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LOX-1在HN33神经元细胞系中的表达、氧化型低密度脂蛋白摄取及毒性

LOX-1 expression and oxidized LDL uptake and toxicity in the HN33 neuronal cell line.

作者信息

Mao Xiaoou, Xie Lin, Greenberg David A

机构信息

Buck Institute for Research on Aging, 8001 Redwood Boulevard, Novato, CA 94945, USA.

Buck Institute for Research on Aging, 8001 Redwood Boulevard, Novato, CA 94945, USA.

出版信息

Neurosci Lett. 2014 Sep 19;580:182-5. doi: 10.1016/j.neulet.2014.03.061. Epub 2014 Apr 3.

Abstract

Cardiovascular risk factors appear to influence the risk and progression of neurodegenerative disease, but the mechanisms involved are poorly understood. We investigated the possible involvement of oxidized low-density lipoprotein receptor (LOX-1) and oxidized low-density lipoprotein (Ox-LDL) in neurodegeneration by studying the expression of LOX-1 and the effects of Ox-LDL in HN33 cells, a neuronal cell line of central nervous system origin. HN33 cells showed LOX-1 protein expression, hypoxic induction of LOX-1, Ox-LDL uptake and Ox-LDL toxicity. LOX-1/Ox-LDL signaling may contribute to the association between cardiovascular risk factors and neurodegenerative disease.

摘要

心血管危险因素似乎会影响神经退行性疾病的风险和进展,但其涉及的机制却知之甚少。我们通过研究氧化型低密度脂蛋白受体(LOX-1)的表达以及氧化型低密度脂蛋白(Ox-LDL)对HN33细胞(一种源自中枢神经系统的神经元细胞系)的影响,来探究LOX-1和Ox-LDL在神经退行性变中的可能作用。HN33细胞表现出LOX-1蛋白表达、LOX-1的低氧诱导、Ox-LDL摄取以及Ox-LDL毒性。LOX-1/Ox-LDL信号传导可能促成了心血管危险因素与神经退行性疾病之间的关联。

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