Secondo Agnese, Esposito Alba, Petrozziello Tiziana, Boscia Francesca, Molinaro Pasquale, Tedeschi Valentina, Pannaccione Anna, Ciccone Roselia, Guida Natascia, Di Renzo Gianfranco, Annunziato Lucio
1Division of Pharmacology, Department of Neuroscience, Reproductive and Odontostomatological Sciences, School of Medicine, "Federico II" University of Naples, Naples, Italy.
2Fondazione IRCCS SDN, Naples, Italy.
Cell Death Discov. 2018 Feb 7;4:12. doi: 10.1038/s41420-017-0018-1. eCollection 2018 Dec.
Nuclear envelope (NE) is a Ca-storing organelle controlling neuronal differentiation through nuclear Ca concentrations ([Ca]). However, how [Ca] regulates this important function remains unknown. Here, we investigated the role of the nuclear form of the Na/Ca exchanger 1(nuNCX1) during the different stages of neuronal differentiation and the involvement of PTEN/PI3'K/Akt pathway. In neuronal cells, nuNCX1 was detected on the inner membrane of the NE where protein expression and activity of the exchanger increased during NGF-induced differentiation. nuNCX1 activation by Na-free perfusion induced a time-dependent activation of nuclear-resident PI3K/Akt pathway in isolated nuclei. To discriminate the contribution of nuNCX1 from those of plasma membrane NCX, we generated a chimeric protein composed of the fluorophore EYFP, the exchanger inhibitory peptide, and the nuclear localization signal, named XIP-NLS. Fura-2 measurements on single nuclei and patch-clamp experiments in whole-cell configuration showed that XIP-NLS selectively inhibited nuNCX1. Once it reached the nuclear compartment, XIP-NLS increased the nucleoplasmic Ca peak elicited by ATP and reduced Akt phosphorylation, GAP-43 and MAP-2 expression through nuclear-resident PTEN induction. Furthermore, in accordance with the prevention of the neuronal phenotype, XIP-NLS significantly reduced TTX-sensitive Na currents and membrane potential during neuronal differentiation. The selective inhibition of nuNCX1 by XIP-NLS increased the percentage of β III tubulin-positive immature neurons in mature cultures of MAP-2-positive cortical neurons, thus unraveling a new function for nuNCX1 in regulating neuronal differentiation through [Ca]-dependent PTEN/PI3K/Akt pathway.
核膜(NE)是一种储存钙的细胞器,通过核钙浓度([Ca])控制神经元分化。然而,[Ca]如何调节这一重要功能仍不清楚。在这里,我们研究了钠钙交换蛋白1的核形式(nuNCX1)在神经元分化不同阶段的作用以及PTEN/PI3'K/Akt信号通路的参与情况。在神经元细胞中,nuNCX1定位于核膜内膜,在神经生长因子(NGF)诱导的分化过程中,该交换蛋白的表达和活性增加。无钠灌注激活nuNCX1可在分离的细胞核中诱导核内PI3K/Akt信号通路的时间依赖性激活。为了区分nuNCX1与质膜NCX的作用,我们构建了一种由荧光蛋白EYFP、交换蛋白抑制肽和核定位信号组成的嵌合蛋白,命名为XIP-NLS。对单个细胞核进行Fura-2测量以及在全细胞模式下进行膜片钳实验表明,XIP-NLS可选择性抑制nuNCX1。一旦进入核区室,XIP-NLS会增加ATP引起的核质钙峰,并通过诱导核内PTEN减少Akt磷酸化、生长相关蛋白43(GAP-43)和微管相关蛋白2(MAP-2)的表达。此外,与神经元表型的抑制一致,XIP-NLS在神经元分化过程中显著降低了河豚毒素敏感的钠电流和膜电位。XIP-NLS对nuNCX1的选择性抑制增加了成熟培养的MAP-2阳性皮质神经元中β III微管蛋白阳性未成熟神经元的比例,从而揭示了nuNCX1通过依赖钙的PTEN/PI3K/Akt信号通路调节神经元分化的新功能。