Peptide Epitalon Activates Telomerase Activity and Elongates Telomeres in Human Somatic Cells
Khavinson V.H., Bondarev I.E., Butyugov A.A.
St. Petersburg Institute of Bioregulation and Gerontology
Introduction
Telomere shortening is a primary mechanism of cellular aging (the Hayflick limit). Telomerase is the enzyme capable of rebuilding telomeres. This study investigated if the tetrapeptide Epitalon (Ala-Glu-Asp-Gly) could activate telomerase.
Experimental Design
Human fetal lung fibroblast cells were cultured. Epitalon was added to the culture medium. Telomere length was measured using the TRF (Terminal Restriction Fragment) assay.
Key Findings
Telomerase Activation
Epitalon induced telomerase activity in somatic cells that normally do not express it. This is a groundbreaking finding for a small molecule.
Telomere Elongation
Cells treated with Epitalon showed a 33.3% increase in mean telomere length compared to controls.
Cell Lifespan
The treated cells exceeded their normal Hayflick limit, undergoing significantly more population doublings while maintaining a normal karyotype (no cancer-like changes).
Significance
This study provides the cellular mechanism for the life-extension effects observed in animal and human studies: Epitalon acts as a gene switch to activate the telomerase gene.
Key Findings
- ✓Epitalon activates the telomerase enzyme
- ✓Telomeres elongated by 33.3%
- ✓Extended cellular replicative lifespan
Mechanism of Action
Epitalon upregulates the expression of the TERT gene (Telomerase Reverse Transcriptase) via specific binding to DNA in the promoter region.