Sainath Rajiv, Gallo Gianluca
Shriners Hospitals Pediatric Research Center, Lewis Katz School of Medicine, Temple University, Philadelphia, PA, United States.
Department of Neural Sciences, Lewis Katz School of Medicine, Temple University, Philadelphia, PA, United States.
Front Mol Neurosci. 2021 Sep 24;14:726331. doi: 10.3389/fnmol.2021.726331. eCollection 2021.
Nerve Growth Factor (NGF) promotes the elaboration of axonal filopodia and branches through PI3K-Akt. NGF activates the TrkA receptor resulting in an initial transient high amplitude burst of PI3K-Akt signaling followed by a maintained lower steady state, hereafter referred to as initiation and steady state phases. Akt initially undergoes phosphorylation at T308 followed by phosphorylation at S473, resulting in maximal kinase activation. We report that during the initiation phase the localization of PI3K signaling, reported by visualizing sites of PIP3 formation, and Akt signaling, reflected by Akt phosphorylation at T308, correlates with the positioning of axonal mitochondria. Mitochondrial oxidative phosphorylation but not glycolysis is required for Akt phosphorylation at T308. In contrast, the phosphorylation of Akt at S473 is not spatially associated with mitochondria and is dependent on both oxidative phosphorylation and glycolysis. Under NGF steady state conditions, maintenance of phosphorylation at T308 shows dual dependence on oxidative phosphorylation and glycolysis. Phosphorylation at S473 is more dependent on glycolysis but also requires oxidative phosphorylation for maintenance over longer time periods. The data indicate that NGF induced PI3K-Akt signaling along axons is preferentially initiated at sites containing mitochondria, in a manner dependent on oxidative phosphorylation. Steady state signaling is discussed in the context of combined contributions by mitochondria and the possibility of glycolysis occurring in association with endocytosed signalosomes.
神经生长因子(NGF)通过PI3K-Akt促进轴突丝状伪足和分支的形成。NGF激活TrkA受体,导致PI3K-Akt信号传导最初出现短暂的高幅度爆发,随后维持在较低的稳态,以下分别称为起始阶段和稳态阶段。Akt最初在T308位点发生磷酸化,随后在S473位点磷酸化,从而实现最大程度的激酶激活。我们报告,在起始阶段,通过可视化PIP3形成位点报告的PI3K信号定位以及通过Akt在T308位点的磷酸化反映的Akt信号定位,与轴突线粒体的定位相关。T308位点的Akt磷酸化需要线粒体氧化磷酸化而非糖酵解。相反,S473位点的Akt磷酸化与线粒体在空间上无关联,并且依赖于氧化磷酸化和糖酵解两者。在NGF稳态条件下,T308位点磷酸化的维持对氧化磷酸化和糖酵解都有双重依赖性。S473位点的磷酸化更依赖于糖酵解,但在较长时间内维持也需要氧化磷酸化。数据表明,NGF诱导的轴突PI3K-Akt信号传导优先在含有线粒体的位点起始,其方式依赖于氧化磷酸化。在结合线粒体的贡献以及与内吞信号小体相关联发生糖酵解的可能性的背景下讨论了稳态信号传导。