Suppr超能文献

转基因小鼠中胶质细胞水通道蛋白4的过表达会加速细胞毒性脑肿胀。

Glial cell aquaporin-4 overexpression in transgenic mice accelerates cytotoxic brain swelling.

作者信息

Yang Baoxue, Zador Zsolt, Verkman A S

机构信息

Departments of Medicine and Physiology, University of California-San Francisco, 1246 Health Sciences East Tower, San Francisco, CA 94143-0521, USA.

出版信息

J Biol Chem. 2008 May 30;283(22):15280-6. doi: 10.1074/jbc.M801425200. Epub 2008 Mar 28.

Abstract

Aquaporin-4 (AQP4) is a water transport protein expressed in glial cell plasma membranes, including glial cell foot processes lining the blood-brain barrier. AQP4 deletion in mice reduces cytotoxic brain edema produced by different pathologies. To determine whether AQP4 is rate-limiting for brain water accumulation and whether altered AQP4 expression, as occurs in various pathologies, could have functional importance, we generated mice that overexpressed AQP4 in brain glial cells by a transgenic approach using the glial fibrillary acid protein promoter. Overexpression of AQP4 protein in brain by approximately 2.3-fold did not affect mouse survival, appearance, or behavior, nor did it affect brain anatomy or intracranial pressure (ICP). However, following acute water intoxication produced by intraperitoneal water injection, AQP4-overexpressing mice had an accelerated progression of cytotoxic brain swelling, with ICP elevation of 20 +/- 2 mmHg at 10 min, often producing brain herniation and death. In contrast, ICP elevation was 14 +/- 2 mmHg at 10 min in control mice and 9.8 +/- 2 mmHg in AQP4 knock-out mice. The deduced increase in brain water content correlated linearly with brain AQP4 protein expression. We conclude that AQP4 expression is rate-limiting for brain water accumulation, and thus, that altered AQP4 expression can be functionally significant.

摘要

水通道蛋白4(AQP4)是一种在胶质细胞质膜中表达的水转运蛋白,包括位于血脑屏障的胶质细胞足突。小鼠体内AQP4的缺失可减轻由不同病理状态产生的细胞毒性脑水肿。为了确定AQP4是否是脑水蓄积的限速因素,以及在各种病理状态下发生的AQP4表达改变是否具有功能重要性,我们通过使用胶质纤维酸性蛋白启动子的转基因方法,培育出在脑胶质细胞中过表达AQP4的小鼠。脑内AQP4蛋白过表达约2.3倍并不影响小鼠的存活、外观或行为,也不影响脑解剖结构或颅内压(ICP)。然而,在腹腔注射水导致急性水中毒后,过表达AQP4的小鼠细胞毒性脑肿胀进展加速,10分钟时颅内压升高20±2 mmHg,常导致脑疝形成和死亡。相比之下,对照小鼠在10分钟时颅内压升高14±2 mmHg,AQP4基因敲除小鼠为9.8±2 mmHg。推断的脑含水量增加与脑AQP4蛋白表达呈线性相关。我们得出结论,AQP4表达是脑水蓄积的限速因素,因此,AQP4表达改变可能具有功能重要性。

相似文献

3
Aquaporin-4 and brain edema.水通道蛋白-4与脑水肿
Pediatr Nephrol. 2007 Jun;22(6):778-84. doi: 10.1007/s00467-006-0411-0. Epub 2007 Mar 9.
9
Studies of mdx mice.杜兴氏肌营养不良症小鼠的研究。
Neuroscience. 2004;129(4):993-8. doi: 10.1016/j.neuroscience.2004.08.055.

引用本文的文献

3
Role of aquaporins in brain water transport and edema.水通道蛋白在脑水转运和水肿中的作用。
Front Neurosci. 2025 Jan 29;19:1518967. doi: 10.3389/fnins.2025.1518967. eCollection 2025.
5
Unveiling Interactions between Self-Assembling Peptides and Neuronal Membranes.揭示自组装肽与神经元膜之间的相互作用。
Langmuir. 2024 Dec 24;40(51):26811-26823. doi: 10.1021/acs.langmuir.4c02050. Epub 2024 Dec 9.

本文引用的文献

6
Abnormalities in the pattern of AQP4 immunoreactivity.
FASEB J. 2006 Nov;20(13):2423-4; author reply 2425. doi: 10.1096/fj.06-1104ufm.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验