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胆红素还原酶——阿尔茨海默病和轻度认知障碍患者大脑中的蛋白质水平及活性

Biliverdin reductase--a protein levels and activity in the brains of subjects with Alzheimer disease and mild cognitive impairment.

作者信息

Barone Eugenio, Di Domenico Fabio, Cenini Giovanna, Sultana Rukhsana, Cini Chiara, Preziosi Paolo, Perluigi Marzia, Mancuso Cesare, Butterfield D Allan

机构信息

Department of Chemistry, Center of Membrane Sciences, and Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY 40506-0055, USA.

出版信息

Biochim Biophys Acta. 2011 Apr;1812(4):480-7. doi: 10.1016/j.bbadis.2011.01.005. Epub 2011 Jan 15.

Abstract

Biliverdin reductase-A is a pleiotropic enzyme involved not only in the reduction of biliverdin-IX-alpha into bilirubin-IX-alpha, but also in the regulation of glucose metabolism and cell growth secondary to its serine/threonine/tyrosine kinase activity. Together with heme oxygenase, whose metabolic role is to degrade heme into biliverdin-IX-alpha, it forms a powerful system involved in the cell stress response during neurodegenerative disorders. In this paper, an up-regulation of the biliverdin reductase-A protein levels was found in the hippocampus of the subjects with Alzheimer disease and arguably its earliest form, mild cognitive impairment. Moreover a significant reduction in the phosphorylation of serine, threonine and tyrosine residues of biliverdin reductase-A was found, and this was paralleled by a marked reduction in its reductase activity. Interestingly, the levels of both total and phosphorylated biliverdin reductase-A were unchanged as well as its enzymatic activity in the cerebella. These results demonstrated a dichotomy between biliverdin reductase-A protein levels and activity in the hippocampus of subjects affected by Alzheimer disease and mild cognitive impairment, and this effect likely is attributable to a reduction in the phosphorylation of serine, threonine and tyrosine residues of biliverdin reductase-A. Consequently, not just the increased levels of biliverdin reductase-A, but also its changed activity and phosphorylation state, should be taken into account when considering potential biomarkers for Alzheimer disease and mild cognitive impairment.

摘要

胆绿素还原酶-A是一种多效性酶,不仅参与将胆绿素-IX-α还原为胆红素-IX-α,还因其丝氨酸/苏氨酸/酪氨酸激酶活性参与葡萄糖代谢和细胞生长的调节。它与血红素加氧酶一起,其代谢作用是将血红素降解为胆绿素-IX-α,在神经退行性疾病的细胞应激反应中形成一个强大的系统。在本文中,发现阿尔茨海默病患者以及可以说是其最早形式即轻度认知障碍患者的海马体中胆绿素还原酶-A蛋白水平上调。此外,还发现胆绿素还原酶-A的丝氨酸、苏氨酸和酪氨酸残基磷酸化显著减少,与此同时其还原酶活性也明显降低。有趣的是,小脑内总胆绿素还原酶-A及其磷酸化形式的水平以及其酶活性均未改变。这些结果表明,在受阿尔茨海默病和轻度认知障碍影响的患者海马体中,胆绿素还原酶-A蛋白水平与活性之间存在二分法,这种效应可能归因于胆绿素还原酶-A的丝氨酸、苏氨酸和酪氨酸残基磷酸化减少。因此,在考虑阿尔茨海默病和轻度认知障碍的潜在生物标志物时,不仅应考虑胆绿素还原酶-A水平的升高,还应考虑其活性和磷酸化状态的改变。

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