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血清中骨形态发生蛋白-2(BMP-2)水平升高与骨形态发生蛋白-4(BMP-4)和骨形态发生蛋白-5(BMP-5)水平相关,并导致复发缓解型多发性硬化症患者的神经元表型减少。

High serum levels of BMP-2 correlate with BMP-4 and BMP-5 levels and induce reduced neuronal phenotype in patients with relapsing-remitting multiple sclerosis.

作者信息

Penn Moran, Mausner-Fainberg Karin, Golan Maya, Karni Arnon

机构信息

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Neuroimmunology Laboratory, Department of Neurology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

出版信息

J Neuroimmunol. 2017 Sep 15;310:120-128. doi: 10.1016/j.jneuroim.2017.07.008. Epub 2017 Jul 15.

Abstract

Blockage of bone morphogenetic protein (BMP) signaling is required for differentiation of neurons and oligodendrocytes from neural stem cells (NSCs). Sera of untreated relapsing-remitting multiple sclerosis (RR-MS) patients expressed significantly higher levels of BMP-2 compared to sera of healthy controls. BMP-2 levels correlated with BMP-4 and -5 levels only in sera of untreated MS patients. Furthermore, sera of untreated patients inhibited the neuronal differentiation of RA-treated P19 cells, which was associated with induction of phospho-SMAD signaling pathway. These results suggest that BMP-2 sera levels may play a role in the failure of remyelination and neuro-regeneration in RR-MS.

摘要

神经干细胞(NSCs)分化为神经元和少突胶质细胞需要阻断骨形态发生蛋白(BMP)信号传导。与健康对照者的血清相比,未经治疗的复发缓解型多发性硬化症(RR-MS)患者的血清中BMP-2水平显著更高。仅在未经治疗的MS患者血清中,BMP-2水平与BMP-4和-5水平相关。此外,未经治疗患者的血清抑制了视黄酸(RA)处理的P19细胞的神经元分化,这与磷酸化SMAD信号通路的诱导有关。这些结果表明,BMP-2血清水平可能在RR-MS的髓鞘再生和神经再生失败中起作用。

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