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类固醇受体辅激活因子-1:连接大脑和脊髓中多种信号与功能的核心中介物。

Steroid receptor coactivator-1: The central intermediator linking multiple signals and functions in the brain and spinal cord.

作者信息

Meng Zhaoyou, Wang Xiaoya, Zhang Dongmei, Lan Zhen, Cai Xiaoxia, Bian Chen, Zhang Jiqiang

机构信息

Department of Neurobiology, Army Medical University, Chongqing 400038, PR China.

Department of Neurosurgery, Nanchong Central Hospital, the Second Clinical Medical College, North Sichuan Medical College, Nanchong, Sichuan 637000, PR China.

出版信息

Genes Dis. 2021 Jul 13;9(5):1281-1289. doi: 10.1016/j.gendis.2021.06.009. eCollection 2022 Sep.

DOI:10.1016/j.gendis.2021.06.009
PMID:35873031
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9293692/
Abstract

The effects of steroid hormones are believed to be mediated by their nuclear receptors (NRs). The p160 coactivator family, including steroid receptor coactivator-1 (SRC-1), 2 and 3, has been shown to physically interact with NRs to enhance their transactivational activities. Among which SRC-1 has been predominantly localized in the central nervous system including brain and spinal cord. It is not only localized in neurons but also detectable in neuroglial cells (mainly localized in the nuclei but also detectable in the extra-nuclear components). Although the expression of SRC-1 is regulated by many steroids, it is also regulated by some non-steroidal factors such as injury, sound and light. Functionally, SRC-1 has been implied in normal function such as development and ageing, learning and memory, central regulation on reproductive behaviors, motor and food intake. Pathologically, SRC-1 may play a role in the regulation of neuropsychiatric disorders (including stress, depression, anxiety, and autism spectrum disorder), metabolite homeostasis and obesity as well as tumorigenesis. Under most conditions, the related mechanisms are far from elucidation; although it may regulate spatial memory through Rictor/mTORC2-actin polymerization related synaptic plasticity. Several inhibitors and stimulator of SRC-1 have shown anti-cancer potentials, but whether these small molecules could be used to modulate ageing and central disorder related neuropathology remain unclear. Therefore, to elucidate when and how SRC-1 is turned on and off under different stimuli is very interesting and great challenge for neuroscientists.

摘要

类固醇激素的作用被认为是由其核受体(NRs)介导的。p160共激活因子家族,包括类固醇受体共激活因子-1(SRC-1)、2和3,已被证明能与核受体发生物理相互作用,以增强其转录激活活性。其中,SRC-1主要定位于包括脑和脊髓在内的中枢神经系统。它不仅定位于神经元,在神经胶质细胞中也可检测到(主要定位于细胞核,但在核外成分中也可检测到)。尽管SRC-1的表达受多种类固醇调节,但也受一些非甾体因素如损伤、声音和光线的调节。在功能上,SRC-1参与了诸如发育和衰老、学习和记忆、生殖行为的中枢调节、运动和食物摄入等正常功能。在病理方面,SRC-1可能在神经精神疾病(包括应激、抑郁、焦虑和自闭症谱系障碍)、代谢物稳态和肥胖以及肿瘤发生的调节中发挥作用。在大多数情况下,相关机制远未阐明;尽管它可能通过Rictor/mTORC2-肌动蛋白聚合相关的突触可塑性来调节空间记忆。几种SRC-1的抑制剂和刺激剂已显示出抗癌潜力,但这些小分子是否可用于调节衰老和中枢性疾病相关的神经病理学仍不清楚。因此,阐明SRC-1在不同刺激下何时以及如何开启和关闭,对神经科学家来说是非常有趣且极具挑战性的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/509c/9293692/b2ddf5d9c2dc/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/509c/9293692/beb018b9305b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/509c/9293692/b2ddf5d9c2dc/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/509c/9293692/beb018b9305b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/509c/9293692/b2ddf5d9c2dc/gr2.jpg

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