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定义大鼠脑微血管中的磷酸二酯酶超家族成员。

Defining the phosphodiesterase superfamily members in rat brain microvessels.

机构信息

Division of Neurotoxicology, National Center for Toxicological Research, Food and Drug Administration, Jefferson, Arkansas 72079,United States.

出版信息

ACS Chem Neurosci. 2011 Oct 19;2(10):600-7. doi: 10.1021/cn2000487. Epub 2011 Jun 27.

Abstract

Eleven phosphodiesterase (PDE) families are known, each having several different isoforms and splice variants. Recent evidence indicates that expression of individual PDE family members is tissue-specific. Little is known concerning detailed PDE component expression in brain microvessels where the blood-brain-barrier and the local cerebral blood flow are thought to be regulated by PDEs. The present study attempted to identify PDE family members that are expressed in brain microvessels. Adult male F344 rats were sacrificed and blocks of the cerebral cortex and infratentorial areas were dissected. Microvessels were isolated using a filtration method, and total RNA was extracted. RNA quality and quantity were determined using an Agilent bioanalyzer. The isolated cortical and infratentorial microvessel total RNA amounts were 2720 ± 750 ng (n = 2) and 250 ± 40 ng (n = 2), respectively. Microarrays with 22 000 transcripts demonstrated that there were 16 PDE transcripts in the PDE superfamily, exhibiting quantifiable density in the microvessels. An additional immunofluorescent study verified that PDE4D (cAMP-specific) and PDE5A (cGMP-specific) were colocalized with RECA-1 (an endothelial marker) in the cerebral cortex using both F344 rats and Sprague-Dawley rats (n = 3-6/strain). In addition, PDE4D and PDE5A were found to be colocalized with alpha-smooth muscle actin which delineates cerebral arteries and arterioles as well as pericytes. In conclusion, a filtration method followed by microarray analyses allows PDE components to be identified in brain microvessels, and confirmed that PDE4D and PDE5A are the primary forms expressed in rat brain microvessels.

摘要

已知有 11 种磷酸二酯酶(PDE)家族,每个家族都有几个不同的同工型和剪接变体。最近的证据表明,个别 PDE 家族成员的表达具有组织特异性。关于脑微血管中 PDE 成分的详细表达情况知之甚少,而血脑屏障和局部脑血流被认为是由 PDE 调节的。本研究试图确定在脑微血管中表达的 PDE 家族成员。雄性 F344 大鼠被处死,大脑皮质和小脑下区的块被解剖。使用过滤法分离微血管,并提取总 RNA。使用 Agilent 生物分析仪测定 RNA 的质量和数量。分离的皮质和小脑下区微血管总 RNA 量分别为 2720 ± 750 ng(n = 2)和 250 ± 40 ng(n = 2)。包含 22000 个转录本的微阵列显示,PDE 超家族中有 16 个 PDE 转录本,在微血管中表现出可量化的密度。一项额外的免疫荧光研究使用 F344 大鼠和 Sprague-Dawley 大鼠(n = 3-6/品系)证实,PDE4D(cAMP 特异性)和 PDE5A(cGMP 特异性)与 RECA-1(内皮标志物)在大脑皮质中存在共定位。此外,PDE4D 和 PDE5A 被发现与 alpha-平滑肌肌动蛋白共定位,alpha-平滑肌肌动蛋白描绘了大脑动脉和小动脉以及周细胞。总之,过滤法后进行微阵列分析可在脑微血管中鉴定 PDE 成分,并证实 PDE4D 和 PDE5A 是大鼠脑微血管中主要表达的形式。

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