Johnson B W, Whiteley H E, McLaughlin S A
Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois, Urbana 61804.
Am J Vet Res. 1990 May;51(5):820-4.
An experimental model of keratoconjunctivitis sicca (KCS) was produced by removing the lacrimal gland and the gland of the third eyelid from the left eye of 6 cats. The right eye of each cat was left intact and used as a control. After 2 weeks, cats were euthanatized and the central portion of the upper eyelid from both eyes of each cat was excised. Histologic sections were stained with either hematoxylin and eosin or with a battery of biotinylated lectins including concanavalin A (conA), soybean agglutinin (SBA), wheat germ agglutinin (WGA), succinylated wheat germ agglutinin (S-WGA), Ulex europaeus agglutinin I (UEA), Dolichos biflorus agglutinin (DBA), Ricinus communis agglutinin (RCA), peanut agglutinin (PNA), and PNA pretreated with neuraminidase. Consistent differences in histologic features were not observed between conjunctivas with KCS and control conjunctivas. A variable degree of mononuclear cell infiltration of the substantia propria was observed in control conjunctivas and those with KCS. In both groups, conjunctival goblet cell density decreased and epithelial stratification increased as the degree of submucosal inflammatory cell infiltration increased. Lectin binding sites for DBA, WGA, S-WGA, UEA, PNA, and PNA pretreated with neuraminidase were detected on conjunctival goblet cells of conjunctivas with KCS and control conjunctivas. The mucus/glycocalyx layer of conjunctival epithelial cells in both groups of conjunctivas bound lectins RCA, WGA, UEA, and conA, but inconsistently bound S-WGA. In both groups, DBA principally bound to the mucus layer overlying normal epithelium, whereas PNA pretreated with neuraminidase consistently bound to the mucus layer of stratified epithelial surfaces free of goblet cells. Binding of SBA to goblet cells and the mucus/glycocalyx layer was variable.
通过切除6只猫左眼的泪腺和第三眼睑腺体,建立了干燥性角结膜炎(KCS)的实验模型。每只猫的右眼保持完整,用作对照。2周后,对猫实施安乐死,并切除每只猫双眼上眼睑的中央部分。组织学切片用苏木精和伊红染色,或用一系列生物素化凝集素染色,包括刀豆球蛋白A(ConA)、大豆凝集素(SBA)、麦胚凝集素(WGA)、琥珀酰化麦胚凝集素(S-WGA)、欧洲荆豆凝集素I(UEA)、双花扁豆凝集素(DBA)、蓖麻凝集素(RCA)、花生凝集素(PNA)以及经神经氨酸酶预处理的PNA。KCS结膜与对照结膜之间未观察到组织学特征的一致差异。在对照结膜和KCS结膜中均观察到固有层有不同程度的单核细胞浸润。在两组中,随着黏膜下炎性细胞浸润程度的增加,结膜杯状细胞密度降低,上皮分层增加。在KCS结膜和对照结膜的结膜杯状细胞上检测到DBA、WGA、S-WGA、UEA、PNA以及经神经氨酸酶预处理的PNA的凝集素结合位点。两组结膜上皮细胞的黏液/糖萼层均与凝集素RCA、WGA、UEA和ConA结合,但与S-WGA的结合不一致。在两组中,DBA主要结合于正常上皮表面的黏液层,而经神经氨酸酶预处理的PNA始终结合于无杯状细胞的复层上皮表面的黏液层。SBA与杯状细胞及黏液/糖萼层的结合情况不一。