Novel Bioactive Peptides from Meretrix meretrix Protect Caenorhabditis elegans against Free Radical-Induced Oxidative Stress through the Stress Response Factor DAF-16/FOXO

Mar Drugs. 2018 Nov 11;16(11):444. doi: 10.3390/md16110444.

Abstract

The hard clam Meretrix meretrix, which has been traditionally used as medicine and seafood, was used in this study to isolate antioxidant peptides. First, a peptide-rich extract was tested for its protective effect against paraquat-induced oxidative stress using the nematode model Caenorhabditis elegans. Then, three novel antioxidant peptides; MmP4 (LSDRLEETGGASS), MmP11 (KEGCREPETEKGHR) and MmP19 (IVTNWDDMEK), were identified and were found to increase the resistance of nematodes against paraquat. Circular dichroism spectroscopy revealed that MmP4 was predominantly in beta-sheet conformation, while MmP11 and MmP19 were primarily in random coil conformation. Using transgenic nematode models, the peptides were shown to promote nuclear translocation of the DAF-16/FOXO transcription factor, a pivotal regulator of stress response and lifespan, and induce the expression of superoxide dismutase 3 (SOD-3), an antioxidant enzyme. Analysis of DAF-16 target genes by real-time PCR reveals that sod-3 was up-regulated by MmP4, MmP11 and MmP19 while ctl-1 and ctl-2 were also up-regulated by MmP4. Further examination of daf-16 using RNA interference suggests that the peptide-increased resistance of C. elegans to oxidative stress was DAF-16 dependent. Taken together, these data demonstrate the antioxidant activity of M. meretrix peptides, which are associated with activation of the stress response factor DAF-16 and regulation of the antioxidant enzyme genes.

Keywords: Caenorhabditis elegans; Meretrix meretrix; antioxidant peptides; oxidative stress; reactive oxygen species; transcription factor DAF-16/FOXO.

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Antioxidants / chemistry
  • Antioxidants / isolation & purification
  • Antioxidants / pharmacology*
  • Biological Assay / methods
  • Biological Factors / chemistry
  • Biological Factors / isolation & purification
  • Biological Factors / pharmacology*
  • Bivalvia / metabolism*
  • Caenorhabditis elegans / drug effects
  • Caenorhabditis elegans / physiology*
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / metabolism
  • Gene Expression Regulation / drug effects
  • Models, Animal
  • Oxidative Stress / drug effects*
  • Oxidative Stress / genetics
  • Paraquat / toxicity
  • Peptides / chemistry
  • Peptides / isolation & purification
  • Peptides / pharmacology
  • RNA Interference
  • Reactive Oxygen Species / metabolism

Substances

  • Antioxidants
  • Biological Factors
  • Caenorhabditis elegans Proteins
  • Forkhead Transcription Factors
  • Peptides
  • Reactive Oxygen Species
  • daf-16 protein, C elegans
  • Paraquat