| RRC ID |
43026
|
| 著者 |
Takano Y, Hiramatsu N, Okamura M, Hayakawa K, Shimada T, Kasai A, Yokouchi M, Shitamura A, Yao J, Paton AW, Paton JC, Kitamura M.
|
| タイトル |
Suppression of cytokine response by GATA inhibitor K-7174 via unfolded protein response.
|
| ジャーナル |
Biochem Biophys Res Commun
|
| Abstract |
K-7174, a GATA-specific inhibitor, is a putative anti-inflammatory agent that attenuates effects of inflammatory cytokines in certain cell types. However, molecular mechanisms involved have not been elucidated. We found that, in glomerular podocytes, induction of monocyte chemoattractant protein 1 (MCP-1) and inducible nitric oxide synthase (iNOS) by TNF-alpha was abrogated by K-7174. It was correlated with unexpected induction of unfolded protein response (UPR) evidenced by: (1) induction of endogenous indicators 78 kDa glucose-regulated protein and CCAAT/enhancer-binding protein-homologous protein, and (2) suppression of an exogenous indicator, endoplasmic reticulum stress-repressive alkaline phosphatase. In podocytes, induction of UPR by either tunicamycin, thapsigargin, A23187 or AB5 subtilase cytotoxin completely reproduced the suppressive effect of K-7174. Furthermore, K-7174-elicited UPR abrogated induction of MCP-1 and iNOS not only by TNF-alpha but also by medium conditioned by activated macrophages. These results suggested a novel, UPR-dependent mechanism underlying the anti-inflammatory potential of K-7174.
|
| 巻・号 |
360(2)
|
| ページ |
470-5
|
| 公開日 |
2007-8-24
|
| DOI |
10.1016/j.bbrc.2007.06.082
|
| PII |
S0006-291X(07)01325-3
|
| PMID |
17604001
|
| MeSH |
Animals
Anisoles / administration & dosage*
Azepines / administration & dosage*
Cell Line
Cytokines / metabolism*
Dose-Response Relationship, Drug
Endoplasmic Reticulum
GATA Transcription Factors / metabolism*
Mice
Podocytes / drug effects*
Podocytes / metabolism*
Protein Denaturation / drug effects
Protein Folding
|
| IF |
2.985
|
| 引用数 |
26
|
|
WOS 分野
|
BIOPHYSICS
BIOCHEMISTRY & MOLECULAR BIOLOGY
|
| リソース情報 |
| ヒト・動物細胞 |
|
