凝集素在牛眼前段的结合。

The Histochemical Journal Pub Date : 1994-10-01
A Tuori, I Virtanen, H Uusitalo
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引用次数: 0

摘要

使用11种不同的荧光凝集素偶联物来揭示牛眼睛前段冷冻切片中碳水化合物残基的位置。凝集素对以下5个主要碳水化合物组具有特异性:(1)葡萄糖/甘露糖组(cona);(2) n -乙酰氨基葡萄糖(小麦胚芽凝集素);(3)半乳糖/ n-乙酰半乳糖胺组(Dolichos biflorus凝集素(DBA)、Helix pomatia凝集素(HPA)、Helix aspersa凝集素(HAA)、phocarpus tetragonolobus凝集素(PTA)、Griffonia simplicifolia凝集素- i - b4 (GSA-I-B4)、Artocarpus integrifolia凝集素(JAC)、peanut凝集素(PNA)和Ricinus communis凝集素(RCA-I));(4) L-焦点组(UEA-I);(5)唾液酸基团(小麦胚芽凝集素(WGA))。除uea - 1外,所有凝集素均与不同结构广泛反应,结果表明,牛眼前段碳水化合物残基的表达模式不同。uea - 1仅与上皮结构结合。一些凝集素与结膜上皮和角膜上皮的顶端细胞表面反应非常强烈,表明上皮的糖萼有不同的糖基化。此外,结膜上皮和角膜上皮的结合模式与某些凝集素不同:PNA和RCA-I完全不结合,GSA-I-B4仅与角膜上皮结合非常弱,而它们与结膜上皮结合。此外,HPA、HAA、PNA和WGA不与角膜基底膜结合,而与结膜和血管基底膜结合。这表明角膜基底膜与其他基底膜有某种不同。具有相同碳水化合物特异性的凝集素(DBA、HPA、HAA和PTA)与切片的反应几乎相同,但存在一些差异:DBA不与结膜和巩膜的基底膜结合,但与角膜的基底膜结合,而具有相同碳水化合物特异性的其他凝集素则相反。此外,PTA与小梁网的结合可以忽略不计,而具有相同碳水化合物特异性的其他凝集素与小梁网反应。GSA-I-B4与血管内皮反应强烈,不与基质结合,使血管非常突出,可作为内皮标记物。这种凝集素也与角膜内皮发生强烈反应。因此,GSA-I-B4似乎是牛组织中血管和角膜内皮细胞的特异性标记物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lectin binding in the anterior segment of the bovine eye.

Eleven different fluorescent lectin-conjugates were used to reveal the location of carbohydrate residues in frozen sections of the anterior segment of bovine eyes. The lectins were specific for the following five major carbohydrate groups: (1) glucose/mannose group (Concanavalin A (Con A)); (2) N-acetylglucosamine group (wheat germ agglutinin (WGA)); (3) galactose/N-acetylgalactosamine group (Dolichos biflorus agglutinin (DBA), Helix pomatia agglutinin (HPA), Helix aspersa agglutinin (HAA), Psophocarpus tetragonolobus agglutinin (PTA), Griffonia simplicifolia agglutinin-I-B4 (GSA-I-B4), Artocarpus integrifolia agglutinin (JAC), peanut agglutinin (PNA) and Ricinus communis agglutinin (RCA-I)); (4) L-fucose group (Ulex europaeus agglutinin (UEA-I)); (5) sialic acid group (wheat germ agglutinin (WGA)). All the studied lectins except UEA-I reacted widely with different structures and the results suggest that there are distinct patterns of expression of carbohydrate residues in the anterior segment of the bovine eye. UEA-I bound only to epithelial structures. Some of the lectins reacted very intensely with apical cell surfaces of conjunctival and corneal epithelia suggesting a different glycosylation at the glycocalyx of the epithelia. Also, the binding patterns of conjunctival and corneal epithelia differed with some of the lectins: PNA and RCA-I did not bind at all, and GSA-I-B4 bound only very weakly to the epithelium of the cornea, whereas they bound to the epithelium of the conjunctiva. In addition, HPA, HAA, PNA and WGA did not bind to the corneal basement membrane, but bound to the conjunctiva and vascular basement membranes. This suggests that corneal basement membrane is somehow different from other basement membranes. Lectins with the same carbohydrate specificity (DBA, HPA, HAA and PTA) reacted with the sections almost identically, but some differences were noticed: DBA did not bind to the basement membrane of the conjunctiva and the sclera and did bind to the basement membrane of the cornea, whereas other lectins with same carbohydrate specificities reacted vice versa. Also, the binding of PTA to the trabecular meshwork was negligible, whereas other lectins with the same carbohydrate specificities reacted with the trabecular meshwork. GSA-I-B4 reacted avidly with the endothelium of blood vessels and did not bind to the stroma, so that it made blood vessels very prominent and it might be used as an endothelial marker. This lectin also reacted avidly with the corneal endothelium. Therefore, GSA-I-B4 appears to be a specific marker in bovine tissues for both blood vessel and corneal endothelium cells.

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