Cynaropicrin, a sesquiterpene lactone, as a new strong regulator of CD29 and CD98 functions

Jae Youl Cho, Ae Ra Kim, Hong Gu Joo, Byung Hun Kim, Man Hee Rhee, Eun Sook Yoo, David R. Katz, Benjamin M. Chain, Jee H. Jung

Research output: Contribution to journalArticlepeer-review

41 Scopus citations

Abstract

Cynaropicrin is a sesquiterpene lactone displaying immunomodulatory effects on the production of cytokine and nitric oxide from macrophages/ monocytes. In this study we have examined inhibitory effect of cynaropicrin on activation of major adhesion molecules [CD29 (β1 integrins), CD43, and CD98] on the cells assessed by U937 (promonocytic cells) homotypic aggregation. Cynaropicrin potently blocked CD29 (β1 integrins)- and CD98-induced homotypic aggregation with IC50 values of 3.46 and 2.98 μM, respectively, without displaying cytotoxicity. Similarly, flow cytometric analysis exhibited that cynaropicrin down-regulated strikingly surface level of CD29 and CD147, a functional regulator of CD98, but not CD43. More importantly, cynaropicrin inhibition was linked to blockade of extracellular signal-related kinase (ERK) activation and distinct from other enzyme inhibitors including rottlerin, propranolol, forskolin, and chloroquine, but not cytochalasin B. Therefore, our finding is the first demonstration that cynaropicrin may be a potent functional regulator of CD29 and CD98 via interrupting ERK activation which may be linked to cytoskeleton rearrangement, suggesting further application to CD29- and CD98-mediated diseases such as virus-induced chronic inflammation, and invasion, migration, and metastasis of leukocyte cancer cells.

Original languageEnglish
Pages (from-to)954-961
Number of pages8
JournalBiochemical and Biophysical Research Communications
Volume313
Issue number4
DOIs
StatePublished - 23 Jan 2004

Keywords

  • Adhesion molecule
  • CD147
  • CD29 (β1 integrins)
  • CD98
  • Cynaropicrin
  • ERK
  • Homotypic aggregation
  • Sesquiterpene lactone

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