Wales Samantha Q, Li Baiquan, Laing Jennifer M, Aurelian Laure
Department of Pharmacology and Experimental Therapeutics, University of Maryland School of Medicine, Baltimore, Maryland, USA.
J Neurochem. 2007 Oct;103(1):365-79. doi: 10.1111/j.1471-4159.2007.04745.x.
The herpes simplex virus type 2 (HSV-2) protein ICP10PK has anti-apoptotic activity in virus-infected hippocampal cultures through activation of the Ras/Raf-1/MEK/ERK pathway. To exclude the possible contribution of other viral proteins to cell fate determination, we examined the survival of primary hippocampal cultures and neuronally differentiated PC12 cells transfected with ICP10PK from apoptosis caused by nerve growth factor (NGF) withdrawal. NGF deprivation caused apoptosis in cultures mock-transfected or transfected with the kinase-negative ICP10 mutant p139(TM), but not in ICP10PK-transfected cultures. In one clone (PC47), ICP10PK inhibited caspase-3 activation through up-regulation/stabilization of adenylate cyclase (AC), activation of PKA and MEK, and the convergence of the two pathways on extracellular signal-regulated kinase activation. The anti-apoptotic proteins Bag-1 and Bcl-2 were stabilized and the pro-apoptotic protein Bad was phosphorylated (inactivated). In another clone (PC70), ICP10PK inhibited apoptosis through MEK-dependent up-regulation of the anti-apoptotic protein XIAP (that inhibits the activity of processed caspase-3) and down-regulation of the apoptogenic protein Smac/DIABLO. This may be cell-type specific, but the baculovirus p35 protein did not potentiate the neuroprotective activity of ICP10PK in PC12 cells, suggesting that ICP10PK inhibits both caspase activation and activity. The data indicate that ICP10PK inhibits apoptosis independent of other viral proteins and is a promising neuronal gene therapy platform.
2型单纯疱疹病毒(HSV-2)蛋白ICP10PK通过激活Ras/Raf-1/MEK/ERK途径,在病毒感染的海马培养物中具有抗凋亡活性。为了排除其他病毒蛋白对细胞命运决定的可能影响,我们检测了原代海马培养物和经神经生长因子(NGF)撤除诱导凋亡后转染ICP10PK的神经分化PC12细胞的存活情况。NGF剥夺导致mock转染或转染激酶阴性ICP10突变体p139(TM)的培养物发生凋亡,但在转染ICP10PK的培养物中未出现凋亡。在一个克隆(PC47)中,ICP10PK通过上调/稳定腺苷酸环化酶(AC)、激活PKA和MEK以及两条途径在细胞外信号调节激酶激活上的汇聚,抑制了caspase-3的激活。抗凋亡蛋白Bag-1和Bcl-2得到稳定,促凋亡蛋白Bad被磷酸化(失活)。在另一个克隆(PC70)中,ICP10PK通过MEK依赖的抗凋亡蛋白XIAP(抑制加工后的caspase-3活性)上调和凋亡诱导蛋白Smac/DIABLO下调来抑制凋亡。这可能具有细胞类型特异性,但杆状病毒p35蛋白并未增强ICP10PK在PC12细胞中的神经保护活性,表明ICP10PK抑制caspase的激活和活性。数据表明,ICP10PK独立于其他病毒蛋白抑制凋亡,是一个有前景的神经元基因治疗平台。