CXCL2型
泛素连接酶
基因敲除
泛素
化学
细胞生物学
MAP激酶激酶激酶
MAPK/ERK通路
下调和上调
炎症
趋化因子
激酶
分子生物学
癌症研究
生物
生物化学
免疫学
趋化因子受体
基因
细胞凋亡
作者
Xianwei Ma,Dan Wang,Na Li,Peng Gao,Mei Zhang,Yan Zhang
标识
DOI:10.1016/j.molimm.2018.10.005
摘要
NDR/LATS kinase family are conserved from yeast to man and their roles in inflammation remains largely unknown. In the present study, we show that knockdown of NDR2 significantly increases IL-17-induced IL-6, CXCL2 and CCL20 expression in Hela and HT-29 cells. Knockdown of NDR2 enhances IL-17-induced MAPK and NF-κB activation. NDR2 interacts with E3 ubiquitin protein ligase Smurf1, promotes Smurf1-mediated K48-linked ubiquitination of MEKK2 and inhibits expression of MEKK2. Consistently, knockdown of Smurf1 increases IL-17-induced IL-6, CXCL2 and CCL20 expression. On the other hand, overexpression of MEKK2 increases IL-17-induced IL-6 expression. These results suggest that NDR2 may play important roles in IL-17-associated inflammation by promoting Smurf1-mediated MEKK2 ubiquitination and degradation.
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