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少突胶质细胞中SHP-1对活性氧产生的调控。

The control of reactive oxygen species production by SHP-1 in oligodendrocytes.

作者信息

Gruber Ross C, LaRocca Daria, Minchenberg Scott B, Christophi George P, Hudson Chad A, Ray Alex K, Shafit-Zagardo Bridget, Massa Paul T

机构信息

Department of Neurology, SUNY Upstate Medical University, Syracuse, New York.

Department of Pathology, Albert Einstein College of Medicine, Bronx, New York.

出版信息

Glia. 2015 Oct;63(10):1753-71. doi: 10.1002/glia.22842. Epub 2015 Apr 27.

Abstract

We have previously described reduced myelination and corresponding myelin basic protein (MBP) expression in the central nervous system of Src homology 2 domain-containing protein tyrosine phosphatase 1 (SHP-1) deficient motheaten (me/me) mice compared with normal littermate controls. Deficiency in myelin and MBP expression in both brains and spinal cords of motheaten mice correlated with reduced MBP mRNA expression levels in vivo and in purified oligodendrocytes in vitro. Therefore, SHP-1 activity seems to be a critical regulator of oligodendrocyte gene expression and function. Consistent with this role, this study demonstrates that oligodendrocytes of motheaten mice and SHP-1-depleted N20.1 cells produce higher levels of reactive oxygen species (ROS) and exhibit corresponding markers of increased oxidative stress. In agreement with these findings, we demonstrate that increased production of ROS coincides with ROS-induced signaling pathways known to affect myelin gene expression in oligodendrocytes. Antioxidant treatment of SHP-1-deficient oligodendrocytes reversed the pathological changes in these cells, with increased myelin protein gene expression and decreased expression of nuclear factor (erythroid-2)-related factor 2 (Nrf2) responsive gene, heme oxygenase-1 (HO-1). Furthermore, we demonstrate that SHP-1 is expressed in human white matter oligodendrocytes, and there is a subset of multiple sclerosis subjects that demonstrate a deficiency of SHP-1 in normal-appearing white matter. These studies reveal critical pathways controlled by SHP-1 in oligodendrocytes that relate to susceptibility of SHP-1-deficient mice to both developmental defects in myelination and to inflammatory demyelinating diseases.

摘要

我们之前曾描述过,与正常同窝对照小鼠相比,含Src同源2结构域的蛋白酪氨酸磷酸酶1(SHP-1)缺陷的动性脑病(me/me)小鼠中枢神经系统中髓鞘形成减少以及相应的髓鞘碱性蛋白(MBP)表达降低。动性脑病小鼠脑和脊髓中髓鞘及MBP表达的缺陷与体内和体外纯化少突胶质细胞中MBP mRNA表达水平降低相关。因此,SHP-1活性似乎是少突胶质细胞基因表达和功能的关键调节因子。与此作用一致,本研究表明动性脑病小鼠的少突胶质细胞和SHP-1缺失的N20.1细胞产生更高水平的活性氧(ROS),并表现出氧化应激增加的相应标志物。与这些发现一致,我们证明ROS产生增加与已知影响少突胶质细胞髓鞘基因表达的ROS诱导信号通路同时出现。对SHP-1缺陷的少突胶质细胞进行抗氧化治疗可逆转这些细胞的病理变化,髓鞘蛋白基因表达增加,核因子(红系-2)相关因子2(Nrf2)反应性基因血红素加氧酶-1(HO-1)的表达降低。此外,我们证明SHP-1在人白质少突胶质细胞中表达,并且有一部分多发性硬化症患者在外观正常的白质中表现出SHP-1缺陷。这些研究揭示了SHP-1在少突胶质细胞中控制的关键途径,这些途径与SHP-1缺陷小鼠对髓鞘形成发育缺陷和炎性脱髓鞘疾病的易感性有关。

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