Kukoba T V, Moĭbenko O O
A.A. Bogomoletz Institute of Physiology, National Academy of Sciences of Ukraine, Kiyv.
Fiziol Zh (1994). 2002;48(5):79-92.
Heme oxygenase (HO) catalyzes the conversion of heme to carbon monoxide, iron, and biliverdin, which is immediately reduced to bilirubin. Three HO active isozymes exist: HO-1, an inducible heat shock protein (HSP32), and HO-2 and HO-3, which are constitutive and highly concentrated in neurons, spleen and liver. Heme oxygenase-1 is an inducible enzyme that catalyzes heme degradation and has been proposed to play a role in protecting cells against oxidative stress-related injury. The mechanism(s) of protection is not completely elucidated, although it is suggested that one or more of the catalytic by-products provide antioxidant functions either directly or indirectly. The role played by heme oxygenase in tissue pathology is determined by a delicate balance between the injurious and protective actions of heme, bilirubin, CO, and Fe2+. Authors review the functional role of HO and its derivates in cells biology and its real potential application to pathological conditions.
血红素加氧酶(HO)催化血红素转化为一氧化碳、铁和胆绿素,胆绿素随即被还原为胆红素。存在三种HO活性同工酶:HO-1,一种可诱导的热休克蛋白(HSP32),以及HO-2和HO-3,它们是组成型的,在神经元、脾脏和肝脏中高度富集。血红素加氧酶-1是一种可诱导的酶,催化血红素降解,有人提出它在保护细胞免受氧化应激相关损伤中发挥作用。尽管有人认为一种或多种催化副产物直接或间接提供抗氧化功能,但保护机制尚未完全阐明。血红素加氧酶在组织病理学中所起的作用取决于血红素、胆红素、一氧化碳和Fe2+的损伤作用与保护作用之间的微妙平衡。作者综述了HO及其衍生物在细胞生物学中的功能作用及其在病理状况下的实际潜在应用。