Endoplasmic reticulum stress activates telomerase

Telomerase contributes to cell proliferation and survival through both telomere-dependent and telomere-independent mechanisms. In this report, we discovered that endoplasmic reticulum (ER) stress transiently activates the catalytic components of telomerase (TERT) expression in human cancer cell lines and murine primary neural cells. Importantly, we show that depletion of hTERT sensitizes cells to undergo apoptosis under ER stress, whereas increased hTERT expression reduces ER stress-induced cell death independent of catalytically active enzyme or DNA damage signaling. Our findings establish a functional link between ER stress and telomerase, both of which have important implications in the pathologies associated with aging and cancer.

Human telomerase is a ribonucleoprotein enzyme complex that is minimally composed of a RNA component (hTR or hTERC) and the telomerase reverse transcriptase (hTERT; Blackburn, 2000). Telomerase has fundamental roles in aging and in cancer (Artandi, 2006). However, the pathways and molecular mechanisms regulating telomerase remain poorly understood. Importantly, telomerase appears to have telomereindependent functions in a number of fundamental cellular processes (Cong & Shay, 2008). The endoplasmic reticulum (ER) is a cytosolic membrane network connected to the nucleus, mitochondria, and the plasma membrane (Tabas & Ron, 2011). The ability to respond to perturbations in ER function (ER stress) is a fundamental important property of cells (Wang & Kaufman, 2012).
We sought to investigate the expression and function of telomerase in ER stress responses. In HeLa and MCF7 cells, treatment with thapsigargin (Tg) or ionomycin (In) induced ER stress responses characterized by increased specific expression of Bip, IRE1a, CHOP, and XBP-1 (Fig. 1A). Interestingly, we found that hTERT protein and hTERT mRNA expression was up-regulated 1 h after the Tg or In treatment, which then decreased 8 h post-treatment (Figs 1A,B and S1A). No changes were observed in the levels of hTR, (data not shown). Additionally, the expression of hTERT was increased in MCF7 cells under different ER stress conditions (Fig.  S1B). As another proof that hTERT protein levels are increased under ER stress, we showed that the telomerase enzymatic activity in vitro was also increased (Figs 1C and S1C). Importantly, treatment with Tg dramatically increased the mTERT mRNA expression in primary mouse CGN and NPC cells (Figs 1D and S2). Control treatment with DMSO in HeLa, MCF7, and CGN cells has no effect on either ER stress induction or TERT up-regulation (Fig. S3). These results suggest that up-regulation of TERT under ER stress may represent a bona fide cellular process involved in the ER stress response.
We then investigated potential roles of TERT against ER stress-induced cell death. As shown in Fig. 2, treatment with Tg induced apoptotic cell death in MCF7 cells. However, the depletion of hTERT by four hTERTspecific On-Target plus siRNA oligos (Dharmacon) potentiated cell death of MCF7 cells under ER stress ( Fig. 2A). The depletion of hTERT expression also increased Tg-induced cytotoxicity in MCF7 cells (Fig. 2B). Conversely, in U2OS cells that lack telomerase expression, infection of lenti-hTERT or lenti-K626A, a catalytically inactive mutant hTERT K626A (Weinrich et al., 1997), significantly inhibited cell death (Fig. 2C) and reduced cytotoxicity under Tg-induced ER stress (Fig. 2D). Together, these results indicated that increased expression of hTERT suppresses the ER stress-induced cell death independently of catalytic active telomerase enzyme.
We next tested if ER stress induced DNA damage response and subsequently activated telomerase. Our results indicated that ER stress under our assay conditions did not result in DNA damage responses (Fig.  S4). Given that hTERT was up-regulated as early as 1 h after ER stress induction and decreased at 8 h postinduction, we therefore conclude that the anti-apoptosis effect of increased hTERT expression under ER stress may be independent of telomere maintenance.
hTERT was up-regulated immediately upon ER stress induction, suggesting transcriptional regulation. It is known that the ER stress pathway triggers activation of the transcription factor NF-jB (Hung et al., 2004) and that the transcription factor NF-jB has been implicated with the regulation of hTERT transcription (Sinha-Datta et al., 2004). We then investigated whether NF-jB was involved in up-regulation of hTERT expression under ER stress. We observed that ER stress increased nuclear translocation of the NF-jB p65 transcription factor, which correlated with a concomitant decrease in the IjBa levels and an increase in the NF-jB reporter activity (Fig. S5). However, the transfection of the IjBa super-repressor (IjBa-SR), an efficient NF-jB inhibitor (Reuther et al., 1998), inhibited the ER stress-induced hTERT up-regulation (Fig. S6A). Similarly, ER stressinduced hTERT up-regulation was compromised in the presence of the specific NF-jB inhibitor PDTC (Fig. S6B). These results indicate that the NF-jB pathway may be required for up-regulation of hTERT under ER stress.
TERT is expressed at high levels during the process of neuronal differentiation and then decreases sharply during the period when programmed cell death occurs (Fu et al., 2000). Importantly, suppression of TERT expression promotes apoptosis of neurons, whereas overexpression of TERT suppresses apoptosis (Fu et al., 2000). Additionally, fully differentiated neurons and astrocytes do not express telomerase activity, but the expression of TERT increased in response to oxidative stress, amyloid b-peptide-induced damage and ischemia-induced neurotoxicity (Saretzki, 2009). These observations suggest that deregulation of TERT expression due to genetic or epigenetic alterations in the adult brain may contribute to the vulnerability in age-related neurodegenerative disorders. In contrast, cancer cells frequently experience ER stress as may provide molecular insights into the mechanisms associated with ER stress-related disease.

Supporting Information
Additional Supporting Information may be found in the online version of this article at the publisher's web-site.      ER stress activates telomerase, J. Zhou et al.