Immunosuppressant FK506 induces interleukin-6 production through the activation of transcription factor nuclear factor (NF)-kappa B - Implications for FK506 nephropathy

被引:62
作者
Muraoka, K
Fujimoto, K
Sun, XG
Yoshioka, K
Shimizu, K
Yagi, M
Bose, H
Miyazaki, I
Yamamoto, K
机构
[1] KANAZAWA UNIV,CANC RES INST,DEPT MOLEC PATHOL,KANAZAWA,ISHIKAWA 920,JAPAN
[2] KANAZAWA UNIV,SCH MED,DEPT SURG 2,KANAZAWA,ISHIKAWA 920,JAPAN
[3] UNIV TEXAS,INST MOLEC & CELLULAR BIOL,AUSTIN,TX 78712
关键词
immunosuppressant; FK506; NF-kappa B; IL-6; nephrotoxicity;
D O I
10.1172/JCI118690
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
FK506 is a powerful immunosuppressive drug currently in use that inhibits the activation of several transcription factors (nuclear factor (NF)-AT and NF-kappa B) critical for T cell activation. We show here that, contrary to the situation in T cells, FK506 activates transcription factor NF-kappa B in non-lymphoid cells such as fibroblasts and renal mesangial cells. We further show that FK506 induces NF-kappa B-regulated IL-6 production in vitro and in vivo, in particular in kidney. IL-6 has been shown previously to produce renal abnormalities in vivo, such as mesangioproliferative glomerulonephritis. Similar renal abnormalities were also observed in FK506-treated animals. These results thus suggest a causal relationship between FK506-induced NF-kappa B activation/IL-6 production and some of FK506-induced renal abnormalities.
引用
收藏
页码:2433 / 2439
页数:7
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