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Interleukin-18-mediated interferon-gamma secretion is regulated by thymosin beta 4 in human NK cells

Authors
Lee, Ha-reumYoon, Sun YoungSong, Seok BeanPark, YoorimKim, Tae SungKim, SeonghanHur, Dae YoungSong, Hyun KeunPark, HyunjeongCho, Daeho
Issue Date
Oct-2011
Publisher
ELSEVIER GMBH, URBAN & FISCHER VERLAG
Keywords
Interleukin-18; Natural killer cells; Thymosin beta 4; Interferon-gamma
Citation
IMMUNOBIOLOGY, v.216, no.10, pp 1155 - 1162
Pages
8
Journal Title
IMMUNOBIOLOGY
Volume
216
Number
10
Start Page
1155
End Page
1162
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/12481
DOI
10.1016/j.imbio.2011.04.002
ISSN
0171-2985
Abstract
Thymosin beta 4 (T beta 4) is the major G-actin sequestering molecule and is abundant in lymphoid tissues. However, it is not clear what regulates T beta 4 expression and what its function is on natural killer (NK) cells. We investigated whether interleukin-18 (IL-18) has a role in T beta 4 expression and if enhanced T beta 4 influences IL-18-mediated interferon-gamma (IFN-gamma) secretion. In this study, recombinant human IL-18 (rhIL-18) enhanced the endogenous level of T beta 4 through p38MAPK and JNK signaling pathway in the human NK cell line, NK-92MI. Overexpression of endogeneous T beta 4 stimulated IFN-gamma expression and secretion. Additionally, pretreatment with an inhibitor for T beta 4 decreased IL-18-enhanced IFN-gamma secretion, and transfection with T beta 4-specific short hairpin RNA resulted in reduction of IFN-gamma production in primary NK cells as well as in the human NK cell line. Taken together, these data indicated that T beta 4 is regulated by IL-18 and is involved in IL-18-enhanced IFN-gamma secretion in NK cells. (c) 2011 Elsevier GmbH. All rights reserved.
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