(-)-Epigallocatechin gallate but not chlorogenic acid suppresses EGF-stimulated migration of osteoblasts via attenuation of p38 MAPK activity

11Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.

Abstract

Phenolic compounds provide health benefits in humans. A previous study by our group has indicated that the epidermal growth factor (EGF)-induced migration of osteoblast-like MC3T3-E1 cells is mediated by the phosphorylation of p44/p42 mitogen-activated protein (MAPK), p38 MAPK, stress-activated protein kinase (SAPK)/c-Jun N-terminal kinase (JNK) and Akt, and that resveratrol, a major polyphenol in grape skin, suppresses the EGF-induced migration by attenuating Akt and SAPK/JNK activation. In the present study, the effects of chlorogenic acid, a major phenolic acid in coffee, and (-)-epigallocatechin gallate (EGCG), a major flavonoid in green tea, on the EGF-induced migration of MC3T3-E1 cells were investigated. EGCG significantly reduced the EGF-induced migration as evaluated by a Transwell migration assay and by a wound healing assay. However, chlorogenic acid failed to affect the EGF-induced migration. The phosphorylation of p38 MAPK induced by EGF was significantly suppressed by EGCG; however, the EGF-induced phosphorylation of p44/p42 MAP kinase, SAPK/JNK or Akt was not affected by EGCG. These results suggest that EGCG, but not chlorogenic acid, suppresses EGF-induced osteoblast migration through inhibiting p38 MAPK activation.

Cite

CITATION STYLE

APA

Kawabata, T., Otsuka, T., Fujita, K., Sakai, G., Matsushima-Nishiwaki, R., Kozawa, O., & Tokuda, H. (2018). (-)-Epigallocatechin gallate but not chlorogenic acid suppresses EGF-stimulated migration of osteoblasts via attenuation of p38 MAPK activity. International Journal of Molecular Medicine, 42(6), 3149–3156. https://doi.org/10.3892/ijmm.2018.3884

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free