Adhesion forces and mechanics in mannose-mediated acanthamoeba interactions

被引:14
|
作者
Huth, Steven [1 ]
Reverey, Julia F. [1 ]
Leippe, Matthias [2 ]
Selhuber-Unkel, Christine [1 ]
机构
[1] Christian Albrecht Univ Kiel, Inst Mat Sci Biocompatible Nanomat, Kaiserstr 2, D-24143 Kiel, Germany
[2] Christian Albrecht Univ Kiel, Zool Inst, Comparat Immunobiol, Botanischen Garten 1-9, D-24118 Kiel, Germany
来源
PLOS ONE | 2017年 / 12卷 / 05期
基金
欧洲研究理事会;
关键词
BINDING PROTEIN; CELL-ADHESION; IN-VITRO; PATHOGENIC ACANTHAMOEBA; CONTACT-LENSES; KERATITIS; CASTELLANII; DISEASE; AMEBAS; SOFT;
D O I
10.1371/journal.pone.0176207
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The human pathogenic amoeba Acanthamoeba castellanii (A. castellanii) causes severe diseases, including acanthamoeba keratitis and encephalitis. Pathogenicity arises from the killing of target-cells by an extracellular killing mechanism, where the crucial first step is the formation of a close contact between A. castellanii and the target-cell. This process is mediated by the glycocalix of the target-cell and mannose has been identified as key mediator. The aim of the present study was to carry out a detailed biophysical investigation of mannose-mediated adhesion of A. castellanii using force spectroscopy on single trophozoites. In detail, we studied the interaction of a mannose-coated cantilever with an A. castellanii trophozoite, as mannose is the decisive part of the cellular glycocalix in mediating pathogenicity. We observed a clear increase of the force to initiate cantilever detachment from the trophozoite with increasing contact time. This increase is also associated with an increase in the work of detachment. Furthermore, we also analyzed single rupture events during the detachment process and found that single rupture processes are associated with membrane tether formation, suggesting that the cytoskeleton is not involved in mannose binding events during the first few seconds of contact. Our study provides an experimental and conceptual basis for measuring interactions between pathogens and target-cells at different levels of complexity and as a function of interaction time, thus leading to new insights into the biophysical mechanisms of parasite pathogenicity.
引用
收藏
页数:14
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