首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Immunosuppressant FK506 induces interleukin-6 production through the activation of transcription factor nuclear factor (NF)-kappa(B). Implications for FK506 nephropathy.
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Immunosuppressant FK506 induces interleukin-6 production through the activation of transcription factor nuclear factor (NF)-kappa(B). Implications for FK506 nephropathy.

机译:免疫抑制剂FK506通过激活转录因子核因子(NF)-κB诱导白介素6的产生。对FK506肾病的影响。

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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-kappaB) critical for T cell activation. We show here that, contrary to the situation in T cells, FK506 activates transcription factor NF-kappaB in nonlymphoid cells such as fibroblasts and renal mesangial cells. We further show that FK506 induces NF-kappaB-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-kappaB activation/IL-6 production and some of FK506-induced renal abnormalities.
机译:FK506是目前使用的一种强大的免疫抑制药物,可抑制对T细胞活化至关重要的几种转录因子(核因子(NF)-AT和NF-kappaB)的活化。我们在这里表明,与T细胞中的情况相反,FK506激活非淋巴样细胞(如成纤维细胞和肾小球系膜细胞)中的转录因子NF-κB。我们进一步表明,FK506在体外和体内,特别是在肾脏中,诱导NF-κB调节的IL-6产生。先前已证明IL-6在体内会产生肾脏异常,例如血管增生性肾小球肾炎。在FK506治疗的动物中也观察到类似的肾脏异常。因此,这些结果表明,FK506诱导的NF-κB激活/ IL-6产生与FK506诱导的某些肾脏异常之间存在因果关系。

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