Fan C Y, Pan J, Chu R, Lee D, Kluckman K D, Usuda N, Singh I, Yeldandi A V, Rao M S, Maeda N, Reddy J K
Department of Pathology, Northwestern University Medical School, Chicago, Illinois 60611, USA.
J Biol Chem. 1996 Oct 4;271(40):24698-710. doi: 10.1074/jbc.271.40.24698.
Peroxisomal genetic disorders, such as Zellweger syndrome, are characterized by defects in one or more enzymes involved in the peroxisomal beta-oxidation of very long chain fatty acids and are associated with defective peroxisomal biogenesis. The biologic role of peroxisomal beta-oxidation system, which consists of three enzymes: fatty acyl-CoA oxidase (ACOX), enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase (HD), and thiolase, has been examined in mice by disrupting ACOX gene, which encodes the first and rate-limiting enzyme of this system. Homozygous (ACOX -/-) mice lacked the expression of ACOX protein and accumulate very long chain fatty acids in blood. However, these homozygous mice are viable, but growth-retarded and infertile. During the first 3-4 months of age, the livers of ACOX -/- mice reveal severe microvesicular fatty metamorphosis of hepatocytes. In such steatotic cells, peroxisome assembly is markedly defective; as a result, they contain few or no peroxisomes. Few hepatocytes in 1-3-month-old ACOX -/- mice contain numerous peroxisomes, and these peroxisome-rich hepatocytes show no fatty change. At this stage, the basal mRNA levels of HD, thiolase, and other peroxisome proliferator-induced target genes were elevated in ACOX -/- mouse liver, but these mice, when treated with a peroxisome proliferator, showed no increases in the number of hepatic peroxisomes and in the mRNAs levels of these target genes. Between 4 and 5 months of age, severe steatosis resulted in scattered cell death, steatohepatitis, formation of lipogranulomas, and focal hepatocellular regeneration. In 6-7-month-old animals, the newly emerging hepatocytes, which progressively replaced steatotic cells, revealed spontaneous peroxisome proliferation. These livers showed marked increases in the mRNA levels of the remaining two genes of the beta-oxidation system, suggesting that ACOX gene disruption leads to increased endogenous ligand-mediated transcription levels. These observations demonstrate links among peroxisomal beta-oxidation, development of severe microvesicular fatty liver, peroxisome assembly, cell death, and cell proliferation in liver.
过氧化物酶体遗传疾病,如泽尔韦格综合征,其特征是参与极长链脂肪酸过氧化物酶体β-氧化的一种或多种酶存在缺陷,并与过氧化物酶体生物发生缺陷有关。过氧化物酶体β-氧化系统由三种酶组成:脂肪酰辅酶A氧化酶(ACOX)、烯酰辅酶A水合酶/3-羟酰基辅酶A脱氢酶(HD)和硫解酶,通过破坏编码该系统第一种也是限速酶的ACOX基因,在小鼠中研究了该系统的生物学作用。纯合子(ACOX -/-)小鼠缺乏ACOX蛋白的表达,血液中积累极长链脂肪酸。然而,这些纯合子小鼠是存活的,但生长发育迟缓且不育。在1至3个月大时,ACOX -/-小鼠的肝脏显示肝细胞严重微泡性脂肪变性。在这种脂肪变性细胞中,过氧化物酶体组装明显存在缺陷;因此,它们含有很少或没有过氧化物酶体。1至3个月大的ACOX -/-小鼠中很少有肝细胞含有大量过氧化物酶体,这些富含过氧化物酶体的肝细胞没有脂肪变化。在此阶段,ACOX -/-小鼠肝脏中HD、硫解酶和其他过氧化物酶体增殖物诱导的靶基因的基础mRNA水平升高,但这些小鼠在用过氧化物酶体增殖物处理时,肝脏过氧化物酶体数量和这些靶基因的mRNA水平没有增加。在4至5个月大时,严重的脂肪变性导致散在的细胞死亡、脂肪性肝炎、脂肉芽肿形成和局灶性肝细胞再生。在6至7个月大的动物中,逐渐取代脂肪变性细胞的新出现的肝细胞显示出自发性过氧化物酶体增殖。这些肝脏中β-氧化系统其余两个基因的mRNA水平显著增加,表明ACOX基因破坏导致内源性配体介导的转录水平升高。这些研究结果证明了过氧化物酶体β-氧化、严重微泡性脂肪肝的发展、过氧化物酶体组装、细胞死亡和肝脏细胞增殖之间的联系。