A heptameric peptide isolated from the marine microalga Pavlova lutheri suppresses PMA-induced secretion of matrix metalloproteinase-9 through the inactivation of the JNK, p38, and NF-κB pathways in human fibrosarcoma cells

  • Seok Chun Ko
  • , Seong Yeong Heo
  • , Sung Wook Choi
  • , Zhong Ji Qian
  • , Soo Jin Heo
  • , Do Hyung Kang
  • , Namwon Kim
  • , Won Kyo Jung

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

In this study we isolate a heptameric peptide from the marine microalga Pavlova lutheri and examine its inhibitory effect and mechanism of action on the matrix metalloproteinase-9 (MMP-9) protein in human fibrosarcoma HT1080 cells. Through consecutive rounds of purification we isolated a potent MMP-9 inhibitory peptide composed of seven amino acids: Leu-Leu-Ala-Pro-Pro-Glu-Arg (796.4 Da). We show that the mRNA and protein expression levels of MMP-9 are reduced in the presence of this purified peptide. Furthermore, we show that this peptide inhibits PMA-induced translocation of nuclear factor-κB (NF-κB) by suppressing IκB-α phosphorylation and that it suppresses the phosphorylation of the c-Jun N-terminal (JNK) and p38 mitogen-activated protein kinases (MAPKs). Our results indicate that this peptide, purified from P. lutheri, has the potential to be a valuable natural preventive agent against MMP-related diseases.

Original languageEnglish
Pages (from-to)2367-2378
Number of pages12
JournalJournal of Applied Phycology
Volume30
Issue number4
DOIs
StatePublished - 1 Aug 2018

Bibliographical note

Publisher Copyright:
© 2018, Springer Science+Business Media B.V., part of Springer Nature.

Keywords

  • Marine microalga
  • Matrix metalloproteinase-9 (MMP-9)
  • Mitogen-activated protein kinases (MAPKs)
  • Nuclear factor-κB (NF-κB)
  • Pavlova lutheri

Fingerprint

Dive into the research topics of 'A heptameric peptide isolated from the marine microalga Pavlova lutheri suppresses PMA-induced secretion of matrix metalloproteinase-9 through the inactivation of the JNK, p38, and NF-κB pathways in human fibrosarcoma cells'. Together they form a unique fingerprint.

Cite this