Unit of Cardiac Physiology, School of Biomedicine, The University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9PT, UK.
Matrix Biol. 2010 May;29(4):254-60. doi: 10.1016/j.matbio.2010.01.008. Epub 2010 Feb 6.
Conventional approaches for ultrastructural high-resolution imaging of biological specimens induce profound changes in bio-molecular structures. By combining tissue cryo-sectioning with non-destructive atomic force microscopy (AFM) imaging we have developed a methodology that may be applied by the non-specialist to both preserve and visualize bio-molecular structures (in particular extracellular matrix assemblies) in situ. This tissue section AFM technique is capable of: i) resolving nm-microm scale features of intra- and extracellular structures in tissue cryo-sections; ii) imaging the same tissue region before and after experimental interventions; iii) combining ultrastructural imaging with complimentary microscopical and micromechanical methods. Here, we employ this technique to: i) visualize the macro-molecular structures of unstained and unfixed fibrillar collagens (in skin, cartilage and intervertebral disc), elastic fibres (in aorta and lung), desmosomes (in nasal epithelium) and mitochondria (in heart); ii) quantify the ultrastructural effects of sequential collagenase digestion on a single elastic fibre; iii) correlate optical (auto fluorescent) with ultrastructural (AFM) images of aortic elastic lamellae.
传统的生物标本超微结构高分辨率成像方法会导致生物分子结构发生深刻变化。通过将组织冷冻切片与无损原子力显微镜(AFM)成像相结合,我们开发了一种方法,即使是非专业人员也可以应用该方法原位保存和可视化生物分子结构(特别是细胞外基质组装)。这种组织切片 AFM 技术能够:i)解析组织冷冻切片中细胞内和细胞外结构的纳米到微米尺度特征;ii)在实验干预前后对同一组织区域进行成像;iii)将超微结构成像与互补的显微镜和微力学方法相结合。在这里,我们将该技术用于:i)可视化未染色和未固定的纤维状胶原蛋白(在皮肤、软骨和椎间盘)、弹性纤维(在主动脉和肺)、桥粒(在鼻上皮)和线粒体(在心脏)的宏观分子结构;ii)定量分析胶原酶消化对单个弹性纤维的超微结构影响;iii)对主动脉弹性小梁板的光学(自发荧光)与超微结构(AFM)图像进行相关分析。