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使用平滑肌分化标志物对小动脉发育进行免疫组织化学鉴定。毛细血管动脉化从终末小动脉开始的证据。

Immunohistochemical identification of arteriolar development using markers of smooth muscle differentiation. Evidence that capillary arterialization proceeds from terminal arterioles.

作者信息

Price R J, Owens G K, Skalak T C

机构信息

Department of Biomedical Engineering, University of Virginia, Charlottesville 22908.

出版信息

Circ Res. 1994 Sep;75(3):520-7. doi: 10.1161/01.res.75.3.520.

DOI:10.1161/01.res.75.3.520
PMID:8062425
Abstract

Arteriolar growth is an important event in the adaptation of normal tissues as well as in important pathologies, but the site of origin of new arterioles remains unknown. The network pattern of arteriolar development in skeletal muscle was detected by use of a new immunohistochemical technique that is based on the observation that fully differentiated (mature) vascular smooth muscle (SM) cells express both SM alpha-actin and the two myosin heavy chains (MHCs) SM-1 and SM-2, whereas less differentiated (immature) vascular SM cells do not express MHC. The anterior gracilis muscle microvasculatures of 4- and 9-week-old Sprague-Dawley rats were labeled with monoclonal antibodies to SM alpha-actin and to SM MHC. Whole transverse arteriole networks were observed, and terminal arterioles, defined as terminal segments labeled with SM alpha-actin, were classified on the basis of the presence or absence of SM MHC. A significantly different percentage of terminal arteriolar endings per network without SM MHC was observed in the two groups (66.1 +/- 17.3% for 4 weeks and 27.1 +/- 18.5% for 9 weeks), suggesting that arteriolar development is more nearly complete in the older animals. Sparsely distributed capillaries exhibited thin extensions of SM alpha-actin that crossed collecting venules and joined similar extensions from an adjacent transverse arteriole, effectively forming the basis for new arcade arterioles. SM alpha-actin and SM MHC labeling in terminal arterioles was always continuous with upstream arterioles.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

小动脉生长是正常组织适应以及重要病理过程中的一个重要事件,但新小动脉的起源部位仍然未知。利用一种新的免疫组织化学技术检测骨骼肌中小动脉发育的网络模式,该技术基于这样的观察:完全分化(成熟)的血管平滑肌(SM)细胞同时表达SMα-肌动蛋白和两种肌球蛋白重链(MHCs)SM-1和SM-2,而分化程度较低(不成熟)的血管SM细胞不表达MHC。用抗SMα-肌动蛋白和抗SM MHC的单克隆抗体标记4周龄和9周龄Sprague-Dawley大鼠的股薄肌前部微血管。观察整个横向小动脉网络,并将定义为用SMα-肌动蛋白标记的终末段的终末小动脉根据SM MHC的有无进行分类。在两组中观察到每个网络中无SM MHC的终末小动脉末梢百分比有显著差异(4周龄为66.1±17.3%,9周龄为27.1±18.5%),这表明老年动物的小动脉发育更接近完成。稀疏分布的毛细血管呈现出SMα-肌动蛋白的细延伸,其穿过集合小静脉并与相邻横向小动脉的类似延伸相连,有效地形成了新的弓状小动脉的基础。终末小动脉中的SMα-肌动蛋白和SM MHC标记总是与上游小动脉连续。(摘要截短于250字)

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