Physiological roles of embryonic microglia and their perturbation by maternal inflammation.

IF 4.2 3区 医学 Q2 NEUROSCIENCES
Frontiers in Cellular Neuroscience Pub Date : 2025-04-07 eCollection Date: 2025-01-01 DOI:10.3389/fncel.2025.1552241
Tsukasa Shimamura, Masashi Kitashiba, Kazutaka Nishizawa, Yuki Hattori
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Abstract

The interplay between the nervous and immune systems is well documented in the context of adult physiology and disease. Recent advances in understanding immune cell development have highlighted a significant interaction between neural lineage cells and microglia, the resident brain macrophages, during developmental stages. Throughout development, particularly from the embryonic to postnatal stages, diverse neural lineage cells are sequentially generated, undergo fate determination, migrate dynamically to their appropriate locations while maturing, and establish connections with their surroundings to form neural circuits. Previous studies have demonstrated that microglia contribute to this highly orchestrated process, ensuring the proper organization of brain structure. These findings underscore the need to further investigate how microglia behave and function within a broader framework of neurodevelopment. Importantly, recent epidemiological studies have suggested that maternal immune activation (MIA), triggered by various factors, such as viral or bacterial infections, environmental stressors, or other external influences, can affect neurogenesis and neural circuit formation, increasing the risk of neurodevelopmental disorders (NDDs) in offspring. Notably, many studies have revealed that fetal microglia undergo significant changes in response to MIA. Given their essential roles in neurogenesis and vascular development, inappropriate activation or disruption of microglial function may impair these critical processes, potentially leading to abnormal neurodevelopment. This review highlights recent advances in rodent models and human studies that have shed light on the behaviors and multifaceted roles of microglia during brain development, with a particular focus on the embryonic stage. Furthermore, drawing on insights from rodent MIA models, this review explores how MIA disrupts microglial function and how such disturbances may impair brain development, ultimately contributing to the onset of NDDs.

胚胎小胶质细胞的生理作用及其受母体炎症的干扰。
神经系统和免疫系统之间的相互作用在成人生理学和疾病的背景下得到了很好的记录。最近在理解免疫细胞发育方面的进展强调了神经谱系细胞和小胶质细胞(常驻脑巨噬细胞)在发育阶段之间的重要相互作用。在整个发育过程中,特别是从胚胎到出生后,不同的神经谱系细胞依次产生,经历命运的决定,在成熟过程中动态迁移到合适的位置,并与周围环境建立联系,形成神经回路。先前的研究表明,小胶质细胞参与了这一高度协调的过程,确保了大脑结构的适当组织。这些发现强调了进一步研究小胶质细胞如何在更广泛的神经发育框架内表现和功能的必要性。重要的是,最近的流行病学研究表明,由各种因素(如病毒或细菌感染、环境应激源或其他外部影响)触发的母体免疫激活(MIA)可影响神经发生和神经回路形成,增加后代神经发育障碍(ndd)的风险。值得注意的是,许多研究表明,胎儿小胶质细胞对MIA的反应发生了显著变化。鉴于它们在神经发生和血管发育中的重要作用,不适当的激活或破坏小胶质细胞功能可能会损害这些关键过程,潜在地导致神经发育异常。本文综述了啮齿动物模型和人类研究的最新进展,这些研究揭示了小胶质细胞在大脑发育过程中的行为和多方面作用,特别是在胚胎阶段。此外,根据啮齿动物MIA模型的见解,本综述探讨了MIA如何破坏小胶质细胞功能,以及这种干扰如何损害大脑发育,最终导致ndd的发生。
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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来源期刊
CiteScore
7.90
自引率
3.80%
发文量
627
审稿时长
6-12 weeks
期刊介绍: Frontiers in Cellular Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the cellular mechanisms underlying cell function in the nervous system across all species. Specialty Chief Editors Egidio D‘Angelo at the University of Pavia and Christian Hansel at the University of Chicago are supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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