INRA, UMR782 Food Process Engineering and Microbiology, F-78850 Thiverval-Grignon, France.
J Microsc. 2012 Jul;247(1):78-93. doi: 10.1111/j.1365-2818.2012.03623.x. Epub 2012 May 21.
In fleshy fruits, the variability of cell morphology at the fruit scale is largely unknown. It presents both a huge variability and a high level of organization. Better knowledge of cell morphology heterogeneity within the fruit is necessary to understand fruit development, to model fruit mechanical behaviour, or to investigate variations of physico-chemical measurements. A generic approach is proposed to build cartographies of cell morphology at the fruit scale, which depict regions corresponding to different cell morphologies. The approach is based on: (1) sampling the whole fruit at known positions; (2) imaging and quantifying local cell morphology; (3) pooling measurements to take biological variability into account and (4) projecting results in a morphology model of the whole fruit. The result is a synthetic representation of cell morphology variations within the whole fruit. The method was applied to the characterization of cell morphology in tomato pericarp. Two different imaging scales that provided complementary descriptions were used: 3D confocal microscopy and macroscopy. The approach is generic and can be adapted to other fruits or other products.
在肉质果实中,果实尺度上细胞形态的可变性在很大程度上是未知的。它具有巨大的可变性和高度的组织性。更好地了解果实内部细胞形态的异质性,对于理解果实发育、模拟果实力学行为或研究物理化学测量的变化是必要的。本文提出了一种通用的方法来构建果实尺度上细胞形态的图谱,该图谱描绘了对应于不同细胞形态的区域。该方法基于:(1)在已知位置对整个果实进行采样;(2)成像和量化局部细胞形态;(3)汇总测量结果,以考虑生物学变异性;(4)将结果投影到整个果实的形态模型中。其结果是整个果实内部细胞形态变化的综合表示。该方法应用于番茄果皮细胞形态的特征描述。使用了两种不同的成像尺度,它们提供了互补的描述:3D 共聚焦显微镜和宏观显微镜。该方法具有通用性,可以适应其他水果或其他产品。