Telomerase Reverse Transcriptase Preserves Neuron Survival and Cognition in Alzheimer's Disease Models.

Abstract

Amyloid-induced neurodegeneration plays a central role in Alzheimer's disease (AD) pathogenesis. Here, we show that <i>telomerase reverse transcriptase (TERT)</i> haploinsufficiency decreases BDNF and increases amyloid-β (Aβ) precursor in murine brain. Moreover, prior to disease onset, the <i>TERT</i> locus sustains accumulation of repressive epigenetic marks in murine and human AD neurons, implicating <i>TERT</i> repression in amyloid-induced neurodegeneration. To test the impact of sustained <i>TERT</i> expression on AD pathobiology, AD mouse models were engineered to maintain physiological levels of TERT in adult neurons, resulting in reduced Aβ accumulation, improved spine morphology, and preserved cognitive function. Mechanistically, integrated profiling revealed that TERT interacts with β-catenin and RNA polymerase II at gene promoters and upregulates gene networks governing synaptic signaling and learning processes. These TERT-directed transcriptional activities do not require its catalytic activity nor telomerase RNA. These findings provide genetic proof-of-concept for somatic <i>TERT</i> gene activation therapy in attenuating AD progression including cognitive decline.