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Neurotropic and neuroprotective activities of the earthworm peptide Lumbricusin.
Kim, Dae Hong; Lee, Ik Hwan; Nam, Seung Taek; Hong, Ji; Zhang, Peng; Hwang, Jae Sam; Seok, Heon; Choi, Hyemin; Lee, Dong Gun; Kim, Jae Il; Kim, Ho.
Afiliação
  • Kim DH; Department of Life Science, College of Natural Science, Daejin University, Pocheon, Gyeonggido 487-711, South Korea.
  • Lee IH; Department of Life Science, College of Natural Science, Daejin University, Pocheon, Gyeonggido 487-711, South Korea.
  • Nam ST; Department of Life Science, College of Natural Science, Daejin University, Pocheon, Gyeonggido 487-711, South Korea.
  • Hong J; Department of Life Science, College of Natural Science, Daejin University, Pocheon, Gyeonggido 487-711, South Korea.
  • Zhang P; Department of Life Science, College of Natural Science, Daejin University, Pocheon, Gyeonggido 487-711, South Korea.
  • Hwang JS; Department of Agricultural Biology, National Academy of Agricultural Science, RDA, Suwon 441-707, South Korea.
  • Seok H; Department of Biomedical Engineering, Jungwon University, Goesan, Chungcheongbukdo 367-700, South Korea.
  • Choi H; School of Life Sciences, KNU Creative Bioresearch Group (BK21 Plus Program), College of Natural Sciences, Kyungpook National University, Daehak-ro 80, Buk-gu, Daegu 702-701, South Korea.
  • Lee DG; School of Life Sciences, KNU Creative Bioresearch Group (BK21 Plus Program), College of Natural Sciences, Kyungpook National University, Daehak-ro 80, Buk-gu, Daegu 702-701, South Korea.
  • Kim JI; School of Life Sciences, Gwangju Institute of Science and Technology, Oryong-dong, Buk-gu, Gwangju 500-712, South Korea.
  • Kim H; Department of Life Science, College of Natural Science, Daejin University, Pocheon, Gyeonggido 487-711, South Korea. Electronic address: hokim@daejin.ac.kr.
Biochem Biophys Res Commun ; 448(3): 292-7, 2014 Jun 06.
Article em En | MEDLINE | ID: mdl-24796676
ABSTRACT
We recently isolated a polypeptide from the earthworm Lumbricus terrestris that is structurally similar to defensin, a well-known antibacterial peptide. An 11-mer antibacterial peptide (NH2-RNRRWCIDQQA), designated Lumbricusin, was synthesized based on the amino acid sequence of the isolated polypeptide. Since we previously reported that CopA3, a dung beetle peptide, enhanced neuronal cell proliferation, we here examined whether Lumbricusin exerted neurotropic and/or neuroprotective effects. Lumbricusin treatment induced a time-dependent increase (∼51%) in the proliferation of human neuroblastoma SH-SY5Y cells. Lumbricusin also significantly inhibited the apoptosis and decreased viability induced by treatment with 6-hydroxy dopamine, a Parkinson's disease-mimicking agent. Immunoblot analyses revealed that Lumbricusin treatment increased ubiquitination of p27(Kip1) protein, a negative regulator of cell-cycle progression, in SH-SY5Y cells, and markedly promoted its degradation. Notably, adenoviral-mediated over-expression of p27(Kip1) significantly blocked the antiapoptotic effect of Lumbricusin in 6-hydroxy dopamine-treated SH-SY5Y cells. These results suggest that promotion of p27(Kip1) degradation may be the main mechanism underlying the neuroprotective and neurotropic effects of Lumbricusin.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oligoquetos / Proteínas de Helminto / Fármacos Neuroprotetores / Peptídeos Catiônicos Antimicrobianos Limite: Animals / Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oligoquetos / Proteínas de Helminto / Fármacos Neuroprotetores / Peptídeos Catiônicos Antimicrobianos Limite: Animals / Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article