Department of Neurological, Neuropsychological, Morphological and Motor Sciences, Section of Physiology, University of Verona, Verona, Italy.
PLoS One. 2013 May 29;8(5):e64350. doi: 10.1371/journal.pone.0064350. Print 2013.
In adult mammals, after optic nerve injury, retinal ganglion cells (RGCs) do not regenerate their axons and most of them die by apoptosis within a few days. Recently, several strategies that activate neuronal intracellular pathways were proposed to prevent such degenerative processes. The rho-related small GTPase Rac1 is part of a complex, still not fully understood, intracellular signaling network, mediating in neurons many effects, including axon growth and cell survival. However, its role in neuronal survival and regeneration in vivo has not yet been properly investigated. To address this point we intravitreally injected selective cell-penetrating Rac1 mutants after optic nerve crush and studied the effect on RGC survival and axonal regeneration. We injected two well-characterized L61 constitutively active Tat-Rac1 fusion protein mutants, in which a second F37A or Y40C mutation confers selectivity in downstream signaling pathways. Results showed that, 15 days after crush, both mutants were able to improve survival and to prevent dendrite degeneration, while the one harboring the F37A mutation also improved axonal regeneration. The treatment with F37A mutant for one month did not improve the axonal elongation respect to 15 days. Furthermore, we found an increase of Pak1 T212 phosphorylation and ERK1/2 expression in RGCs after F37A treatment, whereas ERK1/2 was more activated in glial cells after Y40C administration. Our data suggest that the selective activation of distinct Rac1-dependent pathways could represent a therapeutic strategy to counteract neuronal degenerative processes in the retina.
在成年哺乳动物中,视神经损伤后,视网膜神经节细胞(RGC)不会再生其轴突,并且大多数在几天内通过细胞凋亡而死亡。最近,提出了几种激活神经元细胞内途径的策略来防止这种退行性过程。Rho 相关的小 GTP 酶 Rac1 是一个复杂的,尚未完全理解的细胞内信号网络的一部分,在神经元中介导许多效应,包括轴突生长和细胞存活。然而,其在体内神经元存活和再生中的作用尚未得到适当研究。为了解决这一问题,我们在视神经挤压后通过玻璃体内注射选择性穿透细胞的 Rac1 突变体,并研究了其对 RGC 存活和轴突再生的影响。我们注射了两种经过充分表征的 L61 组成型激活 Tat-Rac1 融合蛋白突变体,其中第二个 F37A 或 Y40C 突变赋予下游信号通路的选择性。结果表明,在挤压后 15 天,两种突变体均能够改善存活并防止树突退化,而携带 F37A 突变的突变体还能够改善轴突再生。用 F37A 突变体治疗一个月不会改善轴突伸长相对于 15 天的情况。此外,我们发现 F37A 处理后 RGC 中 Pak1 T212 磷酸化和 ERK1/2 表达增加,而 Y40C 给药后 ERK1/2 在神经胶质细胞中更活跃。我们的数据表明,选择性激活不同的 Rac1 依赖性途径可能代表一种治疗策略,以对抗视网膜中的神经元退行性过程。