Strausbauch P, Sehgal N
Department of Pathology, School of Medicine, East Carolina University 27858.
J Leukoc Biol. 1989 Nov;46(5):441-9. doi: 10.1002/jlb.46.5.441.
Cells of the beige mouse, the murine counterpart of the Chediak-Higashi Syndrome, contain enlarged anomalous lysosomes. The three-dimensional structure of these lysosomes from peritoneal macrophage was ascertained by study of electron micrographs taken in a series of serial sections combined with computer-assisted analysis. The most common basic structural units identified were biconcave discs and hollow cup/ovoid-shaped structures. Other more bizarre forms were represented by the fusion of these basic lysosomal variants. Anomalous lysosomal forms were found in both beige resident and exudate peritoneal macrophage. A similar study of lysosomes in animals not carrying the beige mutation revealed the presence of smaller but structurally similar forms of the basic lysosomal variants. This latter finding indicates that the presence of lysosomal variants per se in the beige animal is not a finding unique to these animals but rather that their distinctiveness derives from their increased size and propensity to undergo fusion with each other. The usefulness of computer-assisted three-dimensional reconstruction is demonstrated.
米色小鼠是人类切-东综合征(Chediak-Higashi Syndrome)的鼠类对应物,其细胞含有肿大的异常溶酶体。通过对一系列连续切片拍摄的电子显微镜照片进行研究,并结合计算机辅助分析,确定了来自腹膜巨噬细胞的这些溶酶体的三维结构。鉴定出的最常见基本结构单元是双凹圆盘和中空杯状/卵形结构。其他更奇特的形式则由这些基本溶酶体变体的融合表现出来。在米色常驻和渗出性腹膜巨噬细胞中均发现了异常的溶酶体形式。对未携带米色突变的动物的溶酶体进行的类似研究表明,存在较小但结构相似的基本溶酶体变体形式。后一发现表明,米色动物中溶酶体变体的存在本身并非这些动物所特有的发现,而是它们的独特性源于其尺寸增大以及相互融合的倾向。证明了计算机辅助三维重建的实用性。