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Uncoupling protein 2 negatively regulates neurite extensions in PC12h cells.

机译:解偶联蛋白2负调控PC12h细胞中的神经突延伸。

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摘要

Uncoupling protein 2 (UCP2) distributes in many organs including the brain. Though recent reports suggest that UCP2 is involved in the neuroprotection and the regulation of neurosecretion, the roles of UCP2 in the central nervous systems remain largely unclear. In order to clarify the significance of UCP2 in the brain especially at developmental stage, subcellular localizations of rat UCP2 (rUCP2) in the developing cerebellar Purkinje cells were immunochemically examined. The rUCP2-like immunoreactivities observed axon or its terminal during axonal maturation. This result implies that rUCP2 contributes to the neurite development. In the PC12h cells overexpressing rUCP2 or active mutant of rUCP2, the neurite outgrowth was significantly inhibited along with a reduction of cellular ATP level. These findings suggest a possibility that UCP2 is involved in negative regulation of neurite extensions through repression of the energy supply.
机译:解偶联蛋白2(UCP2)分布在包括大脑在内的许多器官中。尽管最近的报道表明UCP2参与了神经保护和神经分泌的调节,但UCP2在中枢神经系统中的作用仍不清楚。为了阐明UCP2在大脑中的重要性,尤其是在发育阶段,我们通过免疫化学方法检查了大鼠UCP2(rUCP2)在发育中的小脑Purkinje细胞中的亚细胞定位。 rUCP2样免疫反应性在轴突成熟过程中观察到轴突或其末端。该结果暗示rUCP2有助于神经突的发展。在过度表达rUCP2或rUCP2的活性突变体的PC12h细胞中,神经突的生长被显着抑制,同时细胞ATP水平降低。这些发现表明,UCP2可能通过抑制能量供应而参与神经突延伸的负调控。

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