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血脑屏障对HIV-1反式激活因子的通透性

Permeability of the blood-brain barrier to HIV-1 Tat.

作者信息

Banks William A, Robinson Sandra M, Nath Avindra

机构信息

Division of Geriatrics, Department of Internal Medicine, GRECC, Veterans Affairs Medical Center-St. Louis and Saint Louis University School of Medicine, 915 N. Grand Boulevard, St. Louis, MO 63106, USA.

出版信息

Exp Neurol. 2005 May;193(1):218-27. doi: 10.1016/j.expneurol.2004.11.019.

Abstract

Infection with human immunodeficiency virus-1 (HIV-1) is associated with dysfunctions of the central nervous system (CNS). HIV-1 induces its effects on the CNS by a variety of mechanisms, including by shedding the neurotoxic viral proteins such as gp120 and Tat. Both HIV-1 and gp120 have been shown to cross the blood-brain barrier (BBB). It is has not been determined, however, whether blood-borne Tat can cross the BBB. Here, we found that Tat crosses the BBB by a nonsaturable mechanism with a unidirectional influx rate of about 0.490 microl/g/min. About 0.126% of an intravenous dose of Tat enters each g of brain. Radioactively labeled albumin injected simultaneously did not cross the BBB. The hypothalamus, occipital cortex, and hippocampus were the regions of the brain most permeable to Tat. Nonsaturable brain-to-blood efflux also occurred, most likely with reabsorption into the blood of the cerebrospinal fluid. In conclusion, we found that Tat crossed the BBB bidirectionally. Such permeability could provide a mechanism by which Tat produced on one side of the BBB could affect neural or immune function on the other side.

摘要

人类免疫缺陷病毒1型(HIV-1)感染与中枢神经系统(CNS)功能障碍有关。HIV-1通过多种机制对中枢神经系统产生影响,包括释放神经毒性病毒蛋白,如gp120和Tat。HIV-1和gp120均已被证明可穿过血脑屏障(BBB)。然而,血源性Tat是否能穿过血脑屏障尚未确定。在此,我们发现Tat以非饱和机制穿过血脑屏障,单向流入速率约为0.490微升/克/分钟。静脉注射剂量的Tat约有0.126%进入每克脑组织。同时注射的放射性标记白蛋白未穿过血脑屏障。下丘脑、枕叶皮质和海马体是大脑中对Tat渗透性最高的区域。也发生了非饱和的脑向血流出,很可能是脑脊液被重新吸收回血液中。总之,我们发现Tat双向穿过血脑屏障。这种通透性可能提供了一种机制,通过该机制在血脑屏障一侧产生的Tat可影响另一侧的神经或免疫功能。

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