The green tea catechin epigallocatechin gallate (EGCG) blocks cell motility, chemotaxis and development in Dictyostelium discoideum

PLoS One. 2013;8(3):e59275. doi: 10.1371/journal.pone.0059275. Epub 2013 Mar 14.

Abstract

Catechins, flavanols found at high levels in green tea, have received significant attention due to their potential health benefits related to cancer, autoimmunity and metabolic disease, but little is known about the mechanisms by which these compounds affect cellular behavior. Here, we assess whether the model organism Dictyostelium discoideum is a useful tool with which to characterize the effects of catechins. Epigallocatechin gallate (EGCG), the most abundant and potent catechin in green tea, has significant effects on the Dictyostelium life cycle. In the presence of EGCG aggregation is delayed, cells do not stream and development is typically stalled at the loose aggregate stage. The developmental effects very likely result from defects in motility, as EGCG reduces both random movement and chemotaxis of Dictyostelium amoebae. These results suggest that catechins and their derivatives may be useful tools with which to better understand cell motility and development in Dictyostelium and that this organism is a useful model to further characterize the activities of catechins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catechin / analogs & derivatives*
  • Catechin / pharmacology
  • Cell Movement / drug effects*
  • Chemotaxis / drug effects*
  • Cyclic AMP / metabolism
  • Dictyostelium / cytology*
  • Dictyostelium / drug effects*
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Catechin
  • epigallocatechin gallate
  • Cyclic AMP

Grants and funding

The work in the Sawai Lab was supported by JSPS Grant-in-Aid for Young Scientists (A) (22680024), Grant-in-Aid for Scientific Research on Innovative Areas (23111506), JST PRESTO program and in part by Human Frontier Science Program (RGY 70/2008) and Platform for Dynamic Approaches to Living Systems from MEXT, Japan. AN was supported by JSPS Grant-in-Aid for Research Activity Start-up (23870006). KJM was supported by the Colorado Mesa University (CMU) Biology Department and by Faculty Development Awards from CMU. ANI was supported by an undergraduate research award from Beta Beta Beta Honor Society. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.