Atomic force microscopy of mammalian urothelial surface

被引:34
|
作者
Kreplak, Laurent
Wang, Huaibin
Aebi, Ueli
Kong, Xiang-Peng
机构
[1] NYU, Sch Med, Dept Biochem, New York, NY 10016 USA
[2] Univ Basel, ME Muller Inst Struct Biol Biozentrum, CH-4056 Basel, Switzerland
关键词
atomic force microscopy; urothelium; tissue; surface; cell junction;
D O I
10.1016/j.jmb.2007.09.040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian urothelium apical surface plays important roles in bladder physiology and diseases, and it provides a unique morphology for ultrastructural studies. Atomic force microscopy (AFM) is an emerging tool for studying the architecture and dynamic properties of biomolecular structures under near-physiological conditions. However, AFM imaging of soft tissues remains a challenge because of the lack of efficient methods for sample stabilization. Using a porous nitrocellulose membrane as the support, we were able to immobilize large pieces of soft mouse bladder tissue, thus enabling us to carry out the first AFM investigation of the mouse urothelial surface. The submicrometer-resolution AFM images revealed many details of the surface features, including the geometry of the urothelial plaques that cover the entire surface and the membrane interdigitation at the cell borders. This interdigitation creates a membrane zipper, likely contributing to the barrier function of the urothelium. In addition, we were able to image the intracellular bacterial communities of type 1-fimbriated bacteria grown between the intermediate filament bundles of the umbrella cells, shedding light on the bacterial colonization of the urothelium. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:365 / 373
页数:9
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