Odin P, Obrink B
Department of Neurology, University Hospital, Lund, Sweden.
Exp Cell Res. 1988 Nov;179(1):89-103. doi: 10.1016/0014-4827(88)90351-5.
In the present investigation we have used a sensitive immunohistochemical technique to study the appearance and cell-surface distribution of cellCAM 105 in rat fetal tissues and in regenerating liver. CellCAM 105 is an integral membrane glycoprotein that is involved in cell-cell adhesion of mature rat hepatocytes in vitro. In 12-day-old rat fetuses no cellCAM 105 was detected. CellCAM 105 then appeared on Day 13 in megakaryocytes of the fetal liver, on Day 16 in the liver parenchyme, and on Day 17 in the epithelial cells of the proximal kidney tubules and of the small intestinal mucosa. In the liver parenchyme cellCAM 105 first appeared in immature bile canaliculi. During Days 19-21 a significant staining also occurred on the contiguous sides of the hepatocytes, which at that time became closely associated when the blood-forming cells disappeared. This surface staining then gradually disappeared and 2-3 weeks after birth cellCAM 105 was expressed in the bile canalicular area which is typical of mature hepatocytes. In regenerating liver the amount of cellCAM 105 decreases to a minimum 2-3 days post-hepatectomy, then increases and reaches the normal concentration 10-15 days post-hepatectomy [Odin and Obrink (1986) Exp. Cell Res. 164, 103-114]. The cell-surface distribution of cellCAM 105 also changed, and on Days 3-5 post-hepatectomy it appeared on all faces of the hepatocytes which then were closely associated without obvious sinusoids in between. This staining pattern then slowly changed toward the normal pattern of mature liver, which appeared about 15 days post-hepatectomy. A theoretical analysis of the mode of hepatocyte cell division during liver regeneration suggested that the surface of the postmitotic hepatocytes should become unpolarized with respect to macromolecular composition. This is in agreement with the observed surface distribution of cellCAM 105. The results support the hypothesis that cell-surface interactions mediated by cellCAM 105 might contribute to the regular organization of hepatocytes in the normal, mature liver plates.
在本研究中,我们采用了一种灵敏的免疫组织化学技术,来研究细胞黏附分子105(CellCAM 105)在大鼠胎儿组织和再生肝脏中的出现情况及细胞表面分布。CellCAM 105是一种整合膜糖蛋白,在体外参与成熟大鼠肝细胞的细胞间黏附。在12日龄的大鼠胎儿中未检测到CellCAM 105。CellCAM 105随后在第13天出现在胎儿肝脏的巨核细胞中,在第16天出现在肝实质中,在第17天出现在近端肾小管和小肠黏膜的上皮细胞中。在肝实质中,CellCAM 105首先出现在未成熟的胆小管中。在第19 - 21天期间,肝细胞相邻面也出现明显染色,此时造血细胞消失,肝细胞紧密相连。这种表面染色随后逐渐消失,出生后2 - 3周,CellCAM 105在成熟肝细胞典型的胆小管区域表达。在再生肝脏中,肝切除术后2 - 3天,CellCAM 105的量降至最低,然后增加,在肝切除术后10 - 15天达到正常浓度[奥丁和奥布林克(1986年)《实验细胞研究》164卷,第103 - 114页]。CellCAM 105的细胞表面分布也发生了变化,肝切除术后第3 - 5天,它出现在肝细胞的所有表面,此时肝细胞紧密相连,其间无明显的肝血窦。这种染色模式随后缓慢转变为成熟肝脏的正常模式,该模式在肝切除术后约15天出现。对肝脏再生过程中肝细胞分裂方式的理论分析表明,有丝分裂后肝细胞的表面在大分子组成方面应变为非极化状态。这与观察到的CellCAM 105的表面分布情况相符。这些结果支持了这样一种假说,即由CellCAM 105介导的细胞表面相互作用可能有助于正常成熟肝板中肝细胞的规则排列。