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A novel 2D and 3D method for automated insulin granule measurement and its application in assessing accepted preparation methods for electron microscopy

机译:一种用于自动胰岛素颗粒测量的新型2D和3D方法及其在评估电子显微镜的预接受制备方法中的应用

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Transmission electron microscopy images of insulin-producing beta cells in the islets of Langerhans contain many complex structures, making it difficult to accurately segment insulin granules. Furthermore the appearance of the granules and surrounding halo and limiting membrane can vary enormously depending on the methods used for sample preparation. An automated method has been developed using active contours to segment the insulin core initially and then expand to segment the halos [1]. The method has been validated against manual measurements and also yields higher accuracy than other automated methods [2]. It has then been extended to three dimensions to analyse a tomographic reconstruction from a thick section of the same material. The final step has been to produce a GUI and use the automated process to compare a number of different electron microscopy preparation protocols including chemical fixation (where many of halos are often distended) and to explore the many subtleties of high pressure freezing (where the halos are often minimal, [3]).
机译:在朗格汉兰胰岛中产生胰岛素的β细胞的透射电子显微镜图像含有许多复杂的结构,使得难以准确地分段胰岛素颗粒。此外,颗粒和周围的卤素和限制膜的外观可以根据用于样品制备的方法而变化很大。已经使用活性轮廓开发了一种自动化方法,以便最初将胰岛素核心分段,然后膨胀以分段为HALOS [1]。该方法已针对手动测量验证,并且还产生比其他自动化方法更高的准确性[2]。然后已经扩展到三维,以分析来自相同材料的厚部分的断层切断重建。最后一步是生产GUI,并使用自动化过程比较许多不同的电子显微镜制剂,包括化学固定(其中许多晕晕往往会扩张)并探索高压冷冻的许多微妙之处(其中卤素通常是最小的,[3])。

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