Deoxypodophyllotoxin, flavolignan, from Anthriscus sylvestris Hoffm. inhibits migration and MMP-9 via MAPK pathways in TNF-α-induced HASMC

Seok Jong Suh, Jeong Ran Kim, Un Ho Jin, Hong Seo Choi, Young Chae Chang, Young Choon Lee, Sung Hoon Kim, In Seon Lee, Tae Chul Moon, Hyeun Wook Chang, Cheorl Ho Kim

Research output: Contribution to journalArticlepeer-review

40 Scopus citations

Abstract

The matrix metalloproteinases (MMP-9 and MMP-2) in aortic smooth muscle cells (SMC) play key roles in the pathogenesis atherosclerosis. The SMC migration into the vascular wall via the bloodstream is directly linked with MMP-9 expression. Deoxypodophyllotoxin (DPT), a naturally occurring flavolignan with anti-inflammatory activity, was isolated from Anthriscus sylvestris Hoffm. and has been known inhibit the expression of MMP-9 in tumor necrosis factor-α (TNF-α) stimulated human aortic smooth muscle cells (HASMC). In this study, DPT was purified and demonstrated to inhibit the MMP-9/2 activities in TNF-α-induced HASMC. In addition, MMP-9 expression and migration was strongly inhibited by DPT in TNF-α-induced HASMC. To examine whether TNF-α-induced MMP-9 expressions are involved with migrations of HASMC, reverse transcription-polymerase chain reaction (RT-PCR) and luciferase-tagged promoter analysis were applied. These experiments revealed that DPT inhibited the mRNA transcription of MMP-9 gene expression. Furthermore, Western blot analysis indicated that the TNF-α-induced phosphorylation of extracellular signal regulated kinase 1 and 2 (ERK1/2), p38 and c-Jun N-terminal kinase (JNK) were strongly inhibited by DPT. From these results, it is concluded that DPT has an inhibitory activities on migration and MMP-2/9 activities, and MMP-9 transcription in HASMC.

Original languageEnglish
Pages (from-to)13-20
Number of pages8
JournalVascular Pharmacology
Volume51
Issue number1
DOIs
StatePublished - Jul 2009

Keywords

  • Deoxypodophyllotoxin
  • Extracellular matrix (ECM)
  • Human aortic smooth muscle cell
  • Matrix metalloproteinase-9/2
  • Mitogen-activated protein kinase
  • Tumor necrosis factor-α

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