De Craemer D, Pauwels M, Hautekeete M, Roels F
Department of Human Anatomy and Embryology, Vrije Universiteit Brussel, Belgium.
Cancer. 1993 Jun 15;71(12):3851-8. doi: 10.1002/1097-0142(19930615)71:12<3851::aid-cncr2820711210>3.0.co;2-l.
Hepatic catalase activity is decreased in patients with malignant diseases, but little is known about the organelles that contain the bulk of catalase: the peroxisomes.
The authors studied the hepatocellular peroxisomes in patients with malignant diseases by means of catalase cytochemistry, light and electron microscopic study, and morphometry.
Under the light microscope, a decrease in catalase staining was observed in 21 of 39 patients with extrahepatic tumors. A peculiar perinuclear concentration of peroxisomes was seen by light microscopic study in 15 of 39 patients and reflected an increase in number in most patients. In one of two hepatoma livers, peroxisomes also showed this perinuclear configuration. Ultrastructural and morphometric analysis of 20 livers of patients with extrahepatic tumors revealed a decreased mean peroxisomal diameter and an increase in number. Electron microscopic study also showed peroxisomes with transparent matrical spots, cytoplasmic invaginations, protrusions, and gastruloid cisternae. In each liver, at least one of these changes was observed. In hepatoma livers, one-third of the peroxisomes revealed empty matrical spots. In one patient, peroxisomes were smaller but more numerous.
Alterations of the peroxisomal compartment are constant findings in the livers of patients with malignant diseases, but individual differences in peroxisomal alterations are frequent.
恶性疾病患者肝脏过氧化氢酶活性降低,但对于含有大部分过氧化氢酶的细胞器——过氧化物酶体,人们了解甚少。
作者通过过氧化氢酶细胞化学、光镜和电镜研究以及形态计量学方法,对恶性疾病患者的肝细胞过氧化物酶体进行了研究。
在光镜下,39例肝外肿瘤患者中有21例过氧化氢酶染色减少。光镜研究发现,39例患者中有15例过氧化物酶体出现核周特殊聚集,且多数患者过氧化物酶体数量增加。在2例肝癌肝脏中,有1例过氧化物酶体也呈现这种核周形态。对20例肝外肿瘤患者的肝脏进行超微结构和形态计量分析发现,过氧化物酶体平均直径减小,数量增加。电镜研究还显示过氧化物酶体出现透明基质斑、胞质内陷、突起和胃小凹样池。在每例肝脏中,至少观察到上述一种变化。在肝癌肝脏中,三分之一的过氧化物酶体显示基质斑为空泡状。有1例患者,过氧化物酶体较小但数量较多。
过氧化物酶体区室改变是恶性疾病患者肝脏的常见表现,但过氧化物酶体改变存在个体差异。