Németh Zoltán H, Deitch Edwin A, Szabó Csaba, Fekete Zoltán, Hauser Carl J, Haskó György
Department of Surgery, UMD-New Jersey Medical School, Newark, New Jersey 07103, USA.
J Biol Chem. 2002 Mar 8;277(10):7713-9. doi: 10.1074/jbc.M109711200. Epub 2001 Dec 27.
Lithium has been documented to regulate apoptosis and apoptotic gene expression via NF-kappa B and mitogen-activated protein (MAP) kinase-dependent mechanisms. Since both NF-kappa B and MAP kinases are also important mediators of inflammatory gene expression, we investigated the effect of lithium on NF-kappa B- and MAP kinase-mediated inflammatory gene expression. Incubation of human intestinal epithelial cells with lithium induced both enhanced NF-kappa B DNA binding and NF-kappa B-dependent transcriptional activity. In addition, lithium stimulated activation of both the p38 and p42/44 MAP kinases. This lithium-induced up-regulation of NF-kappa B and MAP kinase activation was associated with an enhancement of interleukin-8 mRNA accumulation as well as an increase in interleukin-8 protein release. These proinflammatory effects of lithium were, in large part, mediated by activation of Na(+)/H(+) exchangers, because selective blockade of Na(+)/H(+) exchangers prevented the lithium-induced intestinal cell inflammatory response. These results demonstrate that lithium stimulates inflammatory gene expression via NF-kappa B and MAP kinase activation.
锂已被证明可通过核因子κB(NF-κB)和丝裂原活化蛋白(MAP)激酶依赖性机制调节细胞凋亡和凋亡基因表达。由于NF-κB和MAP激酶也是炎症基因表达的重要介质,我们研究了锂对NF-κB和MAP激酶介导的炎症基因表达的影响。用锂处理人肠上皮细胞可诱导NF-κB DNA结合增强和NF-κB依赖性转录活性增强。此外,锂刺激了p38和p42/44 MAP激酶的激活。锂诱导的NF-κB上调和MAP激酶激活与白细胞介素-8 mRNA积累增加以及白细胞介素-8蛋白释放增加有关。锂的这些促炎作用在很大程度上是由钠/氢交换体(Na(+)/H(+) exchangers)的激活介导的,因为选择性阻断Na(+)/H(+)交换体可防止锂诱导的肠细胞炎症反应。这些结果表明,锂通过激活NF-κB和MAP激酶来刺激炎症基因表达。