Erlandsen Stanley L, Russo A Peter, Turner James N
Department of Genetics, Cell and Developmental Biology, 6-160 Jackson Hall, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
J Eukaryot Microbiol. 2004 Jan-Feb;51(1):73-80. doi: 10.1111/j.1550-7408.2004.tb00165.x.
Giardia lamblia is an intestinal protozoan that inhabits the intestinal tract of man and other mammals by attaching to the mucosal surface via the contractile activity of an attachment organelle called the ventral adhesive disk. We have investigated the presence of other attachment mechanisms in G. lamblia trophozoites by using microfabricated substrates that sterically interfere with formation of the hypothesized "negative pressure" under the ventral adhesive disk that would mediate attachment to a substratum. Pillars measuring 1 microm high and 2 microm in diam. were constructed in microarrays with spacings smaller than the diameter of the ventral adhesive disk. Using high resolution field emission scanning electron microscopy, the attachment of trophozoites to the tops of pillars in the microfabricated substrates was investigated. Firm adhesion of trophozoites was observed to be mediated by direct attachment of the ventrolateral flange membrane to the tops of microfabricated pillars. Attachment to microfabricated surfaces was 16% of that observed for attachment mediated by the ventral adhesive disk (4.4 +/- 1.5 cells/100 micro2 micropillar surface vs. 25.9 +/- 3.1 cells/100 micro2 flat substrate, p < 0.0001) This is the first report of trophozoite adhesion to a substratum by a mechanism other than the direct attachment of the ventral adhesive disk, and provides experimental evidence that the ventrolateral flange may play a role in trophozoite adhesion. A hypothesis is presented describing how the adhesive nature of the ventrolateral flange might be involved in normal attachment of G. lamblia trophozoites to a substratum.
蓝氏贾第鞭毛虫是一种肠道原生动物,它通过一种名为腹侧黏附盘的附着细胞器的收缩活动附着于黏膜表面,从而栖息在人类和其他哺乳动物的肠道中。我们使用了微制造基板来研究蓝氏贾第鞭毛虫滋养体中其他附着机制的存在,这种基板会在空间上干扰腹侧黏附盘下方假定的“负压”的形成,而这种负压被认为可介导与基质的附着。构建了直径为2微米、高1微米的微阵列柱,其间距小于腹侧黏附盘的直径。使用高分辨率场发射扫描电子显微镜,研究了滋养体在微制造基板上与柱顶的附着情况。观察到滋养体的牢固附着是通过腹外侧边缘膜直接附着于微制造柱顶来介导的。在微制造表面的附着率是腹侧黏附盘介导的附着率的16%(每100平方微米微柱表面有4.4±1.5个细胞,而每100平方微米平面基板上有25.9±3.1个细胞,p<0.0001)。这是关于滋养体通过腹侧黏附盘直接附着以外的机制与基质黏附的首次报道,并提供了实验证据表明腹外侧边缘可能在滋养体黏附中发挥作用。本文提出了一个假说,描述了腹外侧边缘的黏附特性可能如何参与蓝氏贾第鞭毛虫滋养体与基质的正常附着。