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本文引用的文献

1
GFAP promoter elements required for region-specific and astrocyte-specific expression.区域特异性和星形胶质细胞特异性表达所需的GFAP启动子元件。
Glia. 2008 Apr;56(5):481-93. doi: 10.1002/glia.20622.
2
Effect of penetrating brain injury on aquaporin-4 expression using a rat model.使用大鼠模型研究穿透性脑损伤对水通道蛋白4表达的影响。
J Neurotrauma. 2007 Oct;24(10):1609-17. doi: 10.1089/neu.2007.0301.
3
Human astrocytes express aquaporin-1 and aquaporin-4 in vitro and in vivo.人类星形胶质细胞在体外和体内均表达水通道蛋白-1和水通道蛋白-4。
Neuropathology. 2007 Jun;27(3):245-56. doi: 10.1111/j.1440-1789.2007.00774.x.
4
The roles of aquaporin-4 in brain edema following neonatal hypoxia ischemia and reoxygenation in a cultured rat astrocyte model.水通道蛋白4在新生大鼠缺氧缺血及复氧后培养星形胶质细胞模型脑水肿中的作用
Glia. 2007 Jul;55(9):935-41. doi: 10.1002/glia.20515.
5
Expression pattern of the water channel aquaporin-4 in human gliomas is associated with blood-brain barrier disturbance but not with patient survival.水通道蛋白4在人脑胶质瘤中的表达模式与血脑屏障紊乱有关,但与患者生存率无关。
J Neurosci Res. 2007 May 1;85(6):1336-46. doi: 10.1002/jnr.21224.
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.
7
Temporary loss of perivascular aquaporin-4 in neocortex after transient middle cerebral artery occlusion in mice.小鼠大脑中动脉短暂闭塞后新皮质血管周围水通道蛋白-4的短暂缺失
Proc Natl Acad Sci U S A. 2006 Sep 5;103(36):13532-6. doi: 10.1073/pnas.0605796103. Epub 2006 Aug 28.
8
Astrocytic expression of transgene in the rat brain mediated by baculovirus vectors containing an astrocyte-specific promoter.由含有星形胶质细胞特异性启动子的杆状病毒载体介导的转基因在大鼠脑中的星形胶质细胞表达。
Gene Ther. 2006 Oct;13(20):1447-56. doi: 10.1038/sj.gt.3302771. Epub 2006 May 25.
9
Magnesium restores altered aquaporin-4 immunoreactivity following traumatic brain injury to a pre-injury state.镁可将创伤性脑损伤后改变的水通道蛋白-4免疫反应性恢复到损伤前状态。
Acta Neurochir Suppl. 2006;96:402-6. doi: 10.1007/3-211-30714-1_83.
10
Three distinct roles of aquaporin-4 in brain function revealed by knockout mice.基因敲除小鼠揭示水通道蛋白4在脑功能中的三种不同作用。
Biochim Biophys Acta. 2006 Aug;1758(8):1085-93. doi: 10.1016/j.bbamem.2006.02.018. Epub 2006 Mar 10.

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.

DOI:10.1074/jbc.M801425200
PMID:18375385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2397463/
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。