Luo Jian-Min, Cen Ling-Ping, Zhang Xin-Mei, Chiang Sylvia Wai-Yee, Huang Yao, Lin Dusheng, Fan You-Ming, van Rooijen Nico, Lam Dennis Shun Chiu, Pang Chi Pui, Cui Qi
Joint Shantou International Eye Center of Shantou University, Shantou, China.
Eur J Neurosci. 2007 Aug;26(4):828-42. doi: 10.1111/j.1460-9568.2007.05718.x.
Recently we unexpectedly found that PI3K/akt, JAK/STAT and MEK/ERK pathway inhibitors enhanced retinal ganglion cell (RGC) survival after optic nerve (ON) axotomy in adult rat, a phenomenon contradictory to conventional belief that these pathways are pro-survival. In this study we showed that: (i) the RGC protection was pathway inhibition-dependent; (ii) inhibition of PI3K/akt and JAK/STAT, but not MEK/ERK, activated macrophages in the eye, (iii) macrophage removal from the eye using clodronate liposomes significantly impeded PI3K/akt and JAK/STAT inhibition-induced RGC survival and axon regeneration whereas it only slightly affected MEK/ERK inhibition-dependent protection; (iv) in the absence of recruited macrophages in the eye, inhibition of PI3K/akt or JAK/STAT did not influence RGC survival; and (v) strong PI3K/akt, JAK/STAT and MEK/ERK pathway activities were located in RGCs but not macrophages after ON injury. In retinal explants, in which supply of blood-derived macrophages is absent, MEK/ERK inhibition promoted RGC survival whereas PI3K/akt or JAK/STAT inhibition had no effect on RGC viability. However, MEK/ERK inhibition exerted opposite effects on the viability of purified adult RGCs at different concentrations in vitro, suggesting that this pathway may be bifunctional depending on the level of pathway activity. Our data thus demonstrate that inhibition of the PI3K/akt or JAK/STAT pathway activated macrophages to facilitate RGC protection after ON injury whereas the two pathways per se did not modulate RGC viability under the injury conditions (in the absence of the pathway activators). In contrast, the MEK/ERK pathway inhibition protected RGCs via macrophage-independent mechanism(s).
最近,我们意外地发现,PI3K/akt、JAK/STAT和MEK/ERK信号通路抑制剂可增强成年大鼠视神经切断术后视网膜神经节细胞(RGC)的存活,这一现象与传统观念相悖,传统观念认为这些信号通路具有促存活作用。在本研究中,我们发现:(i)RGC的保护作用依赖于信号通路抑制;(ii)抑制PI3K/akt和JAK/STAT信号通路,而非MEK/ERK信号通路,可激活眼中的巨噬细胞;(iii)使用氯膦酸脂质体清除眼中的巨噬细胞,可显著阻碍PI3K/akt和JAK/STAT抑制诱导的RGC存活和轴突再生,而对MEK/ERK抑制依赖性保护作用仅有轻微影响;(iv)在眼中没有募集到巨噬细胞的情况下,抑制PI3K/akt或JAK/STAT信号通路不会影响RGC的存活;(v)视神经损伤后,强烈的PI3K/akt、JAK/STAT和MEK/ERK信号通路活性位于RGC中,而非巨噬细胞中。在没有血液来源巨噬细胞供应的视网膜外植体中,抑制MEK/ERK信号通路可促进RGC存活,而抑制PI3K/akt或JAK/STAT信号通路对RGC活力没有影响。然而,MEK/ERK信号通路抑制在体外不同浓度下对纯化的成年RGC活力产生相反的影响,这表明该信号通路可能具有双功能,具体取决于信号通路活性水平。因此,我们的数据表明,抑制PI3K/akt或JAK/STAT信号通路可激活巨噬细胞,从而促进视神经损伤后RGC的保护,而在损伤条件下(在没有信号通路激活剂的情况下),这两条信号通路本身并不会调节RGC的活力。相比之下,抑制MEK/ERK信号通路通过不依赖巨噬细胞的机制保护RGC。