Department of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322
Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA 30322.
eNeuro. 2021 Jan 15;8(1). doi: 10.1523/ENEURO.0155-20.2020. Print 2021 Jan-Feb.
Asparagine endopeptidase (AEP) is a lysosomal protease implicated in the pathology of Alzheimer's disease (AD). It is known to cleave the axonal microtubule associated protein, Tau, and amyloid precursor protein (APP), both of which might impede axon regeneration following peripheral nerve injury (PNI). Active AEP, AEP-cleaved fragments of Tau (Tau N368), and APP (APP N585) were found in injured peripheral nerves. In AEP null mice, elongation of regenerating axons after sciatic nerve transection and repair was increased relative to wild-type (WT) controls. Compound muscle action potentials (M responses) were restored in reinnervated muscles twice as fast after injury in AEP knock-out (KO) mice as WT controls. Neurite elongation in cultures of adult dorsal root ganglion (DRG) neurons derived from AEP KO mice was increased significantly relative to cultures from WT controls. In AEP KO mice exposed to 1 h of 20-Hz electrical stimulation (ES) at the time of nerve injury, no further enhancement of axon regeneration was observed. These findings support inhibition of AEP as a therapeutic target to enhance axon regeneration after PNI.
天冬酰胺内肽酶(AEP)是一种溶酶体蛋白酶,与阿尔茨海默病(AD)的病理学有关。已知它可以切割轴突微管相关蛋白 Tau 和淀粉样前体蛋白(APP),这两者都可能阻碍周围神经损伤(PNI)后的轴突再生。在受伤的周围神经中发现了活性 AEP、AEP 切割的 Tau 片段(Tau N368)和 APP(APP N585)。在 AEP 缺失小鼠中,与野生型(WT)对照相比,坐骨神经横断和修复后再生轴突的伸长增加。与 WT 对照相比,AEP 敲除(KO)小鼠的复合肌肉动作电位(M 反应)在损伤后恢复的速度快了两倍。源自 AEP KO 小鼠的成年背根神经节(DRG)神经元培养物中的神经突伸长显著增加,与源自 WT 对照的培养物相比。在神经损伤时接受 1 小时 20-Hz 电刺激(ES)的 AEP KO 小鼠中,未观察到轴突再生的进一步增强。这些发现支持抑制 AEP 作为治疗靶点,以增强 PNI 后的轴突再生。