Znalesniak Eva B, Fu Ting, Guttek Karina, Händel Ulrike, Reinhold Dirk, Hoffmann Werner
Institute of Molecular Biology and Medicinal Chemistry, Otto-von-Guericke University Magdeburg, Germany.
Cell Physiol Biochem. 2016;39(6):2287-2296. doi: 10.1159/000447921. Epub 2016 Nov 7.
BACKGROUND/AIMS: The trefoil factor family (TFF) peptide TFF1 is a typical secretory product of the gastric mucosa and a very low level of expression occurs in nearly all regions of the murine brain. TFF1 possesses a lectin activity and binding to a plethora of transmembrane glycoproteins could explain the diverse biological effects of TFF1 (e.g., anti-apoptotic effect). It was the aim to test whether TFF expression is changed during neuroinflammation.
Expression profiling was performed using semi-quantitative RT-PCR analyses in two murine models of neuroinflammation, i.e. Toxoplasma gondii-induced encephalitis and experimental autoimmune encephalomyelitis (EAE), the latter being the most common animal model of multiple sclerosis. Tff1 expression was also localized using RNA in situ hybridization histochemistry.
We report for the first time on a significant transcriptional induction in cerebral Tff1 expression in both T. gondii-induced encephalitis and EAE. In contrast, Tff2 and Tff3 expression were not altered. Tff1 transcripts were predominantly localized in the internal granular layer of the cerebellum indicating neuronal expression. Furthermore, also glial cells are expected to express Tff1. Characterization of both experimental models by expression profiling (e.g., inflammasome sensors, inflammatory cytokines, microglial marker Iba1, ependymin related protein 1) revealed differences concerning the expression of the inflammasome sensor Nlrp1 and interleukin 17a.
The up-regulated expression of Tff1 is probably the result of a complex inflammatory process as its expression is induced by tumor necrosis factor α as well as interleukins 1β and 17. However on the transcript level, Tff1KO mice did not show any significant signs of an altered immune response after infection with T. gondii in comparison with the wild type animals.
背景/目的:三叶因子家族(TFF)肽TFF1是胃黏膜的典型分泌产物,在小鼠大脑几乎所有区域的表达水平都很低。TFF1具有凝集素活性,与大量跨膜糖蛋白结合可以解释TFF1的多种生物学效应(如抗凋亡效应)。本研究旨在检测神经炎症期间TFF表达是否发生变化。
在两种神经炎症小鼠模型中进行半定量逆转录-聚合酶链反应(RT-PCR)分析以进行表达谱分析,即弓形虫诱导的脑炎和实验性自身免疫性脑脊髓炎(EAE),后者是多发性硬化最常见的动物模型。还使用RNA原位杂交组织化学对Tff1表达进行定位。
我们首次报道在弓形虫诱导的脑炎和EAE中,大脑Tff1表达均有显著的转录诱导。相比之下,Tff2和Tff3表达未改变。Tff1转录本主要定位于小脑的内颗粒层,表明为神经元表达。此外,预计胶质细胞也表达Tff1。通过表达谱分析(如炎性小体传感器、炎性细胞因子、小胶质细胞标志物Iba1、ependymin相关蛋白1)对两种实验模型进行表征,揭示了炎性小体传感器Nlrp1和白细胞介素17a表达的差异。
Tff1表达上调可能是复杂炎症过程的结果,因为其表达受肿瘤坏死因子α以及白细胞介素1β和17诱导。然而在转录水平上,与野生型动物相比,Tff1基因敲除小鼠在感染弓形虫后未显示出免疫反应改变的任何显著迹象。