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小胶质细胞对于哺乳期暴露于母体高脂饮食的后代下丘脑弓状核促食欲素神经元(AgRP)神经支配的发育特化是必需的。

Microglia are Required for Developmental Specification of AgRP Innervation in the Hypothalamus of Offspring Exposed to Maternal High-Fat Diet During Lactation.

作者信息

Mendoza-Romero Haley N, Biddinger Jessica E, Bedenbaugh Michelle N, Simerly Richard B

机构信息

Dept of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, TN, 37232, USA.

出版信息

bioRxiv. 2025 Feb 22:2024.08.12.607566. doi: 10.1101/2024.08.12.607566.

Abstract

Agouti-related peptide (AgRP) neurons in the arcuate nucleus of the hypothalamus respond to multiple metabolic signals and distribute neuroendocrine information to other brain regions such as the paraventricular hypothalamic nucleus (PVH), which plays a central role in metabolic homeostasis. Neural projections from AgRP neurons to the PVH form during the postnatal lactational period in mice and these projections are reduced in offspring of dams that consumed a high-fat diet (HFD) during lactation (MHFD-L). Here we used immunohistochemistry to visualize microglial morphology in MHFD-L offspring and identified changes that were regionally localized to the PVH and appeared temporally restricted to the period when AgRP neurons innervate this region. In addition, axon labeling experiments revealed that microglia engulf AgRP terminals in the PVH, and that the density of AgRP innervation to the PVH in MHFD-L offspring may be dependent on microglia, because microglial depletion blocked the decrease in PVH AgRP innervation observed in MHFD-L offspring, as well as prevented the increased body weight exhibited at weaning. Together, these findings suggest that microglia are activated by exposure to MHFD-L and interact directly with AgRP axons during postnatal development to permanently alter innervation of the PVH, with implications for developmental programming of metabolic phenotype.

摘要

下丘脑弓状核中的刺鼠相关肽(AgRP)神经元对多种代谢信号作出反应,并将神经内分泌信息传递到其他脑区,如下丘脑室旁核(PVH),其在代谢稳态中起核心作用。在小鼠出生后的哺乳期,AgRP神经元到PVH的神经投射形成,并且在哺乳期食用高脂饮食(HFD)的母鼠后代(MHFD-L)中,这些投射减少。在这里,我们使用免疫组织化学来观察MHFD-L后代中小胶质细胞的形态,并确定了区域定位在PVH且在时间上局限于AgRP神经元支配该区域的时期的变化。此外,轴突标记实验表明,小胶质细胞吞噬PVH中的AgRP终末,并且MHFD-L后代中PVH的AgRP神经支配密度可能依赖于小胶质细胞,因为小胶质细胞耗竭可阻止在MHFD-L后代中观察到的PVH中AgRP神经支配的减少,以及预防断奶时体重增加。总之,这些发现表明,小胶质细胞在出生后发育过程中因暴露于MHFD-L而被激活,并直接与AgRP轴突相互作用,从而永久性地改变PVH的神经支配,这对代谢表型的发育编程具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ab/11867501/5ccdd8b07b80/nihpp-2024.08.12.607566v2-f0001.jpg

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