Oikawa I, Novikoff P M
Department of Pathology, Albert Einstein College of Medicine, Bronx, New York 10461.
Am J Pathol. 1995 Mar;146(3):673-87.
Using light microscopy enzyme cytochemistry to localize catalase activity in peroxisomes, a population of peroxisome-negative hepatocytes was detected in livers of rats during liver regeneration induced by two-thirds partial hepatectomy. However, examination by electron microscopy revealed that this population of hepatocytes contained peroxisomes with a delimiting membrane and a nucleoid, but no cytochemically demonstrable catalase activity within their matrix. Regenerating livers 6, 18, 24, 36, 48 and 72 hours, and 1 week after partial hepatectomy showed hepatocytes without catalase activity. However, their numbers varied, with the most numerous appearing at 24 hours after partial hepatectomy. Mitosis of catalase-negative hepatocytes were seen along with mitosis of hepatocytes containing the normal complement of catalase-positive peroxisomes. The catalase-negative hepatocytes did not show evidence of apoptosis or necrotic cell death. Lysosomal acid phosphatase activity and bile canalicular ATPase activity were present in hepatocytes with catalase-negative peroxisomes. Another population of hepatocytes with a small number of catalase-positive peroxisomes appeared and were more numerous at 36 hours after partial hepatectomy; ultrastructurally, these hepatocytes contained both catalase-negative peroxisomes, which appeared to undergo dissolution, and catalase-positive peroxisomes, which were smaller in size. After complete restoration of the liver, all hepatocytes displayed essentially uniform numbers of catalase-positive peroxisomes. These studies indicated that during liver regeneration there is a transient loss of catalase in peroxisomes of some hepatocytes. These cells proliferate and with time acquire new catalase-positive peroxisomes. The observations are discussed in relation to peroxisome biogenesis, hepatocellular carcinogenesis, and oxidative stress during liver regeneration.
利用光学显微镜酶细胞化学技术对过氧化物酶体中的过氧化氢酶活性进行定位,在三分之二肝部分切除诱导的大鼠肝再生过程中,肝脏中检测到一群过氧化物酶体阴性的肝细胞。然而,电子显微镜检查显示,这群肝细胞含有具有界膜和拟核的过氧化物酶体,但其基质内没有细胞化学可证实的过氧化氢酶活性。部分肝切除术后6、18、24、36、48和72小时以及1周的再生肝脏显示出无过氧化氢酶活性的肝细胞。然而,它们的数量各不相同,在部分肝切除术后24小时出现的数量最多。可见过氧化氢酶阴性肝细胞的有丝分裂以及含有正常数量过氧化氢酶阳性过氧化物酶体的肝细胞的有丝分裂。过氧化氢酶阴性肝细胞未显示凋亡或坏死性细胞死亡的迹象。过氧化氢酶阴性过氧化物酶体的肝细胞中存在溶酶体酸性磷酸酶活性和胆小管ATP酶活性。另一群含有少量过氧化氢酶阳性过氧化物酶体的肝细胞出现,在部分肝切除术后36小时数量更多;超微结构上看,这些肝细胞既含有似乎正在溶解的过氧化氢酶阴性过氧化物酶体,也含有体积较小的过氧化氢酶阳性过氧化物酶体。肝脏完全恢复后,所有肝细胞显示出基本均匀数量的过氧化氢酶阳性过氧化物酶体。这些研究表明,在肝再生过程中,一些肝细胞的过氧化物酶体中过氧化氢酶会短暂缺失。这些细胞增殖并随着时间获得新的过氧化氢酶阳性过氧化物酶体。结合过氧化物酶体生物发生、肝细胞癌发生以及肝再生过程中的氧化应激对这些观察结果进行了讨论。