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SUBFORNICAL ORGAN 胰岛素受体在小鼠中的细胞特征。

Cellular Profile of Subfornical Organ Insulin Receptors in Mice.

机构信息

Department of Pharmacology and Physiology, George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA.

出版信息

Biomolecules. 2024 Oct 4;14(10):1256. doi: 10.3390/biom14101256.

DOI:10.3390/biom14101256
PMID:39456189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11506324/
Abstract

Brain insulin receptor signaling is strongly implicated in cardiovascular and metabolic physiological regulation. In particular, we recently demonstrated that insulin receptors within the subfornical organ (SFO) play a tonic role in cardiovascular and metabolic regulation in mice. The SFO is a forebrain sensory circumventricular organ that regulates cardiometabolic homeostasis due to its direct exposure to the circulation and thus its ability to sense circulating factors, such as insulin. Previous work has demonstrated broad distribution of insulin receptor-expressing cells throughout the entire SFO, indirectly indicating insulin receptor expression in multiple cell types. Based on this, we sought to determine the cellular phenotypes that express insulin receptors within the SFO by combining immunohistochemistry with genetically modified reporter mouse models. Interestingly, SFO neurons, including both excitatory and inhibitory types, were the dominant cell site for insulin receptor expression, although a weak degree of insulin receptor expression was also detected in astrocytes. Moreover, SFO angiotensin type 1a receptor neurons also expressed insulin receptors. Collectively, these anatomical findings indicate the existence of potentially complex cellular networks within the SFO through which insulin signaling can influence physiology and further point to the SFO as a possible brain site for crosstalk between angiotensin-II and insulin.

摘要

脑胰岛素受体信号在心血管和代谢生理调节中起着重要作用。特别是,我们最近证明,穹窿下器官(SFO)中的胰岛素受体在小鼠的心血管和代谢调节中起着紧张作用。SFO 是大脑前部的感觉室周器官,由于其直接暴露于循环中,因此能够感知循环因子,如胰岛素,从而调节心脏代谢稳态。先前的工作表明,胰岛素受体表达细胞广泛分布于整个 SFO 中,间接表明胰岛素受体在多种细胞类型中表达。基于此,我们通过将免疫组织化学与基因修饰报告小鼠模型相结合,试图确定 SFO 中表达胰岛素受体的细胞表型。有趣的是,SFO 神经元,包括兴奋性和抑制性神经元,是胰岛素受体表达的主要细胞部位,尽管星形胶质细胞中也检测到弱程度的胰岛素受体表达。此外,SFO 血管紧张素 1a 受体神经元也表达胰岛素受体。总之,这些解剖学发现表明 SFO 中存在潜在的复杂细胞网络,胰岛素信号可以通过这些网络影响生理学,并进一步表明 SFO 可能是血管紧张素-II 和胰岛素之间相互作用的脑区。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/1d6a5ca5a671/biomolecules-14-01256-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/f8a6c8c4a65d/biomolecules-14-01256-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/a3fbd8a357cf/biomolecules-14-01256-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/3874fc82c740/biomolecules-14-01256-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/3de1425c07c6/biomolecules-14-01256-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/727cd056b863/biomolecules-14-01256-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/1d6a5ca5a671/biomolecules-14-01256-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/f8a6c8c4a65d/biomolecules-14-01256-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/a3fbd8a357cf/biomolecules-14-01256-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/3874fc82c740/biomolecules-14-01256-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/3de1425c07c6/biomolecules-14-01256-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/727cd056b863/biomolecules-14-01256-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fb1/11506324/1d6a5ca5a671/biomolecules-14-01256-g006.jpg

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Neuropharmacology. 2023 May 15;229:109460. doi: 10.1016/j.neuropharm.2023.109460. Epub 2023 Feb 17.
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Insulin regulates neurovascular coupling through astrocytes.胰岛素通过星形胶质细胞调节神经血管耦联。
Proc Natl Acad Sci U S A. 2022 Jul 19;119(29):e2204527119. doi: 10.1073/pnas.2204527119. Epub 2022 Jul 14.
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Anatomical Organization of the Rat Subfornical Organ.
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Brain Angiotensin Type-1 and Type-2 Receptors in Physiological and Hypertensive Conditions: Focus on Neuroinflammation.脑内血管紧张素 1 型和 2 型受体在生理和高血压条件下的作用:聚焦神经炎症。
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