Araki N, Ohno J, Lee T, Takashima Y, Ogawa K
Department of Anatomy, Ehime University School of Medicine, Japan.
Exp Cell Res. 1993 Feb;204(2):181-91. doi: 10.1006/excr.1993.1023.
The distribution of lysosomes in rat hepatocytes was examined by three-dimensional electron microscopy combined with acid phosphatase (ACPase) cytochemistry. In the 2-microns-thick sections observed under 200- or 1000-kV TEM, it was apparent that ACPase activity localized on elongate lysosomes (we refer to them as nematolysosomes) with a diameter of 70-100 nm and lengths of several micrometers, as well as spherical lysosomes and trans-Golgi cisternae. Though most spherical lysosomes were located within the pericanalicular region, nematolysosomes were widely distributed throughout the hepatocytes. Typically, it appeared that the nematolysosomes elongated from the subsinusoidal region to the pericanalicular-Golgi complex area and they frequently formed a network at the cell periphery along the sinusoidal front. Furthermore, the formation of nematolysosomes was independent of new protein synthesis, but highly dependent on the integrity of microtubules. After a 6-8 h colchicine treatment, nematolysosomes were shrunk and/or fragmented, becoming roughly spherical lysosomes scattered throughout the cells. Nematolysosomes recovered their normal profiles after 24 h due to the reversible effect of the drug on microtubules. When the hepatocytes were exposed to horseradish peroxidase (HRP) in vitro or in vivo, HRP was quickly sequestered in nematolysosome-like structures via pinocytosis from the sinusoidal surface and transported to an area near the Golgi complex. These findings raise the possibility that the nematolysosomes engage in microtubule-dependent transport of macromolecules from the sinusoidal circulation to the Golgi complex area.
通过三维电子显微镜结合酸性磷酸酶(ACPase)细胞化学方法,研究了大鼠肝细胞中溶酶体的分布情况。在200千伏或1000千伏透射电子显微镜下观察的2微米厚切片中,明显可见ACPase活性定位于直径70 - 100纳米、长度为几微米的细长型溶酶体(我们将其称为线虫状溶酶体),以及球形溶酶体和反式高尔基体潴泡。虽然大多数球形溶酶体位于胆小管周围区域,但线虫状溶酶体广泛分布于整个肝细胞中。通常情况下,线虫状溶酶体从窦周区域延伸至胆小管 - 高尔基体复合体区域,并且它们经常在细胞周边沿着窦状前沿形成网络。此外,线虫状溶酶体的形成不依赖于新的蛋白质合成,但高度依赖于微管的完整性。用秋水仙碱处理6 - 8小时后,线虫状溶酶体收缩和/或碎片化,变成大致球形的溶酶体散布于整个细胞中。由于药物对微管的可逆作用,24小时后线虫状溶酶体恢复其正常形态。当肝细胞在体外或体内暴露于辣根过氧化物酶(HRP)时,HRP通过从窦状表面的胞饮作用迅速被隔离在线虫状溶酶体样结构中,并被运输到高尔基体复合体附近的区域。这些发现增加了线虫状溶酶体参与从窦状循环到高尔基体复合体区域的大分子微管依赖性运输的可能性。