Does telomerase protein protect our neurons?

Gabriele C Saretzki

Institute for Cell and Molecular Biosciences, Newcastle Institute for Ageing, Campus for Ageing and Vitality, Newcastle University, UK

Telomerase is best known for its canonical function in telomere maintenance. However, a growing number of non-telomeric functions have been described. Several groups have found the telomerase protein TERT to persist in adult brain neurons. A protective role for the telomerase protein TERT had been demonstrated in cultivated mouse neurons during brain development, against excitotoxic stresses from N-methyl-D-aspartate (NMDA) and glutamate and agents known to be involved in neurodegenerative diseases such as beta amyloid peptides and hyperphosphorylated tau. In contrast, lack of telomerase and TERT protein increase oxidative stress and decrease neuronal survival. Research on telomerase and TERT protein in human neurodegenerative diseases is a relatively new field. However, there is emerging evidence of a beneficial role of telomerase in human brains and animal models of neurodegenerative diseases that suggests to explore the possibility of using telomerase activators as neuroprotective agents to combat brain ageing and to ameliorate neurodegenerative diseases such as Parkinson’s and Alzheimer’s diseases. The current mini-review summarises the knowledge about this developing novel area of brain research.

 Telomerase is a reverse transcriptase best known as the enzyme that extends and maintains telomeres, the protective ends of linear chromosomes, in dividing cells. It consists of the catalytic protein TERT (Telomerase Reverse Transcriptase) and an RNA subunit which contains the template region for telomere synthesis. However, in most human somatic cells telomerase is downregulated early during development1,2 while some cell types such as endothelial cells, lymphocytes and adult stem cells express some activity throughout life. Due to its own RNA moiety, telomerase is able to extend the 3’ overhang of telomeres, generated during DNA replication and thus counteract telomere shortening. Without sufficient telomerase activity present, telomeres shorten due to the inability of conventional DNA polymerases to replicate the lagging strand at the end of chromosomes, the so called “end replication problem”3,4. Importantly, also oxidative stress has been shown to be a major reason for telomere shortening5. However, telomere shortening happens mainly in dividing cells and this division is required for translating accumulated DNA damage and DNA breaks into telomere shortening6. In addition, telomeres are not well repaired7. DNA damage however, can also happen in non-dividing cells such as neurons and it was even shown that the grade of maturation might play a role with newly formed neurons possibly more sensitive against DNA damage than mature ones8. Whether and to what extent all neuron types and brain areas are prone to DNA damage remains a research question still under debate9. In some neuron types such as Purkinje neurons, both DNA damage and cellular senescence as well as telomerase have been detected10-12.

The research on the involvement of telomerase in neurons and the brain was pioneered by Mark Mattson’s group more than 15 years ago. They showed that cultivated neurons from mouse embryos need telomerase activity for protection and development and that telomerase promotes their survival against trophic factor withdrawal, glutamate-induced excitotoxicity and amyloid peptides in cultured mouse primary neurons13-16. Analysing telomerase activity as well as the expression of its protein part TERT it became apparent that, while telomerase activity is downregulated early during brain development in humans1 and postnatally in rodents, the TERT protein seemed to persist even in adult mouse brains17,18.

In addition to telomere-dependent, canonical functions of telomerase, more and more telomere-independent, non-canonical functions of the TERT protein became apparent over the last decade (for reviews see19,20). This includes subcellular shuttling of TERT from the nucleus to mitochondria upon increased oxidative stress21-24. In addition to a nuclear localisation signal (NLS) and a nuclear exclusion signal (NES)25,26 TERT in higher organisms such as mammals, also contains a specific mitochondrial localisation signal (MLS)21. The nuclear exclusion upon oxidative stress is dependent on Src kinase and Ran GTPase27. TERT within mitochondria exerts a protective function with a decrease of mitochondrial and intracellular oxidative stress, decrease of apoptosis and protection of mitochondrial and nuclear DNA22-24 although the exact underlying mechanisms still remain elusive. Binding to mitochondrial DNA, improvement of mitochondrial respiration and changes in cellular antioxidants have been suggested23,28,29. Interestingly, Santos’ group demonstrated that the TERT protein can exert its reverse transcriptase function in mitochondria by using mitochondrial tRNAs as templates for reverse transcription29 although the biological significance of that novel catalytic function of telomerase within mitochondria has not been demonstrated yet. There is an ongoing debate in the telomerase field whether some non-canonical functions are dependent on the presence of the catalytic function of TERT while others are not (for review see 20). Demonstrating the catalytic function of TERT within mitochondria does not answer this question since no direct correlation between the catalytic activity of TERT in mitochondria and its protective function has been confirmed. It is also not known whether catalytic activity of TERT is essential or required for the protection of neurons by TERT. The protective role of mammalian TERT in mitochondria has recently been demonstrated even in yeast where it increased the resistance against oxidative stress without interacting with telomeres or the yeast TERT which lacks the mitochondrial localisation signal30.

Our group also found that upon treatment with hydrogen peroxide or irradiation cancer cells exclude TERT protein in a heterogeneous manner and intriguingly, nuclear DNA damage correlated positively with TERT protein remaining within the nucleus; while cells with cytoplasmic/mitochondrial TERT localisation had lower nuclear DNA damage, lower levels of reactive oxygen species (ROS) and hardly any apoptosis. In contrast, cells with a nuclear TERT localisation had high amounts of DNA damage, oxidative stress as well as apoptosis24. This finding corresponds well with results from experiments that used a hTERT protein with a mutant NES rendering the protein unable to leave the nucleus resulting in increased nuclear and mitochondrial DNA damage as well as higher levels of oxidative stress32,33.

There are various mechanisms of neuronal cell death in the brain during neurodegeneration. While in Parkinson’s disease (PD) apoptosis might occur as the pre-dominant mechanism, in Alzheimer’s disease (AD) the exact mechanism of neuronal degeneration is still not known31. Consequently, the involvement of TERT into neuronal apoptosis has not been investigated yet.

It has not been analysed in detail whether nuclear localisation of TERT is the default situation in all cell types. Immune cells such as lymphocytes have their TERT protein in the cytoplasm under unstimulated conditions and transport it into the nucleus upon antigen or inflammatory stimulation (see Figure 1 A) and activate telomerase activity and nuclear translocation by phosphorylating TERT on serine 227 by AKT34-36. In contrast, it is thought that TERT and telomerase activity are localised within the nucleus under non-stressed conditions24 (see Figure 1B). Intriguingly, Iannilli et al showed that in fully differentiated neurons the majority of cytoplasmic TERT forms a complex with RNA granules and binds to the mRNA of p15INK4b, a pro-survival cell cycle inhibitor37. Upon cellular stress TERT and p15 dissociated resulting in translation of p15 while TERT was free to shuttle to mitochondria. The authors also showed that the anti-apoptotic functions of TERT and p15 in cultivated rat hippocampal neurons were mutually dependent on each other37. In general, Iannilli’s findings suggested that TERT protein is not necessarily localised in the nucleus of neurons corresponding to reports from Spilsbury et al.38 who also found TERT signals predominantly outside the nucleus in hippocampal human and cultivated mouse neurons although contradicting results exist and changes might occur with the age of the organism10.

Mattson’s group also showed that presence of telomerase is able to protect against apoptosis, withdrawal of growth factors and glutamate treatment (excitotoxicity) as well as treatment with amyloid precursor protein in cultivated primary mouse neurons13,16. Thus, a potential connection between the presence of TERT protein in adult brains and neurodegeneration was possible39. Recently, Esther Priels’ group has demonstrated that boosting telomerase levels in mice by using specific compounds that activate telomerase, can ameliorate NMDA toxicity in wild type mice40. This seems to correspond well to a previous study in mouse brains in vivo that showed that overexpressing TERT in neurons did not result in any telomerase activity but improved protection of neurons from NMDA excitotoxicity as well as mitochondrial functions such as mitochondrial membrane potential41. Importantly, Eitan and co-workers also showed that compounds that activate telomerase can ameliorate symptoms and disease severity in a mouse model of Amyotrophic Lateral Sclerosis (ALS), again suggesting a beneficial effect of telomerase/TERT levels in the brain of adult mice of a neurodegenerative mouse model40.

It had been demonstrated that telomerase activity is downregulated very early during human brain development1. However, not much research had been performed on adult human brains. Our group used human brain tissue from the Newcastle Brain Tissue Resource (NBTR) and analysed the hippocampus of donors with different Braak stages of Alzheimer’s disease (AD) and compared them to age-matched healthy controls. We found that only neurons, but not astrocytes expressed any TERT protein while there was some expression in human microglia, presumably due to their nature being macrophages38. While our initial hypothesis was that TERT protein might decrease due to disease progression, we could not find any evidence of that using different techniques such as Western blotting and immuno-fluorescence staining for TERT protein38. However, we found that there was a significant increase in the amount of mitochondrial TERT localisation in hippocampal areas CA1-3 of advanced AD cases (Braak stage 6) compared to healthy controls (Braak stage 0). Oxidative stress and mitochondrial dysfunction increase during brain ageing and are suggested to be involved in the pathogenesis of Alzheimer’s disease (AD) and other neurodegenerative diseases. In both AD and animal models of neurodegenerative diseases, chronically increased oxidative stress levels have been found to represent one of the earliest changes before specific pathologies such as amyloid-β (Aβ) plaques and neurofibrillary tangles occur42,43. Our findings together with that of Iannilli et al.37 suggest that TERT protein enters neuronal mitochondria from the cytoplasm due to increased oxidative stress where it might exert a protective function (see Figure 1C). This suggestion is also supported by our results of a lack of co-localisation of hyperphosphorylated tau protein (either as neuropil threads or neurofibrillary tangles) and TERT protein in human hippocampi of advanced Braak stages in AD brains where we found a mutual exclusion of both proteins: neurons expressing TERT did not show any tau pathology while cells with neuropil threads or neurofibrillary tangles did not show any TERT expression38. Whether high TERT expression was really protective against hyperphosphorylated tau or tau expressing neurons did displace or downregulate TERT can only be speculated at that point. However, in order to model tau pathology in an experimental system we used cultivated mouse embryonic neurons from both wild type as well as TERT knockout mice (first generation with no effect on telomere length). Similar to human brains, we found that only neurons, but not astrocytes expressed any TERT protein. Measuring oxidative stress we found that neurons lacking the TERT protein (from first generation TERT knock-out mice44) had higher levels of ROS after an oxidative challenge while there were no significant differences before the treatment. This finding corresponds well to that from Iannilli et al. 37 and suggests that only under stressed conditions the better protection of neurons expressing TERT might become evident due to its localisation to mitochondria. Indeed, we found an increased amount of TERT protein localised to mitochondria in wild type neurons after applying oxidative stress compared to basal unstressed conditions. Transducing wild type and TERT knock-out neurons (at a time point when in wild type neurons telomerase activity was already downregulated while the TERT protein persisted) with mutated human tau protein (P301L mutation known from human tauopathies45), we found that neurons from TERT knock-out mice had significantly more mitochondrial ROS in dendrites, but not in the cell body. Similarly, we found more peroxidised lipids in neurons lacking TERT protein, but this time the difference was significant in the cell bodies, presumably due to a higher lipid content there38. Our data on mitochondrial localisation of TERT in neurons are in accordance with those from Eitan et al.11 who recently also demonstrated that glutamate-induced excitotoxicity stress increased the amount of TERT protein within mitochondria in mouse Purkinje neurons supporting the idea of dynamic changes in subcellular localisation of TERT due to physiological as well as pathological processes.

Other groups used TERT knock-out mice to demonstrate that lack of TERT increased infarct volumes, stroke-related neuro-inflammation, as well as enhanced behavioural abnormalities such as anxiety at higher age17,46. However, in these studies on whole brains and organisms it is not entirely clear whether it was neuronal TERT or rather TERT protein in vascular endothelial cells that contributed to the phenotype. Additional aspects of the beneficial effects of telomerase in the central nervous system have been summarised in a current review47.

Taken together, there is growing evidence for a cytoplasmic localisation of TERT protein in adult neurons that seems to correlate to a protective function in the brain that is quite distinct from telomerase enzymatic activity on telomeres. Consequently, these results suggest that an increase of TERT protein at higher age might help to prevent or ameliorate brain ageing as well as the onset and progression of various neurodegenerative diseases. Thus, telomerase might be viewed as a novel target for future strategies to combat neurodegenerative diseases. First results on mouse models of neurodegeneration are encouraging but have to be scrutinised carefully in a human setting.

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Article Info

  • Journal of Neurology & Neuromedicine
  • Article Type : Mini Review
  • View/Download pdf
  • DOI : 10.29245/2572.942X/2016/2.1025

Article Notes

  • Published on: May 18, 2016


  • neurodegenerative

  • hyperphosphorylated
  • telomerase


Dr. Gabriele C Saretzki
Institute for Cell and Molecular Biosciences, Newcastle Institute for Ageing, Campus for Ageing and Vitality, Newcastle University Newcastle upon Tyne, NE4 5PL, UK
Telephone: +44 191 2081214, Fax: +44 191 2081101
Copyright: ©2016 G Saretzki . This article is distributed under the terms of the Creative Commons Attribution 4.0 International License.
Citation: G Saretzki. Does telomerase protein protect our neurons?. J Neurol Neuromed (2016) 1(2): 23-28