Maines Mahin D
Department of Biochemistry and Biophysics, University of Rochester Medical Center, New York, USA.
Physiology (Bethesda). 2005 Dec;20:382-9. doi: 10.1152/physiol.00029.2005.
Biliverdin reductase (BVR) functions in cell signaling through three distinct tracks: a dual-specificity kinase that functions in the insulin receptor/MAPK pathways (25, 29, 51); a bzip-type transcription factor for ATF-2/CREB and HO-1 regulation (1, 25); and a reductase that catalyzes the conversion of biliverdin to bilirubin (27). These, together with the protein's primary and secondary features, intimately link BVR to the entire spectrum of cell-signaling cascades.
胆红素还原酶(BVR)通过三条不同途径参与细胞信号传导:一种在胰岛素受体/丝裂原活化蛋白激酶(MAPK)途径中发挥作用的双特异性激酶(25、29、51);一种用于调节ATF-2/CREB和血红素加氧酶-1(HO-1)的碱性亮氨酸拉链(bzip)型转录因子(1、25);以及一种催化胆红素向胆红素转化的还原酶(27)。这些,连同该蛋白的一级和二级特征,将BVR与整个细胞信号级联谱紧密联系起来。