Bouquier Nathalie, Girard Benoit, Aparicio Arias Juri, Fagni Laurent, Bertaso Federica, Perroy Julie
IGF, Université de Montpellier, CNRS, INSERM, Montpellier, France.
Front Synaptic Neurosci. 2020 Apr 21;12:15. doi: 10.3389/fnsyn.2020.00015. eCollection 2020.
Epileptogenesis is the gradual process responsible for converting a healthy brain into an epileptic brain. This process can be triggered by a wide range of factors, including brain injury or tumors, infections, and status epilepticus. Epileptogenesis results in aberrant synaptic plasticity, neuroinflammation and seizure-induced cell death. As Matrix Metalloproteinases (MMPs) play a crucial role in cellular plasticity by remodeling the extracellular matrix (ECM), gelatinases (MMP-2 and MMP-9) were recently highlighted as key players in epileptogenesis. In this work, we engineered a biosensor to report gelatinase activity in a model of epileptogenesis. This biosensor encompasses a gelatinase-sensitive activatable cell penetrating peptide (ACPP) coupled to a TAMRA fluorophore, allowing fluorescence uptake in cells displaying endogenous gelatinase activities. In a preclinical mouse model of temporal lobe epilepsy (TLE), the intrahippocampal kainate injection, ACPPs revealed a localized distribution of gelatinase activities, refining temporal cellular changes during epileptogenesis. The activity was found particularly but not only in the ipsilateral hippocampus, starting from the CA1 area and spreading to dentate gyrus from the early stages throughout chronic epilepsy, notably in neurons and microglial cells. Thus, our work shows that ACPPs are suitable molecular imaging probes for detecting the spatiotemporal pattern of gelatinase activity during epileptogenesis, suggesting their possible use as vectors to target cellular reactive changes with treatment for epileptogenesis.
癫痫发生是一个渐进的过程,它会使健康大脑转变为癫痫大脑。这个过程可能由多种因素触发,包括脑损伤或肿瘤、感染以及癫痫持续状态。癫痫发生会导致异常的突触可塑性、神经炎症和癫痫发作诱导的细胞死亡。由于基质金属蛋白酶(MMPs)通过重塑细胞外基质(ECM)在细胞可塑性中发挥关键作用,明胶酶(MMP - 2和MMP - 9)最近被认为是癫痫发生的关键因素。在这项研究中,我们设计了一种生物传感器来报告癫痫发生模型中的明胶酶活性。这种生物传感器包含一个与TAMRA荧光团偶联的对明胶酶敏感的可激活细胞穿透肽(ACPP),使得在显示内源性明胶酶活性的细胞中能够摄取荧光。在颞叶癫痫(TLE)的临床前小鼠模型中,通过海马内注射红藻氨酸,ACPPs揭示了明胶酶活性的局部分布,细化了癫痫发生过程中的时间性细胞变化。这种活性尤其在同侧海马中被发现,但不仅限于此,从早期到慢性癫痫阶段,从CA1区域开始并扩散到齿状回,特别是在神经元和小胶质细胞中。因此,我们的研究表明,ACPPs是检测癫痫发生过程中明胶酶活性时空模式的合适分子成像探针,这表明它们可能用作靶向细胞反应性变化以治疗癫痫发生的载体。