Costunolide, a sesquiterpene lactone, inhibits the differentiation of pro-inflammatory CD4(+) T cells through the modulation of mitogen-activated protein kinases
- Authors
- Park, Eunchong; Song, Ju Han; Kim, Myun Soo; Park, Su-Ho; Kim, Tae Sung
- Issue Date
- 11월-2016
- Publisher
- ELSEVIER
- Keywords
- Costunolide; Anti-inflammation; T cell differentiation; ERK; p38
- Citation
- INTERNATIONAL IMMUNOPHARMACOLOGY, v.40, pp.508 - 516
- Indexed
- SCIE
SCOPUS
- Journal Title
- INTERNATIONAL IMMUNOPHARMACOLOGY
- Volume
- 40
- Start Page
- 508
- End Page
- 516
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/87068
- DOI
- 10.1016/j.intimp.2016.10.006
- ISSN
- 1567-5769
- Abstract
- CD4(+) T cell activation and adequate differentiation into effector T helper (Th) cells are crucial for mediating adaptive immune responses to cope with foreign pathogens. Despite the significant role of Th cells, excessive increases in their numbers result in inflammatory and autoimmune diseases. In this study, we investigated the effects of costunolide, a plant-derived natural compound with an anti-inflammatory activity, in regulating Th cells and the underlying mechanisms. Costunolide significantly decreased cell populations of differentiated Th1, Th2, and Th17 subsets under Th subset-polarizing conditions, while exerting statistically negligible effects on Treg cell differentiation. Furthermore, costunolide inhibited the expression level of Th subset-polarizing master genes such as T-bet, GATA3, and ROR-gamma t, indicating that costunolide inhibits the differentiation of CD4(+) T cells into Th subsets. Additionally, costunolide suppressed the proliferative activity of CD4(+) T cells and the expression of CD69 activation marker on CD4(+) T cells. When the molecular targets of costunolide were investigated, phosphorylation of ERK and p38 was found to be decreased under Th subset-polarizing conditions, whereas activity of JNK remained unchanged. U0126, an ERIC inhibitor, and SB203580, a p38 inhibitor, decreased the expression of CD69 upon TCR stimulation and inhibited CD4(+) T cell differentiation, indicating that both ERK and p38 are suggested to be critical molecular targets of costunolide. Taken together, these results suggest that costunolide inhibits the differentiation of CD4(+) T cells by suppressing ERIC and p38 activities and can be an effective therapeutic agent for T cell-mediated immune diseases. (C) 2016 Elsevier B.V. All rights reserved.
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Collections - Graduate School > Department of Life Sciences > 1. Journal Articles
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