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The mouse small ubiquitin-like modifier-2 (SUMO-2) inhibits interleukin-12 (IL-12) production in mature dendritic cells by blocking the translocation of the p65 subunit of NF kappa B into the nucleus

Authors
Kim, Eun MiLee, Han-HyoungKim, Sang-HoonSon, Young-OkLee, Suk JunHan, JihyeBae, JoonbeomKim, Sang JoonPark, Chung-GyuPark, YongsooHwang, Kwang WooChun, Taehoon
Issue Date
9월-2011
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Dendritic cells; IL-12; NF kappa B; Post-translational modification; Sumoylation
Citation
MOLECULAR IMMUNOLOGY, v.48, no.15-16, pp.2189 - 2197
Indexed
SCIE
SCOPUS
Journal Title
MOLECULAR IMMUNOLOGY
Volume
48
Number
15-16
Start Page
2189
End Page
2197
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/111617
DOI
10.1016/j.molimm.2011.05.002
ISSN
0161-5890
Abstract
Post-translational modification by small ubiquitin-like modifier (SUMO) is involved in several significant cellular events. In particular, SUMO-1 and SUMO-4 modifications of I kappa B alpha have been shown to be actively involved in NF kappa B regulation. However, among the SUMO family, the specific function of SUMO-2/3 remains relatively unknown. In addition, it is not clear whether SUMO-2/3 follows the same functional role as SUMO-1 and SUMO-4 during the activation of NF kappa B. In this study, we examined the influence of mouse SUMO-2 during the maturation of dendritic cells (DCs). Our results showed that the ectopic expression of SUMO-2 does not affect the cell surface expression of MHC class II molecule (A(b)) and co-stimulatory molecules (CD80 and CD86), and the efficiency of antigen uptake. However, the ectopic expression of mouse SUMO-2 inhibited IL-12 secretion by blocking the translocation of the p65 subunit of NF kappa B into the nucleus, which led to the polarization of naive CD4(+) T cells to T helper 2 (Th2) shift in vitro. Further analyses showed that SUMO-2 directly modified I kappa B alpha. These results indicate that the functional role of SUMO-2/3 in the regulation of NF kappa B activity was conserved during evolution. (C) 2011 Elsevier Ltd. All rights reserved.
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