Gorgas K
Anat Embryol (Berl). 1984;169(3):261-70. doi: 10.1007/BF00315631.
The ultrastructure of peroxisomes in partially differentiated cells of the mouse preputial gland was investigated using serial thin sections and three-dimensional reconstruction as well as the alkaline diaminobenzidine technique for visualization of the peroxidatic activity of catalase. An analysis of serial sections indicates that the different types of intensely stained peroxisomal profiles, classified according to their shape, represent random planes through highly complex peroxisomes. These organelles exceed 4 micron in length and exhibit a focal heterogeneity with respect to their size, shape and enzyme distribution. The graphical three-dimensional reconstruction demonstrates that the most intricate peroxisomes are characterized by tortuous, elongate, and branched tubular segments of varying diameter equipped with enlarged terminal hollow-spherical structures which engulf areas of cytoplasm. A close spatial relationship is established between adjacent peroxisomes and peroxisomes and mitochondria, the latter two of which synchronously develop into highly complex structures. A close association is also observed between peroxisomes and the endoplasmic reticulum, whereby membrane continuities between the two compartments cannot be demonstrated. These observations are inconsistent with traditional concepts concerning peroxisomal shape and size, the number per cell, as well as their biogenesis from the endoplasmic reticulum. The functional significance of individual highly complex peroxisomes and their assemblage forming an extensive net-like membraneous system throughout the cell is discussed with respect to intracellular energy transport and transmembrane electron exchange.
利用连续超薄切片、三维重建以及碱性二氨基联苯胺技术对过氧化氢酶的过氧化物活性进行可视化,研究了小鼠包皮腺部分分化细胞中过氧化物酶体的超微结构。对连续切片的分析表明,根据形状分类的不同类型的深染过氧化物酶体轮廓代表了通过高度复杂的过氧化物酶体的随机平面。这些细胞器长度超过4微米,在大小、形状和酶分布方面表现出局部异质性。图形三维重建表明,最复杂的过氧化物酶体的特征是具有不同直径的曲折、细长和分支的管状部分,并配备有扩大的末端空心球形结构,这些结构吞噬细胞质区域。相邻的过氧化物酶体与过氧化物酶体和线粒体之间建立了紧密的空间关系,后两者同步发育成高度复杂的结构。在过氧化物酶体与内质网之间也观察到密切的联系,然而,无法证明这两个区室之间的膜连续性。这些观察结果与关于过氧化物酶体形状和大小、每个细胞中的数量以及它们由内质网产生的传统概念不一致。关于细胞内能量运输和跨膜电子交换,讨论了单个高度复杂的过氧化物酶体及其组装形成贯穿整个细胞的广泛的网状膜系统的功能意义。