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发育应激源诱导小胶质细胞固有免疫记忆,并导致疾病风险。

Developmental Stressors Induce Innate Immune Memory in Microglia and Contribute to Disease Risk.

机构信息

Department of Molecular and Cellular Biology, Dartmouth College, Hanover, NH 03755, USA.

Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Int J Mol Sci. 2021 Dec 2;22(23):13035. doi: 10.3390/ijms222313035.

Abstract

Many types of stressors have an impact on brain development, function, and disease susceptibility including immune stressors, psychosocial stressors, and exposure to drugs of abuse. We propose that these diverse developmental stressors may utilize a common mechanism that underlies impaired cognitive function and neurodevelopmental disorders such as schizophrenia, autism, and mood disorders that can develop in later life as a result of developmental stressors. While these stressors are directed at critical developmental windows, their impacts are long-lasting. Immune activation is a shared pathophysiology across several different developmental stressors and may thus be a targetable treatment to mitigate the later behavioral deficits. In this review, we explore different types of prenatal and perinatal stressors and their contribution to disease risk and underlying molecular mechanisms. We highlight the impact of developmental stressors on microglia biology because of their early infiltration into the brain, their critical role in brain development and function, and their long-lived status in the brain throughout life. Furthermore, we introduce innate immune memory as a potential underlying mechanism for developmental stressors' impact on disease. Finally, we highlight the molecular and epigenetic reprogramming that is known to underlie innate immune memory and explain how similar molecular mechanisms may be at work for cells to retain a long-term perturbation after exposure to developmental stressors.

摘要

许多类型的应激源都会对大脑发育、功能和疾病易感性产生影响,包括免疫应激源、心理社会应激源和滥用药物。我们提出,这些不同的发育应激源可能利用一种共同的机制,这种机制是导致认知功能障碍和神经发育障碍(如精神分裂症、自闭症和情绪障碍)的基础,这些障碍可能在发育应激源之后的生命中发展。虽然这些应激源针对的是关键的发育窗口期,但它们的影响是持久的。免疫激活是几种不同发育应激源的共同病理生理学,因此可能是一种可靶向的治疗方法,以减轻后期的行为缺陷。在这篇综述中,我们探讨了不同类型的产前和围产期应激源及其对疾病风险和潜在分子机制的贡献。我们强调了发育应激源对小胶质细胞生物学的影响,因为它们早期浸润大脑,在大脑发育和功能中起着关键作用,并且在整个生命过程中在大脑中保持长期存在。此外,我们介绍了先天免疫记忆作为发育应激源对疾病影响的潜在潜在机制。最后,我们强调了已知是先天免疫记忆基础的分子和表观遗传重编程,并解释了在暴露于发育应激源后,细胞如何保持长期的扰动,可能存在相似的分子机制。

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