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脂多糖通过 NF-κB 和 p-c-Jun/c-Fos 的交联作用潜在地下调唾液腺 AQP5。

Potential down-regulation of salivary gland AQP5 by LPS via cross-coupling of NF-kappaB and p-c-Jun/c-Fos.

机构信息

Department of Molecular Oral Physiology, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima-shi, Tokushima, Japan.

出版信息

Am J Pathol. 2010 Aug;177(2):724-34. doi: 10.2353/ajpath.2010.090282. Epub 2010 Jun 3.

Abstract

The mRNA and protein levels of aquaporin (AQP)5 in the parotid gland were found to be potentially decreased by lipopolysaccharide (LPS) in vivo in C3H/HeN mice, but only weakly in C3H/HeJ, a TLR4 mutant mouse strain. In the LPS-injected mice, pilocarpine-stimulated saliva production was reduced by more than 50%. In a tissue culture system, the LPS-induced decrease in the AQP5 mRNA level was blocked completely by pyrrolidine dithiocarbamate, MG132, tyrphostin AG126, SP600125, and partially by SB203580, which are inhibitors for IkappaB kinase, 26S proteasome, ERK1/2, JNK, and p38 MAPK, respectively. In contrast, the expression of AQP1 mRNA was down-regulated by LPS and such down-regulation was blocked only by SP600125. The transcription factors NF-kappaB (p65 subunit), p-c-Jun, and c-Fos were increased by LPS given in vivo, whereas the protein-binding activities of the parotid gland extract toward the sequences for NF-kappaB but not AP-1-responsive elements present at the promoter region of the AQP5 gene were increased by LPS injection. Co-immunoprecipitation by using antibody columns suggested the physical association of the three transcription factors. These results suggest that LPS-induced potential down-regulation of expression of AQP5 mRNA in the parotid gland is mediated via a complex(es) of these two classes of transcription factors, NF-kappaB and p-c-Jun/c-Fos.

摘要

体内给予脂多糖(LPS)后,在 C3H/HeN 小鼠的腮腺中发现水通道蛋白(AQP)5 的 mRNA 和蛋白水平可能降低,但在 TLR4 突变鼠 C3H/HeJ 中仅轻微降低。在 LPS 注射的小鼠中,毛果芸香碱刺激的唾液分泌减少了 50%以上。在组织培养系统中,LPS 诱导的 AQP5 mRNA 水平降低被吡咯烷二硫代氨基甲酸盐、MG132、tyrphostin AG126、SP600125 和部分 SB203580 完全阻断,它们分别是 IkappaB 激酶、26S 蛋白酶体、ERK1/2、JNK 和 p38 MAPK 的抑制剂。相比之下,LPS 下调 AQP1 mRNA 的表达,这种下调仅被 SP600125 阻断。体内给予 LPS 后,转录因子 NF-kappaB(p65 亚基)、p-c-Jun 和 c-Fos 增加,而 LPS 注射后腮腺提取物对 AQP5 基因启动子区域 NF-kappaB 而不是 AP-1 反应元件的序列的蛋白结合活性增加。使用抗体柱的共免疫沉淀表明三种转录因子的物理关联。这些结果表明,LPS 诱导的腮腺中 AQP5 mRNA 表达的潜在下调是通过这两类转录因子 NF-kappaB 和 p-c-Jun/c-Fos 的复合物介导的。

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