妊娠早期的母亲饮食会影响小胶质细胞对产后味觉活动的依赖性修剪。

IF 12.6 1区 医学 Q1 IMMUNOLOGY Journal of Experimental Medicine Pub Date : 2023-12-04 Epub Date: 2023-09-21 DOI:10.1084/jem.20212476
Chengsan Sun, Shuqiu Zheng, Justin S A Perry, Geoffrey T Norris, Mei Cheng, Fanzhen Kong, Rolf Skyberg, Jianhua Cang, Alev Erisir, Jonathan Kipnis, David L Hill
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摘要

中枢感觉回路发育的一个关键过程涉及对旺盛末梢的活动依赖性修剪。在这里,我们研究了出生后小鼠孤束核(NST)在正常发育过程中的味觉终末场成熟,以及在怀孕后不久给母亲喂食低NaCl饮食的小鼠中。对照组味觉神经末梢区的修剪涉及补体系统,可能是由NaCl引发的味觉活动驱动的。相比之下,早期饮食控制的母亲的后代即使外围味觉活动发育正常,也无法修剪味觉末端区域。这些小鼠的修剪能力是通过在出生后激活骨髓细胞来拯救的,相反,在骨髓细胞功能丧失的对照组中,修剪被阻止。修剪和骨髓细胞功能的改变似乎是在外周味觉系统组装之前编程的,对应于从卵黄囊衍生的小胶质细胞祖细胞迁移到大脑并定植于大脑的胚胎期。
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Maternal diet during early gestation influences postnatal taste activity-dependent pruning by microglia.

A key process in central sensory circuit development involves activity-dependent pruning of exuberant terminals. Here, we studied gustatory terminal field maturation in the postnatal mouse nucleus of the solitary tract (NST) during normal development and in mice where their mothers were fed a low NaCl diet for a limited period soon after conception. Pruning of terminal fields of gustatory nerves in controls involved the complement system and is likely driven by NaCl-elicited taste activity. In contrast, offspring of mothers with an early dietary manipulation failed to prune gustatory terminal fields even though peripheral taste activity developed normally. The ability to prune in these mice was rescued by activating myeloid cells postnatally, and conversely, pruning was arrested in controls with the loss of myeloid cell function. The altered pruning and myeloid cell function appear to be programmed before the peripheral gustatory system is assembled and corresponds to the embryonic period when microglia progenitors derived from the yolk sac migrate to and colonize the brain.

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来源期刊
CiteScore
26.60
自引率
1.30%
发文量
189
审稿时长
3-8 weeks
期刊介绍: Since its establishment in 1896, the Journal of Experimental Medicine (JEM) has steadfastly pursued the publication of enduring and exceptional studies in medical biology. In an era where numerous publishing groups are introducing specialized journals, we recognize the importance of offering a distinguished platform for studies that seamlessly integrate various disciplines within the pathogenesis field. Our unique editorial system, driven by a commitment to exceptional author service, involves two collaborative groups of editors: professional editors with robust scientific backgrounds and full-time practicing scientists. Each paper undergoes evaluation by at least one editor from both groups before external review. Weekly editorial meetings facilitate comprehensive discussions on papers, incorporating external referee comments, and ensure swift decisions without unnecessary demands for extensive revisions. Encompassing human studies and diverse in vivo experimental models of human disease, our focus within medical biology spans genetics, inflammation, immunity, infectious disease, cancer, vascular biology, metabolic disorders, neuroscience, and stem cell biology. We eagerly welcome reports ranging from atomic-level analyses to clinical interventions that unveil new mechanistic insights.
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