Mayo Graduate School, College of Medicine, Mayo Clinic, Rochester, Minnesota 55905, USA.
J Neurosci. 2011 May 11;31(19):7016-27. doi: 10.1523/JNEUROSCI.0216-11.2011.
The action of many extracellular guidance cues on axon pathfinding requires Ca2+ influx at the growth cone (Hong et al., 2000; Nishiyama et al., 2003; Henley and Poo, 2004), but how activation of guidance cue receptors leads to opening of plasmalemmal ion channels remains largely unknown. Analogous to the chemotaxis of amoeboid cells (Parent et al., 1998; Servant et al., 2000), we found that a gradient of chemoattractant triggered rapid asymmetric PI(3,4,5)P3 accumulation at the growth cone's leading edge, as detected by the translocation of a GFP-tagged binding domain of Akt in Xenopus laevis spinal neurons. Growth cone chemoattraction required PI(3,4,5)P3 production and Akt activation, and genetic perturbation of polarized Akt activity disrupted axon pathfinding in vitro and in vivo. Furthermore, patch-clamp recording from growth cones revealed that exogenous PI(3,4,5)P3 rapidly activated TRP (transient receptor potential) channels, and asymmetrically applied PI(3,4,5)P3 was sufficient to induce chemoattractive growth cone turning in a manner that required downstream Ca2+ signaling. Thus, asymmetric PI(3,4,5)P3 elevation and Akt activation are early events in growth cone chemotaxis that link receptor activation to TRP channel opening and Ca2+ signaling. Altogether, our findings reveal that PI(3,4,5)P3 elevation polarizes to the growth cone's leading edge and can serve as an early regulator during chemotactic guidance.
许多细胞外导向线索在轴突寻迹中的作用需要生长锥内的 Ca2+ 内流(Hong 等人,2000;Nishiyama 等人,2003;Henley 和 Poo,2004),但导向线索受体的激活如何导致质膜离子通道的打开在很大程度上仍是未知的。类似于变形虫细胞的趋化性(Parent 等人,1998;Servant 等人,2000),我们发现,趋化剂梯度在生长锥的前缘触发了快速的不对称 PI(3,4,5)P3 积累,这可通过 GFP 标记的 Akt 结合域在非洲爪蟾脊髓神经元中的易位来检测。生长锥的趋化性需要 PI(3,4,5)P3 的产生和 Akt 的激活,并且极化 Akt 活性的遗传干扰破坏了体外和体内的轴突寻迹。此外,从生长锥进行的膜片钳记录显示,外源性 PI(3,4,5)P3 可快速激活 TRP(瞬时受体电位)通道,并且不对称施加的 PI(3,4,5)P3 足以以需要下游 Ca2+ 信号的方式诱导趋化性生长锥转向。因此,不对称的 PI(3,4,5)P3 升高和 Akt 激活是生长锥趋化性的早期事件,它将受体激活与 TRP 通道打开和 Ca2+ 信号联系起来。总的来说,我们的发现表明,PI(3,4,5)P3 的升高使生长锥极化到前缘,并可作为趋化性导向过程中的早期调节剂。