Glucose derived carbon nanosphere (CSP) conjugated TTK21, an activator of the histone acetyltransferases CBP/p300, ameliorates amyloid-beta 1-42 induced deficits in plasticity and associativity in hippocampal CA1 pyramidal neurons

葡萄糖衍生的碳纳米球 (CSP) 结合 TTK21(组蛋白乙酰转移酶 CBP/p300 的激活剂),可改善淀粉样蛋白-β 1-42 引起的海马 CA1 锥体神经元的可塑性和联想性缺陷

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作者:Akash K Singh, Sin H Neo, Christine Liwang, Karen K L Pang, Jason C K Leng, Sarmistha H Sinha, Mahesh S Shetty, Madavan Vasudevan, Vinay J Rao, Ila Joshi, Muthusamy Eswaramoorthy, Maria V Pavon, Ang R Sheila, Sheeja Navakkode, Tapas K Kundu, Sreedharan Sajikumar

Abstract

The master epigenetic regulator lysine acetyltransferase (KAT) p300/CBP plays a pivotal role in neuroplasticity and cognitive functions. Recent evidence has shown that in several neurodegenerative diseases, including Alzheimer's disease (AD), the expression level and function of p300/CBP are severely compromised, leading to altered gene expression causing pathological conditions. Here, we show that p300/CBP activation by a small-molecule TTK21, conjugated to carbon nanosphere (CSP) ameliorates Aβ-impaired long-term potentiation (LTP) induced by high-frequency stimulation, theta burst stimulation, and synaptic tagging/capture (STC). This functional rescue was correlated with CSP-TTK21-induced changes in transcription and translation. Mechanistically, we observed that the expression of a large number of synaptic plasticity- and memory-related genes was rescued, presumably by the restoration of p300/CBP mediated acetylation. Collectively, these results suggest that small-molecule activators of p300/CBP could be a potential therapeutic molecule for neurodegenerative diseases like AD.

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