Astrocyte Extracellular Matrix Modulates Neuronal Dendritic Development.

IF 5.4 2区 医学 Q1 NEUROSCIENCES
Glia Pub Date : 2025-04-07 DOI:10.1002/glia.70020
Joel G Hashimoto, Nicholas Margolies, Xiaolu Zhang, Joshua Karpf, Yuefan Song, Natalie Gorham, Brett A Davis, Fuming Zhang, Robert J Linhardt, Lucia Carbone, Marina Guizzetti
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Abstract

Major developmental events occurring in the hippocampus during the third trimester of human gestation and neonatally in altricial rodents include rapid and synchronized dendritic arborization and astrocyte proliferation and maturation. We tested the hypothesis that signals sent by developing astrocytes to developing neurons modulate dendritic development in vivo. First, we altered neuronal development by exposing neonatal (third trimester-equivalent) mice to ethanol, which increased dendritic arborization in hippocampal pyramidal neurons. We next assessed concurrent changes in the mouse astrocyte translatome by translating ribosomal affinity purification (TRAP)-seq. We followed up on ethanol-inhibition of astrocyte Chpf2 and Chsy1 gene translation because these genes encode biosynthetic enzymes of chondroitin sulfate glycosaminoglycan (CS-GAG) chains (extracellular matrix components that inhibit neuronal development and plasticity) and have not been explored before for their roles in dendritic arborization. We report that Chpf2 and Chsy1 are enriched in astrocytes, and their translation is inhibited by ethanol, which also reduces the levels of CS-GAGs measured by Liquid Chromatography/Mass Spectrometry. Finally, astrocyte-conditioned medium derived from Chfp2-silenced astrocytes increased neurite length and branching of hippocampal neurons in vitro, mechanistically linking changes in CS-GAG biosynthetic enzymes in astrocytes to altered neuronal development. These results demonstrate that CS-GAG biosynthetic enzymes in astrocytes regulate dendritic arborization in developing neurons and are involved in ethanol-induced altered neuronal development.

星形胶质细胞外基质调节神经元树突发育。
在人类妊娠晚期和晚熟啮齿类动物的新生儿中,海马发生的主要发育事件包括快速和同步的树突树突形成和星形胶质细胞的增殖和成熟。我们在体内测试了星形胶质细胞向神经元发送信号调节树突发育的假设。首先,我们通过将新生小鼠(相当于妊娠晚期)暴露于乙醇中来改变神经元的发育,乙醇增加了海马锥体神经元的树突树突。接下来,我们通过翻译核糖体亲和纯化(TRAP)-seq来评估小鼠星形胶质细胞翻译组的并发变化。我们后续研究了乙醇对星形胶质细胞Chpf2和Chsy1基因翻译的抑制作用,因为这些基因编码硫酸软骨素糖胺聚糖(CS-GAG)链(抑制神经元发育和可塑性的细胞外基质成分)的生物合成酶,之前还没有研究过它们在树突状乔木化中的作用。我们报道了Chpf2和Chsy1在星形胶质细胞中富集,并且它们的翻译被乙醇抑制,这也降低了液相色谱/质谱测定的CS-GAGs水平。最后,由chfp2沉默的星形胶质细胞衍生的星形胶质细胞条件培养基在体外增加了海马神经元的神经突长度和分支,将星形胶质细胞中CS-GAG生物合成酶的变化与神经元发育的改变机械地联系起来。这些结果表明星形胶质细胞中的CS-GAG生物合成酶调节发育中的神经元的树突树突形成,并参与了乙醇诱导的神经元发育改变。
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
Glia
Glia 医学-神经科学
CiteScore
13.10
自引率
4.80%
发文量
162
审稿时长
3-8 weeks
期刊介绍: GLIA is a peer-reviewed journal, which publishes articles dealing with all aspects of glial structure and function. This includes all aspects of glial cell biology in health and disease.
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