Functional and gene expression analysis of hTERT overexpressed endothelial cells

Abstract

Telomerase dysfunction contributes to cellular senescence. Recent advances indicate the importance of senescence in maintaining vascular cell function in vitro. Human telomerase reverse transcriptase (hTERT) overexpression is thought to lead to resistance to apoptosis and oxidative stress. However, the mechanism in endothelial lineage cells is unclear. We tried to generate an immortal endothelial cell line from human umbilical vein endothelial cells using a no-virus system and examine the functional mechanisms of hTERT overexpressed endothelial cell senescence in vitro. High levels of hTERT genes and endothelial cell-specific markers were expressed during long-term culture. Also, angiogenic responses were observed in hTERT over-expressed endothelial cell. These cells showed a delay in senescence and appeared more resistant to stressed conditions. PI3K/Akt-related gene levels were enhanced in hTERT overexpressed endothelial cells. An up-regulated PI3K/Akt pathway caused by hTERT overexpression might contribute to anti-apoptosis and survival effects in endothelial lineage cells.

Keywords:

• endothelial
• telomerase
• senescence
• oxidative stress
• anti-apoptosis
• PI3K/Akt pathway

Acknowledgements

We appreciate Dr. Hiromi Nishimura for providing the human umbilical cord samples, and Dr. Masakazu Ishikawa for technical support in part of RT-PCR primers.

Disclosures

None of the authors have any conflicts of interest to disclose.