García Porta Cloe, Mahfooz Kashif, Komorowska Joanna, Garcia-Rates Sara, Greenfield Susan
Neuro-Bio Ltd., Building F5, Culham Science Centre, Abingdon OX14 3DB, UK.
Int J Mol Sci. 2024 Nov 29;25(23):12837. doi: 10.3390/ijms252312837.
During development, a 14mer peptide, T14, modulates cell growth via the α-7 nicotinic acetylcholine receptor (α7 nAChR). However, this process could become excitotoxic in the context of the adult brain, leading to pathologies such as Alzheimer's disease (AD). Recent work shows that T14 acts selectively via the mammalian target of rapamycin complex 1 (mTORC1). This pathway is essential for normal development but is overactive in AD. The triggering of mTORC1 has also been associated with the suppression of autophagy, commonly observed in ageing and neurodegeneration. We therefore investigated the relationship between T14 and autophagic flux in tissue cultures, mouse brain slices, and human Alzheimer's disease hippocampus. Here, we demonstrate that T14 and p-mTOR s2448 expression significantly increases in AD human hippocampus, which was associated with the gradual decrease in the autophagosome number across Braak stages. During development, the reduction in T14 positively correlated with pTau (Ser202, Thr205) and two selective autophagy receptors: p62 and optineurin. In vitro studies also indicated that T14 increases p-mTOR s2448 expression, resulting in the aggregation of polyubiquinated substances. The effective blockade of T14 via its cyclic variant, NBP14, has been validated in vitro, in vivo, and ex vivo. In this study, NBP14 significantly attenuated p-mTOR s2448 expression and restored normal autophagic flux, as seen with rapamycin. We conclude that T14 acts at the α-7 receptor to selectively activate the mTORC1 pathway and consequently inhibit autophagic flux. Hence, this study describes a further step in the process by which T14 could drive neurodegeneration.
在发育过程中,一种14肽T14通过α-7烟碱型乙酰胆碱受体(α7 nAChR)调节细胞生长。然而,在成人大脑的背景下,这个过程可能会变得具有兴奋性毒性,导致诸如阿尔茨海默病(AD)等病理状况。最近的研究表明,T14通过雷帕霉素靶蛋白复合物1(mTORC1)选择性发挥作用。该途径对正常发育至关重要,但在AD中过度活跃。mTORC1的激活还与自噬抑制有关,这在衰老和神经退行性变中很常见。因此,我们在组织培养、小鼠脑片和人类阿尔茨海默病海马体中研究了T14与自噬通量之间的关系。在这里,我们证明在AD人类海马体中T14和磷酸化mTOR(s2448)的表达显著增加,这与Braak分期中自噬体数量的逐渐减少有关。在发育过程中,T14的减少与磷酸化tau蛋白(Ser202,Thr205)以及两种选择性自噬受体:p62和视黄醇结合蛋白呈正相关。体外研究还表明,T14增加了磷酸化mTOR(s2448)的表达,导致多聚泛素化物质的聚集。通过其环状变体NBP14对T14的有效阻断已在体外、体内和离体实验中得到验证。在本研究中,NBP14显著减弱了磷酸化mTOR(s2448)的表达,并恢复了正常的自噬通量,这与雷帕霉素的作用效果相似。我们得出结论,T14作用于α-7受体以选择性激活mTORC1途径,从而抑制自噬通量。因此,本研究描述了T14引发神经退行性变过程中的又一步骤。