Böttner Martina, Barrenschee Martina, Hellwig Ines, Harde Jonas, Egberts Jan-Hendrik, Becker Thomas, Zorenkov Dimitri, Schäfer Karl-Herbert, Wedel Thilo
Institute of Anatomy, Christian-Albrechts-University of Kiel, Kiel, Germany.
PLoS One. 2013 Jun 21;8(6):e66290. doi: 10.1371/journal.pone.0066290. Print 2013.
BACKGROUND & AIMS: Absence of glial cell line-derived neurotrophic factor (GDNF) leads to intestinal aganglionosis. We recently demonstrated that patients with diverticular disease (DD) exhibit hypoganglionosis suggesting neurotrophic factor deprivation. Thus, we screened mRNA expression pattern of the GDNF system in DD and examined the effects of GDNF on cultured enteric neurons.
Colonic specimens obtained from patients with DD (n = 21) and controls (n = 20) were assessed for mRNA expression levels of the GDNF system (GDNF, GDNF receptors GFRα1 and RET). To identify the tissue source of GDNF and its receptors, laser-microdissected (LMD) samples of human myenteric ganglia and intestinal muscle layers were analyzed separately by qPCR. Furthermore, the effects of GDNF treatment on cultured enteric neurons (receptor expression, neuronal differentiation and plasticity) were monitored.
mRNA expression of GDNF and its receptors was significantly down-regulated in the muscularis propria of patients with DD. LMD samples revealed high expression of GDNF in circular and longitudinal muscle layers, whereas GDNF receptors were also expressed in myenteric ganglia. GDNF treatment of cultured enteric neurons increased mRNA expression of its receptors and promoted neuronal differentiation and plasticity revealed by synaptophysin mRNA and protein expression.
Our results suggest that the GDNF system is compromised in DD. In vitro studies demonstrate that GDNF enhances expression of its receptors and promotes enteric neuronal differentiation and plasticity. Since patients with DD exhibit hypoganglionosis, we propose that the observed enteric neuronal loss in DD may be due to lacking neurotrophic support mediated by the GDNF system.
胶质细胞源性神经营养因子(GDNF)的缺失会导致肠道神经节缺如。我们最近发现,憩室病(DD)患者表现出神经节减少,提示存在神经营养因子缺乏。因此,我们筛选了DD中GDNF系统的mRNA表达模式,并研究了GDNF对培养的肠神经元的影响。
对21例DD患者和20例对照者的结肠标本进行评估,检测GDNF系统(GDNF、GDNF受体GFRα1和RET)的mRNA表达水平。为了确定GDNF及其受体的组织来源,通过定量PCR分别分析人肌间神经节和肠肌层的激光显微切割(LMD)样本。此外,监测GDNF处理对培养的肠神经元(受体表达、神经元分化和可塑性)的影响。
DD患者固有肌层中GDNF及其受体的mRNA表达显著下调。LMD样本显示,环行肌层和纵行肌层中GDNF高表达,而GDNF受体也在肌间神经节中表达。用GDNF处理培养的肠神经元可增加其受体的mRNA表达,并通过突触素mRNA和蛋白表达促进神经元分化和可塑性。
我们的结果表明,DD中GDNF系统受损。体外研究表明,GDNF可增强其受体的表达,并促进肠神经元分化和可塑性。由于DD患者表现出神经节减少,我们推测,DD中观察到的肠神经元丢失可能是由于缺乏GDNF系统介导的神经营养支持。