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肠道氮能神经元密度的个体间差异受 GDNF 水平和 ETV1 的调节。

Interindividual Variation in Gut Nitrergic Neuron Density Is Regulated By GDNF Levels and ETV1.

机构信息

Translational Neuroscience, Department of Pharmacology, Faculty of Medicine and Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland; Department of Pharmacology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.

Department of Pharmacology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.

出版信息

Cell Mol Gastroenterol Hepatol. 2024;18(6):101405. doi: 10.1016/j.jcmgh.2024.101405. Epub 2024 Sep 17.

Abstract

BACKGROUND & AIMS: The size and function of the enteric nervous system (ENS) can vary substantially between individuals. Because ENS function is involved in the etiology of a growing number of common human diseases, understanding mechanisms that regulate ENS variation is important.

METHODS

We analyzed RNAseq data from 41 normal adult human colon biopsies and single-cell RNA-seq data from human and mouse developing gut. To establish cause-consequence relationship we used alleles in mice that allow levels change of the candidate effector molecule in the comparable range to human samples. We used siRNA and primary neuronal cultures to define downstream molecular events and characterized gut functional changes in mice where molecular phenotypes paralleled findings in humans.

RESULTS

We found that glial cell line-derived neurotrophic factor (GDNF) levels in the human colon vary about 5-fold and correlate strongly with nitrergic marker expression. In mice, we defined that GDNF levels are regulated via its 3' untranslated region (3' UTR) in the gastrointestinal tract and observed similar correlation between GDNF levels and nitrergic lineage development. We identified miR-9 and miR-133 as evolutionarily conserved candidates for negative regulation of GDNF expression in the gastrointestinal tract. Functionally, an increase in inhibitory nitrergic innervation results in an increase in gastrointestinal tract transit time, stool size, and water content accompanied with modestly reduced epithelial barrier function. Mechanistically, we found that GDNF levels regulate nitrergic lineage development via induction of transcription factor ETV1, corroborated by single-cell gene expression data in human and mouse developing enteric neurons.

CONCLUSIONS

Our results reveal how normal variation in GDNF levels influence ENS size, composition, and gut function, suggesting a mechanism for well-known interindividual variation among those parameters.

摘要

背景与目的

肠神经系统(ENS)的大小和功能在个体之间可能有很大差异。由于 ENS 功能与越来越多常见人类疾病的病因有关,因此了解调节 ENS 变异的机制非常重要。

方法

我们分析了 41 例正常成人结肠活检的 RNAseq 数据和人类和小鼠发育肠道的单细胞 RNA-seq 数据。为了建立因果关系,我们使用了能够使候选效应分子的水平在与人类样本可比范围内发生变化的小鼠等位基因。我们使用 siRNA 和原代神经元培养物来定义下游分子事件,并在分子表型与人类相似的小鼠中描述了肠道功能变化。

结果

我们发现人类结肠中的胶质细胞源性神经营养因子(GDNF)水平变化约 5 倍,与氮能标记物表达强烈相关。在小鼠中,我们定义了 GDNF 水平通过其胃肠道的 3'非翻译区(3'UTR)进行调节,并且在 GDNF 水平和氮能谱系发育之间观察到类似的相关性。我们鉴定出 miR-9 和 miR-133 作为胃肠道中 GDNF 表达负调控的进化保守候选物。在功能上,抑制性氮能传入神经的增加导致胃肠道转运时间、粪便大小和含水量增加,同时伴有轻微的上皮屏障功能降低。在机制上,我们发现 GDNF 水平通过诱导转录因子 ETV1 来调节氮能谱系的发育,这与人类和小鼠发育肠神经元的单细胞基因表达数据相吻合。

结论

我们的结果揭示了 GDNF 水平的正常变化如何影响 ENS 的大小、组成和肠道功能,为这些参数之间众所周知的个体间差异提供了一种机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4be5/11547909/d9cba744def9/gr1.jpg

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