Telomeres are elongated in rats exposed to moderate altitude
- Yaping Wang†1,
- Wen-di Zhou†2,
- Yingzhong Yang1,
- Lan Ma1,
- Yanxia Zhao1,
- Zhenzhong Bai1 and
- Ri-Li Ge1, 3Email author
© Wang et al.; licensee BioMed Central Ltd. 2014
Received: 7 May 2014
Accepted: 20 June 2014
Published: 4 July 2014
Leukocyte telomere length has been shown to be associated with life span. Hypoxia-associated changes of telomere length have been detected in cell cultures, but no in vivo studies have reported the changes of telomere length under different hypoxic conditions. This study aimed to evaluate the effects of altitude on telomere length in rat leukocytes.
One hundred and ten male Wistar rats were randomized into 3 groups and maintained at sea-level (altitude of 10 m) (SL group, n = 10), moderate altitude (2,260 m) (MA group, n = 50), or simulated high altitude (5,000 m (SHA group, n = 50). The last two groups were further divided into 5 subgroups and exposed to hypoxia for 1, 3, 7, 15, or 30 days (n = 10). The leukocyte telomere length, hemoglobin concentration, red blood cell count, hematocrit, and plasma levels of telomerase reverse transcriptase (TERT), hypoxia-inducible factor 1α (HIF-1α), malondialdehyde (MDA) and superoxide dismutase (SOD) were measured.
Leukocyte telomere length was significantly longer in the MA group than in the SL or SHA groups, and the TERT expression changed in a similar manner as the leukocyte telomere length. However, HIF-1α level was significantly higher in both MA and SHA groups than the SL group. SOD level was decreased and MDA level was elevated in SHA group.
The telomere length of blood leukocytes is elongated at a moderate altitude, but not at a high altitude. A mild hypoxic state may increase telomere length.
KeywordsTelomere Altitudes Hypoxia-inducible factor 1α Superoxide dismutase Malondialdehyde
Telomeres are specialized nucleoprotein structures at the ends of chromosomes that are composed of thousands of TTAGGG/AATCCC repeats and associated proteins . A critical function of telomeres is to cap and protect the ends of chromosomes from degradation and end-to-end fusions, which otherwise would result in the loss of genetic information and chromosomal instability . It has been well established that excessive shortening of the telomeres can lead to genomic instability or activation of cellular damage responses, such as cellular senescence and apoptosis . Telomeres are also essential for cell survival and replicative capacity of dividing somatic cells.
Telomere shortening occurs as a consequence of the proliferation along with each cell division. Increasing evidence indicates the association between the significant telomere shortening of hepatocytes and the replicative senescence of a non-dividing state . Leukocyte telomere length was shown to be positively related to life span, thereby making it a potential indicator of longevity . Recent studies have shown that a number of factors have effects on the telomere length in somatic cells, including low temperature, ultraviolet radiation, smoking, diet, mental stress, inflammation and oxidative stress [6–11]. A topic of increasing importance in recent years concerns the role of hypoxia. Telomere length has been shown to vary considerably among different hypoxia levels and cell types [12–14]. However, most of these studies are in vitro, and few studies have investigated the effects of hypoxia on telomere length in vivo.
In this study, we measured the telomere lengths of peripheral blood leukocytes in the rats exposed to different altitudes (10 m, 2,260 m, 5,000 m) for different periods (1, 3, 7, 15, 30 days), with the aim to elucidate the effect of altitude and hypoxia on aging.
All animal experiments were approved by the Ethical Committee of Qinghai University. A total of 110 male Wistar rats (approximately 150 to 180 g) were used in this study. All the rats were maintained in a controlled environment at 18 to 20°C with unlimited access to food and water on a 12-hour light/dark cycle, and then randomized into one of the following three groups. In the sea-level (SL) group, ten rats were maintained in Nanjing where the altitude was about ten meters. In the moderate altitude (MA) group, 50 rats were transported from Nanjing to Xining where the altitude was about 2,260 m, and further divided randomly into the 1-, 3-, 7-, 15-, 30-day subgroups (MA 1, 3, 7, 15, 30), with 10 rats in each subgroup. In the simulated high altitude (SHA) group, 50 rats were put into a hypobaric chamber in Xining where an altitude of 5,000 m was simulated, and further divided randomly into the 1-, 3-, 7-, 15-, 30-day subgroups (SHA 1, 3, 7, 15, 30), with 10 rats in each subgroup.
Measurement of hemoglobin (HGB), red blood cell count (RBC) and hematocrit (HCT)
Venous blood was taken from the rats and HGB, RBC and HCT were measured using an automatic blood cell analyzer (BC-2300, Mairui Biotec, Wuhan, China) following the manufacturer's instruction.
DNA isolation and quantitative PCR
Genomic DNA was isolated from peripheral blood leukocytes using a Blood DNA extraction kit (Tiangen Biotech, Beijing, China) following the manufacturer’s instruction, and dissolved in TE buffer (pH 8.0) at the concentration of 25 ng/μl. Quantitative PCR was performed using the SYBR® Select Master Mix (Takara, Dalian, China) with an ABI PRISM 7500 (Applied Biosystems, Foster City, CA, USA). The parameters were as follows: 95°C for 30 seconds, followed by 40 cycles of 95°C for 5 seconds and 60°C for 34 seconds. Primers used were as follows: Tel-1 5’GGT TTT TGA GGG TGA GGG TGA GGG TGA GGG TGA GGG t-3’, and Tel-2 5’-TCC CGA CTA TCC CTA TCC CTA TCC CTA TCC CTA TCC CTA-3’; AT1 rat-f 5’-ACG TGT TCT CAG CAT CGA CCG CTA CC-3’ and AT1 rat-r 5’-AGA ATG ATA AGG AAA GGG AAC AAG AAG CCC-3’ (Invitrogen, Carlsbad, CA, USA). The quantities of telomeric DNA were normalized to that of AT1. The relative telomere length was determined by calculating the relative ratio of telomere (T) and single gene copy AT 1 receptor (S), expressed as T/S ratio.
Plasma levels of TERT, HIF-1α, SOD and MDA
The plasma samples were separated from the blood. The plasma levels of telomerase reverse transcriptase (TERT) and hypoxia-inducible factor 1α (HIF-1α) were detected using an ELISA kit (USCN Life Science Inc., Atlanta, GA, USA), and the plasma levels of superoxide dismutase (SOD) and malondialdehyde (MDA) were detected by WST-1 and TBA assay (SOD and MDA kit, Jiancheng Biotech Ltd., Nanjing, China) according to the manufacturer’s protocols.
All data were presented as mean ± SD and analyzed using the SPSS version 12 statistical analysis package (SPSS Inc., Chicago, IL, USA). Statistical analysis was performed by one-way ANOVA, followed post hoc test. P-values less than 0.05 were considered statistically significant.
Hematological changes in rats exposed to different altitude
Telomere length of leukocytes from rats exposed to different altitude
Plasma levels of TERT, HIF-1α, SOD and MDA in rats exposed to different altitude
To our knowledge, this is the first in vivo study that compared leukocyte telomere length of rats exposed to different hypoxic conditions. Our results showed that the telomeres were significantly elongated in a mildly rather than highly hypoxic environment, and that the expression of TERT and HIF-1α changed in a similar manner as the leukocyte telomere length under the hypoxic conditions.
Telomere length is known to be maintained by telomerase, a specialized ribonucleoprotein complex consisting of a catalytic protein subunit TERT and a telomerase RNA component (TERC) that serves as a template for telomere extension during de novo addition of TTAGGG repeats onto chromosome ends . TERT expression parallels telomerase activity in many multicellular organisms, indicating that telomerase activity can be determined indirectly by measuring TERT expression [15, 16]. Exposure to hypoxia has been shown to activate telomerase due to its ability to increase TERT expression, which in turn results in telomere elongation [17, 18]. The mechanisms responsible for hypoxia-induced TERT expression have been investigated, and it was shown that TERT expression was upregulated following the induction of HIF-1α during exposure to hypoxia and HIF-1α acted as an essential transactivator to induce TERT transcription [19–21].
Our results showed that the general condition of rats exposed to moderate hypoxia were good and without significant oxidative damage. However, the level of the antioxidant enzyme SOD declined and the oxide metabolite MDA gradually elevated in the SHA group, which suggests that antioxidative stress activity is decreased in the rats and renders them susceptible to oxidant injury. Previous studies have shown that severe hypoxia (low oxygen tension) can damage cellular components by producing ROS through the oxidation of DNA, proteins and lipids. Oxidative stress preferentially damages telomeric DNA regions and inhibits telomerase activity in vitro in various cell types, and has been suggested as a major cause of telomere shortening [22–25]. Therefore, it is possible that under severe hypoxic conditions oxidative stress-associated telomere DNA damage may counteract the increased telomerase activity and telomere elongation induced by HIF-1α.
In this study, HIF-1α expression was lower in the SHA group than in the MA group. It has been reported that increased production of ROS could downregulate HIF-1α, and impair the adaptive response of many oxygen-sensitive genes to hypoxia . Interestingly, we found that the changes of HIF-1α and TERT expression and telomere length were correlated with the duration of exposure to hypoxia in both the MA and SHA groups. In general, HIF-1α and TERT expression and telomere length were increased on the first day of exposure to the hypoxic environment and then decreased rapidly to a stable level with further exposure. These results are consistent with previous findings that HIF-1α expression could be increased by acute hypoxia, but chronic exposure to hypoxia induced the downregulation of HIF-1α expression [27, 28]. Notably, we observed that in the MA group telomere length was significantly elongated on the first day but was then markedly reduced afterwards, indicating that telomere length may be adapted after exposure to hypoxia.
Our study showed that the telomeres of peripheral blood leukocytes were elongated at moderate altitude, but not at high altitude, and the telomere length was related to the periods of exposure to hypoxic environment. Furthermore, we found that HIF-1α and TERT expression and oxidative stress damage were parallel to the changes of telomere length. These findings support the beneficial effects of mild stress . However, further studies are needed to explore alternative possibilities and elucidate the relationship between leukocyte telomere length and longevity in humans living at different altitudes.
simulated high altitude
telomerase reverse transcriptase
hypoxia-inducible factor 1α
superoxide dismutase (SOD).
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