首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Interaction of Synaptosomal-Associated Protein 25 with Neutral Sphingomyelinase 2: Functional Impact on the Sphingomyelin Pathway
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Interaction of Synaptosomal-Associated Protein 25 with Neutral Sphingomyelinase 2: Functional Impact on the Sphingomyelin Pathway

机译:突触体相关蛋白25与中性鞘氨酰胺酶2的相互作用:对鞘磷脂途径的功能影响

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摘要

Neurotransmitter release is mediated by ceramide, which is generated by sphingomyelin hydrolysis. In the present study, we examined whether synaptosomal-associated protein 25 (SNAP-25) is involved in ceramide production and exocytosis. Neutral sphingomyelinase 2 (nSMase2) was partially purified from bovine brain and we found that SNAP-25 was enriched in the nSMase2-containing fractions. In rat synaptosomes and PC12 cells, the immunoprecipitation pellet of anti-SNAP-25 antibody showed higher nSMase activity than the immunoprecipitation pellet of anti-nSMase2 antibody. In PC12 cells, SNAP-25 was colocalized with nSMase2. Transfection of SNAP-25 small interfering RNA (siRNA) significantly inhibited nSMase2 translocation to the plasma membrane. A23187-induced ceramide production was concomitantly reduced in SNAP-25 siRNA-transfected PC12 cells compared with that in scrambled siRNA-transfected cells. Moreover, transfection of SNAP-25 siRNA inhibited dopamine release, whereas addition of C-6-ceramide to the siRNA-treated cells moderately reversed this inhibition. Additionally, nSMase2 inhibition reduced dopamine release. Collectively, our results indicate that SNAP-25 interacts with nSMase2 during ceramide production, which mediates exocytosis and neurotransmitter release. (C) 2019 Published by Elsevier Ltd on behalf of IBRO.
机译:神经递质释放由神经酰胺介导,由鞘氨酰胺水解产生。在本研究中,我们检查了突触体相关蛋白25(SNAP-25)是否参与神经酰胺生产和外尿作用。中性鞘氨基氨基酶2(NSMase2)部分纯化牛脑,并且我们发现富含含有Nmase2的级分的牛排25。在大鼠突触体和PC12细胞中,抗​​锥-25抗体的免疫沉淀颗粒显示出比抗NMase2抗体的免疫沉淀颗粒更高的NSmase活性。在PC12细胞中,SNAP-25用NSMase2分开。 SNAP-25小干扰RNA(siRNA)的转染显着抑制了血浆膜的NSMASE2易位。与糖化的siRNA转染的细胞相比,A23187诱导的神经酰胺产生在牛血酮转染的PC12细胞中伴随着减少。此外,转染卡扣-25 siRNA抑制多巴胺释放,而向SiRNA处理的细胞中加入C-6-神经酰胺,适度反转该抑制。另外,NSMase2抑制减少了多巴胺释放。统称,我们的结果表明,SNAP-25在神经酰胺生产过程中与NSMase2相互作用,该氨胺产生介导外毒性和神经递质释放。 (c)2019年由elsevier有限公司代表银布发布。

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