Burchard G D, Prange G, Mirelman D
Bernhard Nocht Institute for Tropical Medicine, Clinical Department, Hamburg, Germany.
Parasitol Res. 1993;79(2):140-5. doi: 10.1007/BF00932260.
Studies on the interaction between trophozoites of Entamoeba histolytica of pathogenic or non-pathogenic origin and epithelial cells of the human intestine can contribute to the understanding of the pathogenesis of invasive amoebiasis. We have examined the interaction of virulent E. histolytica with the human colonic carcinoma cell line HT-29. Differentiated HT-29 cells are comparable to the mucosa cells to which E. histolytica attaches physiologically. Adherence between E. histolytica trophozoites and HT-29 cells was effectively inhibited by glycoconjugates containing galactose, indicating the importance of the 170-kDa lectin of E. histolytica in binding to intestinal cells. Adherence was not significantly inhibited by glycoconjugates containing N-acetyl-glucosamine, indicating that the 220-kDa lectin of E. histolytica is not involved in binding to HT-29 cells. The destruction of HT-29 cells by pathogenic E. histolytica was dependent on adherence. The destruction was enhanced when polymorphonuclear granulocytes were added to the E. histolytica trophozoites.
对致病性或非致病性溶组织内阿米巴滋养体与人肠道上皮细胞之间相互作用的研究,有助于理解侵袭性阿米巴病的发病机制。我们已经研究了毒力强的溶组织内阿米巴与人类结肠癌细胞系HT - 29之间的相互作用。分化后的HT - 29细胞与溶组织内阿米巴在生理上附着的黏膜细胞具有可比性。含有半乳糖的糖缀合物可有效抑制溶组织内阿米巴滋养体与HT - 29细胞之间的黏附,这表明溶组织内阿米巴170 kDa凝集素在与肠道细胞结合中具有重要作用。含有N - 乙酰葡糖胺的糖缀合物对黏附没有显著抑制作用,这表明溶组织内阿米巴220 kDa凝集素不参与与HT - 29细胞的结合。致病性溶组织内阿米巴对HT - 29细胞的破坏取决于黏附。当向溶组织内阿米巴滋养体中加入多形核粒细胞时,破坏作用增强。