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Caspase-3 在帕金森病 PINK1 小鼠模型中非凋亡作用的丧失。

Loss of Non-Apoptotic Role of Caspase-3 in the PINK1 Mouse Model of Parkinson's Disease.

机构信息

Laboratory of Neurophysiology and Plasticity, IRCCS Fondazione Santa Lucia, 00143 Rome, Italy.

Department of Systems Medicine, University of Rome "Tor Vergata", 00133 Rome, Italy.

出版信息

Int J Mol Sci. 2019 Jul 11;20(14):3407. doi: 10.3390/ijms20143407.

Abstract

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.

摘要

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。

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