Chen Jie, Rao Jaladanki N, Zou Tongtong, Liu Lan, Marasa Bernard S, Xiao Lan, Zeng Xing, Turner Douglas J, Wang Jian-Ying
Department of Surgery, Baltimore Veterans Affairs Medical Center, 10 North Greene Street, Baltimore, MD 21201, USA.
Am J Physiol Gastrointest Liver Physiol. 2007 Sep;293(3):G568-76. doi: 10.1152/ajpgi.00201.2007. Epub 2007 Jun 28.
The Toll-like receptors (TLRs) allow mammalian intestinal epithelium to detect various microbes and activate innate immunity after infection. TLR2 and TLR4 have been identified in intestinal epithelial cells (IECs) as fundamental components of the innate immune response to bacterial pathogens, but the exact mechanism involved in control of TLR expression remains unclear. Polyamines are implicated in a wide variety of biological functions, and regulation of cellular polyamines is a central convergence point for the multiple signaling pathways driving different epithelial cell functions. The current study determined whether polyamines regulate TLR expression, thereby modulating intestinal epithelial barrier function. Depletion of cellular polyamines by inhibiting ornithine decarboxylase (ODC) with alpha-difluoromethylornithine decreased levels of TLR2 mRNA and protein, whereas increased polyamines by ectopic overexpression of the ODC gene enhanced TLR2 expression. Neither intervention changed basal levels of TLR4. Exposure of normal IECs to low-dose (5 microg/ml) LPS increased ODC enzyme activity and stimulated expression of TLR2 but not TLR4, while polyamine depletion prevented this LPS-induced TLR2 expression. Decreased TLR2 in polyamine-deficient cells was associated with epithelial barrier dysfunction. In contrast, increased TLR2 by the low dose of LPS enhanced epithelial barrier function, which was abolished by inhibition of TLR2 expression with specific, small interfering RNA. These results indicate that polyamines are necessary for TLR2 expression and that polyamine-induced TLR2 activation plays an important role in regulating epithelial barrier function.
Toll样受体(TLRs)可使哺乳动物肠道上皮细胞在感染后检测各种微生物并激活先天免疫。TLR2和TLR4已在肠道上皮细胞(IECs)中被确定为对细菌病原体先天免疫反应的基本组成部分,但TLR表达调控的确切机制仍不清楚。多胺参与多种生物学功能,细胞内多胺的调控是驱动不同上皮细胞功能的多种信号通路的核心汇聚点。本研究确定多胺是否调节TLR表达,从而调节肠道上皮屏障功能。用α-二氟甲基鸟氨酸抑制鸟氨酸脱羧酶(ODC)来消耗细胞内多胺,可降低TLR2 mRNA和蛋白水平,而通过ODC基因异位过表达增加多胺则可增强TLR2表达。两种干预均未改变TLR4的基础水平。正常IECs暴露于低剂量(5μg/ml)脂多糖(LPS)会增加ODC酶活性并刺激TLR2表达,但不影响TLR4,而多胺消耗可阻止这种LPS诱导的TLR2表达。多胺缺乏细胞中TLR2减少与上皮屏障功能障碍有关。相反,低剂量LPS增加TLR2可增强上皮屏障功能,而用特异性小干扰RNA抑制TLR2表达可消除这种增强作用。这些结果表明多胺是TLR2表达所必需的,且多胺诱导的TLR2激活在调节上皮屏障功能中起重要作用。