Planta Med 2011; 77(13): 1512-1518
DOI: 10.1055/s-0030-1270917
Biological and Pharmacological Activity
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Effects of Oxypeucedanin on Global Gene Expression and MAPK Signaling Pathway in Mouse Neuroblastoma Neuro-2A Cells

Joon-Seok Choi1 , Hyun-Young Shin1 , Ki-Sub Kwon1 , Seungwon Shin2 , Se-Young Choung3 , Yong-Soo Kwon 4 , Jae-Won Lee5 , Bong-Hwan Choi6 , Cheol-Koo Lee1
  • 1College of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea
  • 2College of Pharmacy, Duksung Women's University, Seoul, Republic of Korea
  • 3College of Pharmacy, KyungHee University, Seoul, Republic of Korea
  • 4College of Pharmacy, Kang Won National University, Chuncheon, Republic of Korea
  • 5Department of Statistics, College of Political Science and Economics, Korea University, Seoul, Republic of Korea
  • 6Division of Animal Genomics and Bioinformatics, National Institute of Animal Science, Rural Development Administration, Suwon, Republic of Korea
Weitere Informationen

Publikationsverlauf

received Dec. 28, 2010 revised February 13, 2011

accepted February 16, 2011

Publikationsdatum:
21. März 2011 (online)

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Abstract

Oxypeucedanin is a major coumarin aglycone that can be extracted from Ostericum koreanum. Coumarin aglycones have demonstrated various pharmacological effects, including anti-proliferation, anti-inflammation, and anti-pain. In this study, in order to understand the pharmacological properties of oxypeucedanin, we investigated global gene expression alteration in mouse neuroblastoma Neuro-2A cells. Results from the MTT assay indicated no decrease of cell viability up to 100 µM for 24 h. We measured gene expression profiles in Neuro-2A cells treated with either 10 µM or no oxypeucedanin for 24 h. We selected 128 differentially expressed genes (DEGs) for comparison of gene expression profiles by Bonferroni-adjusted p values (p < 0.1). Analysis of Gene Ontology (GO) biological process terms using the DEGs demonstrated the importance of protein metabolism, particularly ribosomal protein synthesis and protein degradation, intramembrane protein trafficking, and electron transport. Treatment with oxypeucedanin resulted in the downregulation of most DEGs for ribosomal protein synthesis and the electron transport chain (ETC). In contrast, most DEGs for protein degradation and cellular trafficking systems were upregulated. In addition, we found five upregulated DEGs for core and regulatory proteins involved in the mitogen-activated protein kinase (MAPK) signaling pathway. Independent translational validation of DEGs for MAPK signaling by immunoblot analysis showed consistent agreement with microarray data. Overall protein levels of Erk2 and p38MAPK were elevated, and their phosphorylated forms were also increased. These functional categories, based on transcriptional alteration and complicated modulation of MAPK signaling, might be underlying mechanisms responsible for the various pharmacological effects of oxypeucedanin.

References

Cheol-Koo Lee

318 West Building, College of Life Sciences and Biotechnology
Korea University

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