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不同物种晶状体中的黏着连接:采用改良固定方法的超微结构分析

Adherens junctions in the ocular lens of various species: ultrastructural analysis with an improved fixation.

作者信息

Lo W K

机构信息

Department of Anatomy, Morehouse School of Medicine, Atlanta, Georgia 30310.

出版信息

Cell Tissue Res. 1988 Oct;254(1):31-40. doi: 10.1007/BF00220014.

Abstract

The ultrastructure and distribution of adherens junctions in the intact adult lens of human, chicken, dove, rat, and rainbow trout were studied with thin-section electron microscopy, using an improved fixation containing a mixture of glutaraldehyde, lysine, and tannic acid. The nature of adherens junctions in the fiber-cells of the lens was also verified by immunofluorescence and rhodamine-phalloidin labelings for vinculin and actin. Electron microscopy revealed that adherens junctions of the lens were different ultrastructurally from the desmosomes found only between the lateral epithelial cells of the lens. The adherens junctions had the same structural characteristics as the zonulae adherentes, except that they were macular contacts, not belts. However, cross bridges were evident within the interspace of the junctions. Adherens junctions were located between the fiber-cells, between the epithelial cells and fiber-cells, and between the epithelial cells. They had a characteristic distribution in the "intersections" where three hexagonal fiber-cells met, as seen in cross-sections in all species studied. In addition, adherens junctions and associated actin were found distributed randomly along the entire cell membranes of both wide and narrow sides of cortical fiber-cells in the human, chicken, and dove lenses which have good accomodating capability. However, in the poorly-accomodating lenses of rat and fish, these junctions were seen predominantly on the narrow sides and at the regions of the wide sides that were very close to the "intersections". It is suggested that adherens junctions and associated actin microfilaments are involved in stabilizing the structural integrity of lens cells during accomodation and in preserving a specific lens shape.

摘要

利用含有戊二醛、赖氨酸和鞣酸混合物的改良固定剂,通过超薄切片电子显微镜研究了人、鸡、鸽、大鼠和虹鳟鱼完整成年晶状体中黏着连接的超微结构和分布。还通过免疫荧光以及针对纽蛋白和肌动蛋白的罗丹明 - 鬼笔环肽标记,验证了晶状体纤维细胞中黏着连接的性质。电子显微镜显示,晶状体的黏着连接在超微结构上与仅在晶状体外侧上皮细胞之间发现的桥粒不同。黏着连接具有与黏着小带相同的结构特征,只是它们是斑状连接,而非带状连接。然而,在连接的间隙内可见交叉桥。黏着连接位于纤维细胞之间、上皮细胞与纤维细胞之间以及上皮细胞之间。在所有研究物种的横截面中,它们在三个六边形纤维细胞相交的“交叉点”处具有特征性分布。此外,在具有良好调节能力的人、鸡和鸽晶状体中,黏着连接和相关的肌动蛋白沿着皮质纤维细胞宽边和窄边的整个细胞膜随机分布。然而,在调节能力较差的大鼠和鱼类晶状体中,这些连接主要见于窄边以及宽边非常靠近“交叉点”的区域。有人提出,黏着连接和相关的肌动蛋白微丝在调节过程中参与稳定晶状体细胞的结构完整性,并维持特定的晶状体形状。

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