Silva R F, Mata L M, Gulbenkian S, Brites D
Centro de Patogénese Molecular, Faculdade de Farmácia, University of Lisbon, Portugal.
Neurochem Res. 2001 Jul;26(7):793-800. doi: 10.1023/a:1011608017870.
Excessive hyperbilirubinemia can cause irreversible neurological damage in the neonatal period. However, the complete understanding of the pathogenesis of unconjugated bilirubin (UCB) encephalopathy remains a matter of debate. This study investigates whether UCB inhibits the endocytosis of cationized ferritin (CF) by cultured rat astrocytes. The relationship between endocytosis and MTT reduction, as well as changes on tubulin and glial fibrillary acidic protein (GFAP) assembly, were also evaluated. Inhibition of endocytosis was complete in the presence of 171 microM UCB, while a marked decrease of CF labeling was noticed for 86 microM UCB. In addition, MTT reduction was inhibited by 60 to 76% as UCB concentrations changed from 17 to 171 microM, while alterations on both GFAP and microtubule morphology were only achieved by cell exposure to 171 microM UCB. These findings indicate that inhibition of CF endocytosis in rat cortical astrocytes by UCB is a concentration-dependent process that appears to be primarily related to a direct effect on the cell membrane and not to any alteration of cytoskeletal microtubules and intermediate filaments.
新生儿期过高的高胆红素血症可导致不可逆的神经损伤。然而,对未结合胆红素(UCB)脑病发病机制的全面理解仍存在争议。本研究调查UCB是否抑制培养的大鼠星形胶质细胞对阳离子铁蛋白(CF)的内吞作用。还评估了内吞作用与MTT还原之间的关系,以及微管蛋白和胶质纤维酸性蛋白(GFAP)组装的变化。在存在171微摩尔UCB的情况下,内吞作用完全受到抑制,而对于86微摩尔UCB,CF标记明显减少。此外,随着UCB浓度从17微摩尔变化到171微摩尔,MTT还原受到60%至76%的抑制,而只有细胞暴露于171微摩尔UCB时,GFAP和微管形态才会发生改变。这些发现表明,UCB对大鼠皮质星形胶质细胞CF内吞作用的抑制是一个浓度依赖性过程,这似乎主要与对细胞膜的直接作用有关,而与细胞骨架微管和中间丝的任何改变无关。