Li Wei-Peng, Ma Ke, Jiang Xiao-Yan, Yang Rui, Lu Pei-Hua, Nie Bao-Ming, Lu Yang
Department of Nuclear Medicine, the First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui Province, China.
Department of Pharmacy, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Neural Regen Res. 2018 Nov;13(11):1927-1936. doi: 10.4103/1673-5374.239439.
Nerve growth factor (NGF) promotes axonal growth in PC12 cells primarily by regulating the RTK-RAS-MEK-ERK pathway. Panaxydol, a polyacetylene isolated from Panax notoginseng, can mimic the effects of NGF. Panaxydol promotes neurite outgrowth in PC12 cells, but its molecular mechanism remains unclear. Indeed, although alkynol compounds such as panaxydol can increase intracellular cyclic adenosine 3',5'-monophosphate (cAMP) levels and the ERK inhibitor U0126 inhibits alkynol-induced axonal growth, how pathways downstream of cAMP activate ERK have not been investigated. This study observed the molecular mechanism of panaxydol-, NGF- and forskolin-induced PC12 cell axon growth using specific signaling pathway inhibitors. The results demonstrated that although the RTK inhibitor SU5416 obviously inhibited the growth-promoting effect of NGF, it could not inhibit the promoting effect of panaxydol on axonal growth of PC12 cells. The adenylate cyclase inhibitor SQ22536 and cAMP-dependent protein kinase inhibitor RpcAMPS could suppress the promoting effect of forskolin and panaxydol on axonal growth. The ERK inhibitor U0126 inhibited axonal growth induced by all three factors. However, the PKA inhibitor H89 inhibited the promoting effect of forskolin on axonal growth but could not suppress the promoting effect of panaxydol. A western blot assay was used to determine the effects of stimulating factors and inhibitors on ERK phosphorylation levels. The results revealed that NGF activates the ERK pathway through tyrosine receptors to induce axonal growth of PC12 cells. In contrast, panaxydol and forskolin increased cellular cAMP levels and were inhibited by adenylyl cyclase inhibitors. The protein kinase A inhibitor H89 completely inhibited forskolin-induced axonal outgrowth and ERK phosphorylation, but could not inhibit panaxydol-induced axonal growth and ERK phosphorylation. These results indicated that panaxydol promoted axonal growth of PC12 cells through different pathways downstream of cAMP. Considering that exchange protein directly activated by cAMP 1 (Epac1) plays an important role in mediating cAMP signaling pathways, RNA interference experiments targeting the Epac1 gene were employed. The results verified that Epac1 could mediate the axonal growth signaling pathway induced by panaxydol. These findings suggest that compared with NGF and forskolin, panaxydol elicits axonal growth through the cAMP-Epac1-Rap1-MEK-ERK-CREB pathway, which is independent of PKA.
神经生长因子(NGF)主要通过调节RTK-RAS-MEK-ERK信号通路来促进PC12细胞的轴突生长。人参炔醇是从三七中分离得到的一种聚乙炔类化合物,它能够模拟NGF的作用。人参炔醇可促进PC12细胞的神经突生长,但其分子机制尚不清楚。实际上,尽管像人参炔醇这样的炔醇类化合物能够提高细胞内3',5'-环磷酸腺苷(cAMP)水平,且ERK抑制剂U0126可抑制炔醇诱导的轴突生长,但cAMP下游的信号通路如何激活ERK尚未得到研究。本研究使用特定的信号通路抑制剂观察了人参炔醇、NGF和福斯高林诱导PC12细胞轴突生长的分子机制。结果表明,尽管RTK抑制剂SU5416明显抑制了NGF的促生长作用,但它不能抑制人参炔醇对PC12细胞轴突生长的促进作用。腺苷酸环化酶抑制剂SQ22536和cAMP依赖性蛋白激酶抑制剂RpcAMPS可抑制福斯高林和人参炔醇对轴突生长的促进作用。ERK抑制剂U0126抑制了这三种因子诱导的轴突生长。然而,PKA抑制剂H89抑制了福斯高林对轴突生长的促进作用,但不能抑制人参炔醇的促进作用。采用蛋白质免疫印迹法检测刺激因子和抑制剂对ERK磷酸化水平的影响。结果显示,NGF通过酪氨酸受体激活ERK信号通路,从而诱导PC12细胞的轴突生长。相反,人参炔醇和福斯高林提高了细胞内cAMP水平,并被腺苷酸环化酶抑制剂所抑制。蛋白激酶A抑制剂H89完全抑制了福斯高林诱导的轴突生长和ERK磷酸化,但不能抑制人参炔醇诱导的轴突生长和ERK磷酸化。这些结果表明,人参炔醇通过cAMP下游的不同信号通路促进PC12细胞的轴突生长。鉴于直接由cAMP激活的交换蛋白1(Epac1)在介导cAMP信号通路中起重要作用,本研究进行了针对Epac1基因的RNA干扰实验。结果证实,Epac1可介导人参炔醇诱导的轴突生长信号通路。这些发现表明,与人参生长因子和福斯高林相比,人参炔醇通过cAMP-Epac1-Rap1-MEK-ERK-CREB信号通路诱导轴突生长,该通路独立于PKA。