Rybicka K K
Department of Physiology, State University of New York, Buffalo 14214, USA.
Tissue Cell. 1996 Jun;28(3):253-65. doi: 10.1016/s0040-8166(96)80013-9.
This article reviews the data concerning the electron microscopical interpretation of glycogen. It demonstrates that glycogen in the cell is associated with the enzymes involved in its metabolism and that the glycogen-protein complex forms morphologically distinct cell organelles called glycosomes. Glycogen can be visualized in the electron microscope (EM) by histochemical procedures, or by negative staining, but it does not react with heavy metals such as uranium and lead. The protein component of glycosomes, stainable by heavy metals, appears in EM as 20-30 nm granules. While biochemical findings have long indicated the association of glycogen and protein in the cell, morphological interpretation traditionally defined the protein component of glycosomes as particles of glycogen. Accordingly, the term alpha or beta particles, introduced to define particles of glycogen, became subsequently applied to the protein component visible in sections stained by heavy metals. The history of microscopic research reveals the conditions which led to such interpretation. Morphological analysis of the reaction of glycosomes to the acids shows that glycosomes deposited free in the cytosol (lyoglycosomes) are acid labile, whereas the others (desmoglycosomes), intimately associated with different cellular structures, are acid-resistant. These 2 groups correspond to lyo- and desmoglycogen distinguished in early biochemical studies on the basis of their different resistance to the cold trichloroacetic acid. The theory of glycosomes provides a new paradigm which clarifies numerous unexplained data in the microscopic literature on glycogen, and opens a vast field for the research on the cellular metabolism of glycogen, with the use of modern molecular and cellular biology techniques.
本文综述了有关糖原的电子显微镜解释的数据。它表明细胞中的糖原与参与其代谢的酶相关联,并且糖原 - 蛋白质复合物形成形态上不同的细胞器,称为糖原粒。糖原可以通过组织化学方法或负染色在电子显微镜(EM)中可视化,但它不与铀和铅等重金属发生反应。糖原粒的蛋白质成分可被重金属染色,在电子显微镜下呈现为20 - 30纳米的颗粒。虽然生化研究结果长期以来表明细胞中糖原与蛋白质有关联,但传统的形态学解释将糖原粒的蛋白质成分定义为糖原颗粒。因此,最初用于定义糖原颗粒的α或β颗粒这一术语,随后被应用于在重金属染色切片中可见的蛋白质成分。微观研究的历史揭示了导致这种解释的条件。对糖原粒与酸反应的形态学分析表明,游离沉积在细胞质溶胶中的糖原粒(溶糖原粒)对酸不稳定,而其他与不同细胞结构紧密相关的糖原粒(结合糖原粒)则耐酸。这两组对应于早期生化研究中根据对冷三氯乙酸的不同抗性而区分的溶糖原和结合糖原。糖原粒理论提供了一种新的范式,它澄清了关于糖原的微观文献中许多无法解释的数据,并利用现代分子和细胞生物学技术为糖原的细胞代谢研究开辟了广阔的领域。