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可扩展的从人类多能干细胞分化下丘脑弓状核神经元,适用于代谢和生殖障碍建模

Scalable Hypothalamic Arcuate Neuron Differentiation from Human Pluripotent Stem Cells Suitable for Modeling Metabolic and Reproductive Disorders.

作者信息

Jovanovic Vukasin M, Narisu Narisu, Bonnycastle Lori L, Tharakan Ravi, Mesch Kendall T, Glover Hannah J, Yan Tingfen, Sinha Neelam, Sen Chaitali, Castellano David, Yang Shu, Blivis Dvir, Ryu Seungmi, Bennett Daniel F, Rosales-Soto Giovanni, Inman Jason, Ormanoglu Pinar, LeClair Christopher A, Xia Menghang, Schneider Martin, Hernandez-Ochoa Erick O, Erdos Michael R, Simeonov Anton, Chen Shuibing, Collins Francis S, Doege Claudia A, Tristan Carlos A

机构信息

National Center for Advancing Translational Sciences (NCATS), Division of Preclinical Innovation Rockville, MD 20850, USA.

Hypothalamus Consortium.

出版信息

bioRxiv. 2024 Sep 20:2024.06.27.601062. doi: 10.1101/2024.06.27.601062.

Abstract

The hypothalamus, composed of several nuclei, is essential for maintaining our body's homeostasis. The arcuate nucleus (ARC), located in the mediobasal hypothalamus, contains neuronal populations with eminent roles in energy and glucose homeostasis as well as reproduction. These neuronal populations are of great interest for translational research. To fulfill this promise, we used a robotic cell culture platform to provide a scalable and chemically defined approach for differentiating human pluripotent stem cells (hPSCs) into pro-opiomelanocortin (POMC), somatostatin (SST), tyrosine hydroxylase (TH) and gonadotropin-releasing hormone (GnRH) neuronal subpopulations with an ARC-like signature. This robust approach is reproducible across several distinct hPSC lines and exhibits a stepwise induction of key ventral diencephalon and ARC markers in transcriptomic profiling experiments. This is further corroborated by direct comparison to human fetal hypothalamus, and the enriched expression of genes implicated in obesity and type 2 diabetes (T2D). Genome-wide chromatin accessibility profiling by ATAC-seq identified accessible regulatory regions that can be utilized to predict candidate enhancers related to metabolic disorders and hypothalamic development. In depth molecular, cellular, and functional experiments unveiled the responsiveness of the hPSC-derived hypothalamic neurons to hormonal stimuli, such as insulin, neuropeptides including kisspeptin, and incretin mimetic drugs such as Exendin-4, highlighting their potential utility as physiologically relevant cellular models for disease studies. In addition, differential glucose and insulin treatments uncovered adaptability within the generated ARC neurons in the dynamic regulation of POMC and insulin receptors. In summary, the establishment of this model represents a novel, chemically defined, and scalable platform for manufacturing large numbers of hypothalamic arcuate neurons and serves as a valuable resource for modeling metabolic and reproductive disorders.

摘要

下丘脑由多个核团组成,对维持人体的内环境稳定至关重要。位于下丘脑内侧基底部的弓状核(ARC)含有在能量和葡萄糖稳态以及生殖过程中发挥重要作用的神经元群体。这些神经元群体对于转化研究具有重要意义。为了实现这一目标,我们使用了一个机器人细胞培养平台,提供一种可扩展且化学成分明确的方法,将人类多能干细胞(hPSC)分化为具有ARC样特征的促肾上腺皮质激素原(POMC)、生长抑素(SST)、酪氨酸羟化酶(TH)和促性腺激素释放激素(GnRH)神经元亚群。这种强大的方法在多个不同的hPSC系中均可重复,并在转录组分析实验中显示出关键腹侧间脑和ARC标记物的逐步诱导。与人类胎儿下丘脑的直接比较以及肥胖和2型糖尿病(T2D)相关基因的富集表达进一步证实了这一点。通过ATAC-seq进行的全基因组染色质可及性分析确定了可用于预测与代谢紊乱和下丘脑发育相关的候选增强子的可及调控区域。深入的分子、细胞和功能实验揭示了hPSC衍生的下丘脑神经元对激素刺激(如胰岛素)、包括亲吻素在内的神经肽以及艾塞那肽-4等肠促胰岛素模拟药物的反应性,突出了它们作为疾病研究中生理相关细胞模型的潜在用途。此外,不同的葡萄糖和胰岛素处理揭示了所生成的ARC神经元在POMC和胰岛素受体动态调节中的适应性。总之,该模型的建立代表了一个新颖、化学成分明确且可扩展的平台,用于大量制造下丘脑弓状神经元,并为代谢和生殖紊乱建模提供了宝贵资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c30/11455507/30d1c3abe275/nihpp-2024.06.27.601062v2-f0001.jpg

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