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mTORC1 参与 DGKβ 诱导的轴突生长和棘突生成。

mTORC1 is involved in DGKβ-induced neurite outgrowth and spinogenesis.

机构信息

Department of Applied Chemistry in Bioscience, Graduate School of Agricultural Sciences & Faculty of Agriculture, Kobe University, Kobe, Japan.

Laboratory of Cell Signaling, Biosignal Research Center, Kobe University, Kobe, Japan.

出版信息

Neurochem Int. 2020 Mar;134:104645. doi: 10.1016/j.neuint.2019.104645. Epub 2019 Dec 28.

Abstract

Diacylglycerol kinase β (DGKβ) is an enzyme converting DG to phosphatidic acid (PA) and is specifically expressed in neurons, especially those in the cerebral cortex, hippocampus and striatum. We previously reported that DGKβ induces neurite outgrowth and spinogenesis, contributing to higher brain function including emotion and memory, and plasma membrane localization of DGKβ via the C1 domain and a cluster of basic amino acids at the C-terminus is necessary for its function. To clarify the mechanisms involved in neuronal development by DGKβ, we investigated whether DGKβ activity induces neurite outgrowth using human neuroblastoma SH-SY5Y cells. DGKβ induced neurite outgrowth by activation of mammalian target of rapamycin complex 1 (mTORC1) through a kinase-dependent pathway. In addition, in primary cultured cortical and hippocampal neurons, inhibition of mTORC1 abolished DGKβ induced-neurite outgrowth, branching and spinogenesis. These results indicated that DGKβ induces neurite outgrowth and spinogenesis by activating mTORC1 in a kinase-dependent pathway.

摘要

二酰基甘油激酶β(DGKβ)是一种将 DG 转化为磷脂酸(PA)的酶,特异性表达于神经元,特别是大脑皮层、海马和纹状体中的神经元。我们之前的研究报道,DGKβ 诱导轴突生长和棘突形成,促进包括情感和记忆在内的高级脑功能,DGKβ 通过 C1 结构域和 C 末端的碱性氨基酸簇定位于质膜,这对于其功能是必需的。为了阐明 DGKβ 参与神经元发育的机制,我们使用人神经母细胞瘤 SH-SY5Y 细胞研究了 DGKβ 活性是否诱导轴突生长。DGKβ 通过激酶依赖性途径激活哺乳动物雷帕霉素靶蛋白复合物 1(mTORC1)诱导轴突生长。此外,在原代培养的皮质和海马神经元中,抑制 mTORC1 消除了 DGKβ 诱导的轴突生长、分支和棘突形成。这些结果表明,DGKβ 通过激酶依赖性途径激活 mTORC1 诱导轴突生长和棘突形成。

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