Department of Surgery, University of California, San Diego School of Medicine, USA.
Am J Physiol Gastrointest Liver Physiol. 2010 Dec;299(6):G1308-18. doi: 10.1152/ajpgi.00156.2010. Epub 2010 Aug 12.
The enteric nervous system may have an important role in modulating gastrointestinal barrier response to disease through activation of enteric glia cells. In vitro studies have shown that enteric glia activation improves intestinal epithelial barrier function by altering the expression of tight junction proteins. We hypothesized that severe injury would increase expression of glial fibrillary acidic protein (GFAP), a marker of enteric glial activation. We also sought to define the effects of vagal nerve stimulation on enteric glia activation and intestinal barrier function using a model of systemic injury and local gut mucosal involvement. Mice with 30% total body surface area steam burn were used as model of severe injury. Vagal nerve stimulation was performed to assess the role of parasympathetic signaling on enteric glia activation. In vivo intestinal permeability was measured to assess barrier function. Intestine was collected to investigate changes in histology; GFAP expression was assessed by quantitative PCR, by confocal microscopy, and in GFAP-luciferase transgenic mice. Stimulation of the vagus nerve prevented injury-induced intestinal barrier injury. Intestinal GFAP expression increased at early time points following burn and returned to baseline by 24 h after injury. Vagal nerve stimulation prior to injury increased GFAP expression to a greater degree than burn alone. Gastrointestinal bioluminescence was imaged in GFAP-luciferase transgenic animals following either severe burn or vagal stimulation and confirmed the increased expression of intestinal GFAP. Injection of S-nitrosoglutathione, a signaling molecule released by activated enteric glia cells, following burn exerts protective effects similar to vagal nerve stimulation. Intestinal expression of GFAP increases following severe burn injury. Stimulation of the vagus nerve increases enteric glia activation, which is associated with improved intestinal barrier function. The vagus nerve may mediate the signaling that occurs from the central nervous system to the enteric nervous system following gastrointestinal injury.
肠神经系统可能通过激活肠胶质细胞在调节胃肠道屏障对疾病的反应方面发挥重要作用。体外研究表明,通过改变紧密连接蛋白的表达,肠胶质细胞的激活可以改善肠道上皮屏障功能。我们假设严重损伤会增加神经胶质纤维酸性蛋白(GFAP)的表达,这是肠胶质细胞激活的标志物。我们还试图通过全身损伤和局部肠道黏膜受累模型来定义迷走神经刺激对肠胶质细胞激活和肠道屏障功能的影响。用 30%全身表面积蒸汽烧伤的小鼠作为严重损伤的模型。进行迷走神经刺激以评估副交感神经信号对肠胶质细胞激活的作用。通过体内肠道通透性测量来评估屏障功能。收集肠道以研究组织学变化;通过定量 PCR、共聚焦显微镜和 GFAP-荧光素酶转基因小鼠评估 GFAP 表达。迷走神经刺激可防止损伤引起的肠道屏障损伤。烧伤后早期肠道 GFAP 表达增加,损伤后 24 小时恢复到基线。损伤前的迷走神经刺激比单纯烧伤更能增加 GFAP 表达。在严重烧伤或迷走神经刺激后,在 GFAP-荧光素酶转基因动物中进行胃肠道生物发光成像,并证实肠道 GFAP 的表达增加。烧伤后注射 S-亚硝基谷胱甘肽(一种由激活的肠胶质细胞释放的信号分子)可发挥类似于迷走神经刺激的保护作用。严重烧伤后,肠道 GFAP 的表达增加。迷走神经刺激增加肠胶质细胞的激活,从而改善肠道屏障功能。迷走神经可能介导胃肠道损伤后从中枢神经系统到肠神经系统的信号传递。