Instituto de Farmacologia e Neurociências, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisbon, Portugal; Instituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisbon, Portugal.
Instituto de Farmacologia e Neurociências, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisbon, Portugal; Instituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisbon, Portugal; Research Institute for Medicines (iMed.ULisboa), Faculdade de Farmácia, Universidade de Lisboa, 1649-003 Lisbon, Portugal.
Mol Ther. 2024 Oct 2;32(10):3372-3401. doi: 10.1016/j.ymthe.2024.08.022. Epub 2024 Aug 27.
In Alzheimer's disease (AD), amyloid β (Aβ)-triggered cleavage of TrkB-FL impairs brain-derived neurotrophic factor (BDNF) signaling, thereby compromising neuronal survival, differentiation, and synaptic transmission and plasticity. Using cerebrospinal fluid and postmortem human brain samples, we show that TrkB-FL cleavage occurs from the early stages of the disease and increases as a function of pathology severity. To explore the therapeutic potential of this disease mechanism, we designed small TAT-fused peptides and screened their ability to prevent TrkB-FL receptor cleavage. Among these, a TAT-TrkB peptide with a lysine-lysine linker prevented TrkB-FL cleavage both in vitro and in vivo and rescued synaptic deficits induced by oligomeric Aβ in hippocampal slices. Furthermore, this TAT-TrkB peptide improved the cognitive performance, ameliorated synaptic plasticity deficits and prevented Tau pathology progression in vivo in the 5XFAD mouse model of AD. No evidence of liver or kidney toxicity was found. We provide proof-of-concept evidence for the efficacy and safety of this therapeutic strategy and anticipate that this TAT-TrkB peptide has the potential to be a disease-modifying drug that can prevent and/or reverse cognitive deficits in patients with AD.
在阿尔茨海默病(AD)中,淀粉样蛋白β(Aβ)触发 TrkB-FL 的裂解会损害脑源性神经营养因子(BDNF)信号转导,从而损害神经元的存活、分化以及突触传递和可塑性。通过使用脑脊液和死后的人脑样本,我们发现 TrkB-FL 的裂解发生在疾病的早期阶段,并随着病理严重程度的增加而增加。为了探索这种疾病机制的治疗潜力,我们设计了小的 TAT 融合肽,并筛选了它们预防 TrkB-FL 受体裂解的能力。在这些肽中,带有赖氨酸-赖氨酸连接子的 TAT-TrkB 肽可在体外和体内防止 TrkB-FL 的裂解,并挽救寡聚 Aβ在海马切片中诱导的突触缺陷。此外,这种 TAT-TrkB 肽可改善认知表现、改善突触可塑性缺陷并预防 5XFAD 型 AD 小鼠模型中的 Tau 病理进展。未发现肝或肾毒性的证据。我们提供了这种治疗策略的疗效和安全性的概念验证证据,并预计这种 TAT-TrkB 肽具有成为一种疾病修饰药物的潜力,可以预防和/或逆转 AD 患者的认知缺陷。