Lesniewska E, Giocondi M C, Vié V, Finot E, Goudonnet J P, Le Grimellec C
Centre de Biochimie Structurale, INSERM U414, I.U.R.C., Montpellier, France.
Kidney Int Suppl. 1998 Apr;65:S42-8.
In this brief review, we present three-dimensional images of living Madin-Darby canine kidney (MDCK) cells and CV-1 cells that illustrate the possibilities and limits in the use of atomic force microscopy (AFM) for studying the topography of the cell surfaces and of isolated biological membranes. We show that microvilli can be imaged at the surface of living epithelial cells. However, when these microvilli are abundant and close to each other, the geometry of the AFM tip only allows an access to the upper part of the structures and precludes nanometer range imaging of the cell surface. Such a nanometer range imaging was obtained with other cell types like CV-1 cells and with isolated biological membranes. It reveals that protruding particles 5 to 60 nm xy size, likely corresponding to membranes proteins, occupy most of the membrane surface. These images indicate that the AFM already gives an access to the cell surface structure at the mesoscopic scale, which constitutes a major step for the understanding of the structure-function relationships in membranes. Perspectives for a further step, the imaging at molecular resolution of membranes, are discussed.
在本简要综述中,我们展示了活的麦迪逊-达比犬肾(MDCK)细胞和CV-1细胞的三维图像,这些图像说明了使用原子力显微镜(AFM)研究细胞表面和分离的生物膜形貌的可能性和局限性。我们表明,微绒毛可以在活上皮细胞表面成像。然而,当这些微绒毛丰富且彼此靠近时,AFM尖端的几何形状仅允许接触结构的上部,从而排除了对细胞表面的纳米级成像。这种纳米级成像在其他细胞类型如CV-1细胞和分离的生物膜中获得。结果显示,xy尺寸为5至60 nm的突出颗粒,可能对应于膜蛋白,占据了大部分膜表面。这些图像表明,AFM已经能够在介观尺度上观察细胞表面结构,这是理解膜结构-功能关系的重要一步。本文还讨论了进一步在分子分辨率下对膜进行成像的前景。