Laboratory of Neurophysiology and Plasticity, IRCCS Fondazione Santa Lucia, 00143 Rome, Italy.
Department of Systems Medicine, University of Rome "Tor Vergata", 00133 Rome, Italy.
Int J Mol Sci. 2019 Jul 11;20(14):3407. doi: 10.3390/ijms20143407.
Caspases are a family of conserved cysteine proteases that play key roles in multiple cellular processes, including programmed cell death and inflammation. Recent evidence shows that caspases are also involved in crucial non-apoptotic functions, such as dendrite development, axon pruning, and synaptic plasticity mechanisms underlying learning and memory processes. The activated form of caspase-3, which is known to trigger widespread damage and degeneration, can also modulate synaptic function in the adult brain. Thus, in the present study, we tested the hypothesis that caspase-3 modulates synaptic plasticity at corticostriatal synapses in the phosphatase and tensin homolog (PTEN) induced kinase 1 (PINK1) mouse model of Parkinson's disease (PD). Loss of PINK1 has been previously associated with an impairment of corticostriatal long-term depression (LTD), rescued by amphetamine-induced dopamine release. Here, we show that caspase-3 activity, measured after LTD induction, is significantly decreased in the PINK1 knockout model compared with wild-type mice. Accordingly, pretreatment of striatal slices with the caspase-3 activator α-(Trichloromethyl)-4-pyridineethanol (PETCM) rescues a physiological LTD in PINK1 knockout mice. Furthermore, the inhibition of caspase-3 prevents the amphetamine-induced rescue of LTD in the same model. Our data support a hormesis-based double role of caspase-3; when massively activated, it induces apoptosis, while at lower level of activation, it modulates physiological phenomena, like the expression of corticostriatal LTD. Exploring the non-apoptotic activation of caspase-3 may contribute to clarify the mechanisms involved in synaptic failure in PD, as well as in view of new potential pharmacological targets.
半胱天冬酶是一组保守的半胱氨酸蛋白酶,在包括程序性细胞死亡和炎症在内的多种细胞过程中发挥关键作用。最近的证据表明,半胱天冬酶也参与了至关重要的非凋亡功能,如树突发育、轴突修剪以及学习和记忆过程中涉及的突触可塑性机制。众所周知,激活的 caspase-3 会引发广泛的损伤和退化,也可以调节成年大脑中的突触功能。因此,在本研究中,我们检验了以下假设:在帕金森病(PD)的磷酸酶和张力蛋白同系物(PTEN)诱导的激酶 1(PINK1)小鼠模型中,caspase-3 调节皮质纹状体突触的突触可塑性。先前的研究表明,PINK1 的缺失与皮质纹状体长时程抑制(LTD)的损害有关,这种损害可被安非他命诱导的多巴胺释放所挽救。在这里,我们发现与野生型小鼠相比,LTD 诱导后 caspase-3 活性在 PINK1 敲除模型中显著降低。因此,用 caspase-3 激活剂α-(三氯甲基)-4-吡啶乙醇(PETCM)预处理纹状体切片可挽救 PINK1 敲除小鼠的生理 LTD。此外,抑制 caspase-3 可防止在相同模型中安非他命诱导 LTD 的恢复。我们的数据支持 caspase-3 的基于激素的双重作用假说;当大量激活时,它会诱导细胞凋亡,而在较低水平的激活时,它会调节生理现象,如皮质纹状体 LTD 的表达。探索 caspase-3 的非凋亡激活可能有助于阐明 PD 中突触衰竭涉及的机制,并考虑到新的潜在药理学靶点。