Chang Yong-sheng, Fang Fu-de
National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, CAMS and PUMC, Beijing 100005, China.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2002 Jun;24(3):315-20.
Peroxisome proliferation is a cellular response to many chemical compounds affects including natural and modified fatty acids, phthalate and adipate ester plasticizers, leukotriene antagonists, acetylsalicylic acid and certain pathophysiological conditions including dramatic change of cellular morphology and enzymatic activity. Peroxisome proliferation phenomenon is seen primarily in liver and kidney. Hormones and nutritional factor can regulate peroxisome proliferation response. Sustained peroxisome proliferation can lead to hepatocarcinogenesis. The three types of peroxisome proliferator activated receptor, termed PPAR alpha, PPAR beta, and PPAR gamma, expressed in specific tissue, are consisted of a specific a nuclear receptor superfamily. After more than 10 years world wide research, the function of PPAR is clarified, as PPAR gamma, the master of thrifty genes, controls the expression of genes relative to adipogenesis, diabetes mellitus and obesity. The receptor is involved in transcriptional control of numerous cellular processes including cell cycle control, inflammation, immunoregulation and carcinogenesis.
过氧化物酶体增殖是细胞对许多化合物的一种反应,这些化合物包括天然和改性脂肪酸、邻苯二甲酸酯和己二酸酯增塑剂、白三烯拮抗剂、乙酰水杨酸以及某些病理生理状况,包括细胞形态和酶活性的显著变化。过氧化物酶体增殖现象主要见于肝脏和肾脏。激素和营养因素可调节过氧化物酶体增殖反应。持续的过氧化物酶体增殖可导致肝癌发生。三种类型的过氧化物酶体增殖物激活受体,分别称为PPARα、PPARβ和PPARγ,在特定组织中表达,它们属于一个特定的核受体超家族。经过全球10多年的研究,PPAR的功能已被阐明,作为节俭基因的掌控者,PPARγ控制着与脂肪生成、糖尿病和肥胖相关的基因表达。该受体参与众多细胞过程的转录调控,包括细胞周期控制、炎症、免疫调节和致癌作用。