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分子密码与食欲肽和黑色素聚集激素神经元的体外生成。

Molecular codes and in vitro generation of hypocretin and melanin concentrating hormone neurons.

机构信息

Department of Physiology, Faculty of Biology and Medicine, University of Lausanne, 1005 Lausanne, Switzerland;

Center for Integrative Genomics, Faculty of Biology and Medicine, University of Lausanne, 1015 Lausanne, Switzerland.

出版信息

Proc Natl Acad Sci U S A. 2019 Aug 20;116(34):17061-17070. doi: 10.1073/pnas.1902148116. Epub 2019 Aug 2.

Abstract

Hypocretin/orexin (HCRT) and melanin concentrating hormone (MCH) neuropeptides are exclusively produced by the lateral hypothalamus and play important roles in sleep, metabolism, reward, and motivation. Loss of HCRT (ligands or receptors) causes the sleep disorder narcolepsy with cataplexy in humans and in animal models. How these neuropeptides are produced and involved in diverse functions remain unknown. Here, we developed methods to sort and purify HCRT and MCH neurons from the mouse late embryonic hypothalamus. RNA sequencing revealed key factors of fate determination for HCRT (, , , , and ) and MCH (, , and ) neurons. Loss of in mice significantly reduces HCRT and MCH cell numbers, while knock-down of a ortholog in zebrafish completely abolishes their expression, resulting in a 2-fold increase in sleep amount. We also found that loss of HCRT neurons in mice results in a specific 50% decrease in another orexigenic neuropeptide, QRFP, that might explain the metabolic syndrome in narcolepsy. The transcriptome results were used to develop protocols for the production of HCRT and MCH neurons from induced pluripotent stem cells and ascorbic acid was found necessary for HCRT and BMP7 for MCH cell differentiation. Our results provide a platform to understand the development and expression of HCRT and MCH and their multiple functions in health and disease.

摘要

下丘脑泌素/食欲素(HCRT)和黑色素浓缩激素(MCH)神经肽仅由下丘脑外侧产生,在睡眠、代谢、奖赏和动机中发挥重要作用。HCRT(配体或受体)的缺失会导致人类和动物模型中的嗜睡症伴猝倒。这些神经肽如何产生以及如何参与多种功能仍然未知。在这里,我们开发了从小鼠晚期胚胎下丘脑分离和纯化 HCRT 和 MCH 神经元的方法。RNA 测序揭示了 HCRT(、、、和)和 MCH(、和)神经元命运决定的关键因素。在小鼠中敲除 会显著减少 HCRT 和 MCH 细胞数量,而在斑马鱼中敲低一个 同源物则完全消除了它们的表达,导致睡眠量增加 2 倍。我们还发现,在 小鼠中敲除 HCRT 神经元会导致另一种食欲肽 QRFP 特异性减少 50%,这可能解释了嗜睡症中的代谢综合征。转录组结果被用于开发诱导多能干细胞产生 HCRT 和 MCH 神经元的方案,并且发现抗坏血酸对于 HCRT 和 BMP7 对于 MCH 细胞分化是必需的。我们的研究结果为理解 HCRT 和 MCH 的发育和表达以及它们在健康和疾病中的多种功能提供了一个平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce6d/6708384/05d8c7c8e635/pnas.1902148116fig01.jpg

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