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凋亡诱导因子和亲环素 A 在肌萎缩侧索硬化症模型小鼠中转位到运动神经元核。

Apoptosis-inducing factor and cyclophilin A cotranslocate to the motor neuronal nuclei in amyotrophic lateral sclerosis model mice.

机构信息

Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University, Daigaku-nishi, Gifu, Japan.

出版信息

CNS Neurosci Ther. 2011 Oct;17(5):294-304. doi: 10.1111/j.1755-5949.2010.00180.x. Epub 2010 Jun 14.

Abstract

AIMS

Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease whose mechanism is not understood. Recently, it was reported that apoptosis-inducing factor (AIF) was involved in motor neuronal cell death in ALS model mice, and AIF-induced neuronal cell death by interacting with cyclophilin A (CypA). However, it is unknown whether the CypA and AIF-complex induces chromatinolysis in ALS. Therefore, in the present study, we investigated the process of motor neuron degeneration as the disease progresses and to determine whether the CypA-AIF complex would play a role in inducing motor neuronal cell death in mutant superoxide dismutase 1 (SOD1)(G93A) ALS model mice.

METHODOLOGY

We prepared the nuclear fractions of spinal cords and demonstrated the nuclear translocation of CypA with AIF in SOD1(G93A) mice by immunoprecipitation. The localization of CypA and AIF in the spinal cords was assessed by immunohistochemistry.

RESULTS

In the spinal cords of SOD1(G93A) mice, the expressions of CypA and AIF were detected in the motor neurons, and CypA and AIF cotranslocated to the motor neuronal nuclei with CypA. Furthermore, the expression of CypA was detected in GFAP-positive astrocytes, but not in CD11b-positive microglial cells. On the other hand, these findings were not detected in the spinal cords of wild-type mice.

CONCLUSIONS

From these results, we suggest that CypA and AIF may play cooperative and pivotal roles in motor neuronal death in the murine ALS model.

摘要

目的

肌萎缩侧索硬化症(ALS)是一种致命的运动神经元疾病,其发病机制尚不清楚。最近有报道称,凋亡诱导因子(AIF)参与了 ALS 模型小鼠运动神经元细胞死亡,并且 AIF 通过与亲环素 A(CypA)相互作用诱导神经元细胞死亡。然而,尚不清楚 CypA 和 AIF 复合物是否会在 ALS 中诱导染色质溶解。因此,在本研究中,我们研究了运动神经元退化的过程,以确定 CypA-AIF 复合物是否会在突变型超氧化物歧化酶 1(SOD1)(G93A)ALS 模型小鼠中诱导运动神经元死亡。

方法

我们制备了脊髓核部分,并通过免疫沉淀证明了 CypA 与 AIF 在 SOD1(G93A)小鼠中的核转位。通过免疫组织化学评估 CypA 和 AIF 在脊髓中的定位。

结果

在 SOD1(G93A)小鼠的脊髓中,在运动神经元中检测到 CypA 和 AIF 的表达,并且 CypA 和 AIF 与 CypA 共转位到运动神经元核中。此外,在 GFAP 阳性星形胶质细胞中检测到 CypA 的表达,但在 CD11b 阳性小胶质细胞中未检测到。另一方面,在野生型小鼠的脊髓中未发现这些发现。

结论

从这些结果来看,我们认为 CypA 和 AIF 可能在小鼠 ALS 模型中的运动神经元死亡中发挥协同和关键作用。

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