机制如何在早期大脑发育中协调有益的和病理的宿主-微生物相互作用。然后探索治疗策略,如益生菌、益生元、粪便微生物群移植和crispr驱动的微生物工程,针对肠道生态失调来减轻或预防神经发育障碍。此外,创新的器官芯片模型揭示了生理相关条件下的机制见解,在体外实验和临床应用之间提供了翻译桥梁。随着该领域的不断发展,这项工作强调了操纵微生物组以优化神经学结果的转化潜力。它丰富了我们对宿主基因组和微生物世界之间复杂的进化相互作用的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of secondary genomes in neurodevelopment and co-evolutionary dynamics.

This chapter examines how human biology and microbial "secondary genomes" have co-evolved to shape neurodevelopment through the gut-brain axis. Microbial communities generate metabolites that cross blood-brain and placental barriers, influencing synaptogenesis, immune responses, and neural circuit formation. Simultaneously, Human Accelerated Regions (HARs) and Endogenous Retroviruses (ERVs) modulate gene expression and immune pathways, determining which microbes thrive in the gut and impacting brain maturation. These factors converge to form a dynamic host-microbe dialogue with significant consequences for neurodevelopmental disorders (NDD), including autism spectrum disorder (ASD), attention-deficit/hyperactivity disorder (ADHD), and schizophrenia. Building on evolutionary perspectives, the chapter elucidates how genetic and immune mechanisms orchestrate beneficial and pathological host-microbe interactions in early brain development. It then explores therapeutic strategies, such as probiotics, prebiotics, fecal microbiota transplantation, and CRISPR-driven microbial engineering, targeting gut dysbiosis to mitigate or prevent neurodevelopmental dysfunctions. Furthermore, innovative organ-on-chip models reveal mechanistic insights under physiologically relevant conditions, offering a translational bridge between in vitro experiments and clinical applications. As the field continues to evolve, this work underscores the translational potential of manipulating the microbiome to optimize neurological outcomes. It enriches our understanding of the intricate evolutionary interplay between host genomes and the microbial world.

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