新生大鼠晶状体上皮通透性研究。

Lens and eye toxicity research Pub Date : 1991-01-01
N J Unakar, M J Johnson, K Hynes
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引用次数: 0

摘要

采用硝酸镧(LN)和辣根过氧化物酶(HRP)作为示踪剂,研究大鼠晶状体上皮细胞间通透性、紧密连接的存在和位置及其变化。在电子显微镜水平上研究了出生时和每隔三天从动物身上取下的透镜薄片,直到新生儿在大约22天断奶。在每个年龄段,这两种示踪剂都渗透到前区上皮的细胞间隙和赤道区纤维细胞之间。LN沉淀终止于前极区上皮的顶端附近,在该区域上皮-纤维界面或纤维之间未见。在示踪剂终止的位置,发现细胞间隙相当狭窄或完全封闭。然而,HRP沉淀物存在于这些细胞间隙中,如果存在紧密连接,通过HRP“冲洗”程序可以从上皮细胞间隙的基底外侧部位冲洗出来,直至收缩点。在小于24小时出生的动物晶状体中,紧密连接的上皮占据的晶状体面积非常小,随着新生儿年龄的增长,晶状体面积越来越大。这些发现进一步证实了成熟大鼠晶状体中央前区上皮细胞之间紧密连接形式的屏障的存在。此外,我们的观察还提供了关于晶状体成熟过程中紧密结发育和分布模式的信息。
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Permeability studies in neonatal rat lens epithelium.

Lanthanum nitrate (LN) and horseradish peroxidase (HRP) were used as tracers to study intercellular permeability as well as the existence and location of tight junctions and changes in them, if any, in the lens epithelium of Sprague Dawley rats. Thin sections of lenses taken from animals at birth and at three day intervals until the neonates were weaned at approximately 22 days were studied at the electron microscope level. At every age both tracers permeated the intercellular spaces of the anterior region epithelium and between the fiber cells of the equatorial region. The LN precipitates terminated near the apical part of the epithelium in the anterior polar region and were not seen at the epithelial-fiber interface or between fibers in this region. At the site of the tracer termination the intercellular space was found to be considerably constricted or completely sealed. The HRP precipitates, however, were present in these intercellular spaces and by using the HRP "washout" procedure could be washed out of the basolateral site of the intercellular spaces of the epithelium up to the point of constriction if a tight junction were present. The lens area occupied by epithelium with tight junctions was age related being very small in lenses from animals less than 24 hours old and becoming increasingly enlarged as the newborn aged. These findings further confirm the existence of a barrier in the form of tight junctions between epithelial cells in the central anterior region of the maturing rat lens. Moreover, our observations also provide information regarding the pattern of tight junction development and distribution during lens maturation.

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