4.7 Article

Neuroprotective effect of Cu,Zn-superoxide dismutase fused to a TCTP-derived protein transduction domain

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 666, Issue 1-3, Pages 87-92

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2011.05.040

Keywords

Kainic acid; Paraquat; Protein transduction domain; Superoxide dismutase; Translationally controlled tumor protein

Funding

  1. Ministry for Health, Welfare Family Affairs [A090030]
  2. Korean Government [2009-0064401]
  3. MEST [R01-2007-000-20263-0]
  4. Seoul RBD Program [ST090801]
  5. MOST/KOSEF [R15-2006-020]
  6. National Research Foundation of Korea [2009-0064401, R01-2007-000-20263-0] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Previously, we have reported that a 10-amino acid peptide (MIIYRDLISH) derived from the NH2-terminus of the human translationally controlled tumor protein (TCTP) functions as a protein transduction domain (PTD). In this study, we evaluated the transduction ability of SOD fused to TCTP-PTD (TCTP-SOD) into various cell lines. We also evaluated its ability to protect cells against paraquat-induced cell damage, in vitro and its neuroprotective effect in vivo against kainic acid-induced neuronal damage in an animal model. TCTP-SOD was transduced into various cell lines in a dose- and time-dependent manner without cytotoxic effect Furthermore, TCTP-SOD showed cytoprotective activity in SH-SY5Y cells, and intraperitoneally, injected TCTP-SOD was delivered into the mouse brain and protected the cells in the hippocampal region against the damage induced by kainic acid. We propose TCTP-SOD as a potential candidate drug for treatment of brain diseases. (C) 2011 Elsevier B.V. All rights reserved.

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