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In vitro model of attachment of Giardia intestinalis trophozoites to IEC-6 cells an intestinal cell line.

机译:贾第鞭毛虫营养体与肠道细胞系IEC-6细胞结合的体外模型。

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摘要

Attachment of giardias to intestinal cells has been difficult to study because of a lack of a convenient in vitro model. We developed an assay for attachment of radiolabeled trophozoites to IEC-6 cells that can be done in microtiter trays. Attachment was confirmed by scanning and transmission electron microscopy. Trophozoites remained attached to the IEC-6 cells for 24 h with little evidence of damage to the IEC-6 cells. Preincubation of trophozoites with cytochalasins A, B, and D reduced attachment to approximately 20% of that of controls, whereas colchicine had no effect. Chelation of divalent cations with EDTA and EGTA [ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid] reduced attachment to 24 and 26% of control values, respectively, and incubation at 4 degrees C reduced attachment to 7% of the value for controls incubated at 37 degrees C. Glutaraldehyde fixation of trophozoites or IEC-6 cells resulted in significantly diminished attachment to the live substrate (17 and 40% of control values, respectively). Coincubation of IEC-6 cells and trophozoites on a rotary shaker resulted in detachment of 40% of trophozoites, but EDTA, EGTA, glutaraldehyde fixation of trophozoites, and low temperature diminished attachment markedly and significantly. Similar results were obtained in selected experiments with three strains of giardia.
机译:由于缺乏便利的体外模型,很难将贾第鞭毛虫附着在肠细胞上。我们开发了一种将放射性标记的滋养体附着到IEC-6细胞的测定方法,该方法可以在微量滴定盘中完成。通过扫描和透射电子显微镜确认附着。滋养体可依附在IEC-6细胞上24小时,几乎没有损坏IEC-6细胞的证据。滋养体与细胞松弛素A,B和D的预孵育将附着力降低至对照组的约20%,而秋水仙碱则没有作用。二价阳离子与EDTA和EGTA的螯合[乙二醇-双(β-氨基乙基醚)-N,N,N',N'-四乙酸]的附着力分别降低至对照值的24%和26%,并在4℃温育摄氏度降低了对37℃温育对照的附着率,至值的7%。滋养体或IEC-6细胞的戊二醛固定导致与活底物的附着力显着降低(分别为对照值的17%和40%)。在旋转摇床上对IEC-6细胞和滋养体进行共孵育会导致40%的滋养体脱离,但EDTA,EGTA,滋养体的戊二醛固定和低温显着且显着地减少了附着。在使用三种贾第虫菌株的选定实验中获得了相似的结果。

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