1. Academic Validation
  2. Novel vaccine peptide GV1001 effectively blocks β-amyloid toxicity by mimicking the extra-telomeric functions of human telomerase reverse transcriptase

Novel vaccine peptide GV1001 effectively blocks β-amyloid toxicity by mimicking the extra-telomeric functions of human telomerase reverse transcriptase

  • Neurobiol Aging. 2014 Jun;35(6):1255-74. doi: 10.1016/j.neurobiolaging.2013.12.015.
Hyun-Hee Park 1 Kyu-Yong Lee 1 Sangjae Kim 2 Jessica Woojin Lee 2 Na-Young Choi 3 Eun-Hye Lee 3 Young Joo Lee 1 Sang-Hun Lee 4 Seong-Ho Koh 5
Affiliations

Affiliations

  • 1 Department of Neurology, Hanyang University College of Medicine, Guri, Gyeonggi, Korea.
  • 2 Department of Neuroscience, KAEL-Gemvax Co, Ltd, Seoul, Korea.
  • 3 Department of Translational Medicine, Hanyang University Graduate School of Biomedical Science & Engineering, Seoul, Korea.
  • 4 Department of Biochemistry and Molecular Biology, Hanyang University College of Medicine, Seoul, Korea.
  • 5 Department of Neurology, Hanyang University College of Medicine, Guri, Gyeonggi, Korea; Department of Translational Medicine, Hanyang University Graduate School of Biomedical Science & Engineering, Seoul, Korea. Electronic address: ksh213@hanyang.ac.kr.
Abstract

GV1001 is a 16-amino-acid vaccine peptide derived from the human telomerase Reverse Transcriptase sequence. We investigated the effects of GV1001 against β-amyloid (Aβ) oligomer-induced neurotoxicity in rat neural stem cells (NSCs). Primary culture NSCs were treated with several concentrations of GV1001 and/or Aβ₂₅₋₃₅ oligomer for 48 hours. GV1001 protected NSCs against the Aβ₂₅₋₃₅ oligomer in a concentration-dependent manner. Aβ₂₅₋₃₅ concentration dependently decreased viability, proliferation, and mobilization of NSCs and GV1001 treatment restored the cells to wild-type levels. Aβ₂₅₋₃₅ increased free radical levels in rat NSCs while combined treatment with GV1001 significantly reduced these levels. In addition, GV1001 treatment of Aβ₂₅₋₃₅-injured NSCs increased the expression level of survival-related proteins, including mitochondria-associated survival proteins, and decreased the levels of death and inflammation-related proteins, including mitochondria-associated death proteins. Together, these results suggest that GV1001 possesses neuroprotective effects against Aβ₂₅₋₃₅ oligomer in NSCs and that these effects are mediated through mimicking the extra-telomeric functions of human telomerase Reverse Transcriptase, including the induction of cellular proliferation, anti-apoptotic effects, mitochondrial stabilization, and Anti-aging and anti-oxidant effects.

Keywords

GV1001; Neural stem cells; Oligomer; Peptide; Vaccine; β-Amyloid.

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