Human Biology, Technische Universität München, Freising, Germany.
Gastroenterology. 2013 Apr;144(4):698-704.e4. doi: 10.1053/j.gastro.2013.01.040. Epub 2013 Jan 24.
Close association between nerves and mast cells in the gut wall provides the microanatomic basis for functional interactions between these elements, supporting the hypothesis that a mast cell-nerve axis influences gut functions in health and disease. Advanced morphology and imaging techniques are now available to assess structural and functional relationships of the mast cell-nerve axis in human gut tissues. Morphologic techniques including co-labeling of mast cells and nerves serve to evaluate changes in their densities and anatomic proximity. Calcium (Ca(++)) and potentiometric dye imaging provide novel insights into functions such as mast cell-nerve signaling in the human gut tissues. Such imaging promises to reveal new ionic or molecular targets to normalize nerve sensitization induced by mast cell hyperactivity or mast cell sensitization by neurogenic inflammatory pathways. These targets include proteinase-activated receptor (PAR) 1 or histamine receptors. In patients, optical imaging in the gut in vivo has the potential to identify neural structures and inflammation in vivo. The latter has some risks and potential of sampling error with a single biopsy. Techniques that image nerve fibers in the retina without the need for contrast agents (optical coherence tomography and full-field optical coherence microscopy) may be applied to study submucous neural plexus. Moreover, the combination of submucosal dissection, use of a fluorescent marker, and endoscopic confocal microscopy provides detailed imaging of myenteric neurons and smooth muscle cells in the muscularis propria. Studies of motility and functional gastrointestinal disorders would be feasible without the need for full-thickness biopsy.
肠壁中神经和肥大细胞的密切关联为这些元素之间的功能相互作用提供了微观解剖学基础,支持了肥大细胞-神经轴影响健康和疾病中肠道功能的假说。目前已有先进的形态学和成像技术可用于评估人类肠道组织中肥大细胞-神经轴的结构和功能关系。形态学技术,包括肥大细胞和神经的共标记,可用于评估它们的密度和解剖接近度的变化。钙(Ca(++))和电势染料成像为评估人类肠道组织中的肥大细胞-神经信号等功能提供了新的见解。这种成像有望揭示新的离子或分子靶点,以规范肥大细胞过度活跃或肥大细胞通过神经原性炎症途径致敏引起的神经敏化。这些靶点包括蛋白酶激活受体(PAR)1 或组胺受体。在患者中,体内肠道的光学成像有可能在体内识别神经结构和炎症。后者具有通过单次活检进行采样的风险和潜在的误差。不需要造影剂的用于成像视网膜神经纤维的技术(光学相干断层扫描和全场光学相干显微镜)可用于研究黏膜下神经丛。此外,黏膜下解剖、荧光标记的使用和内镜共聚焦显微镜可提供肌间神经和固有肌层平滑肌细胞的详细成像。无需全层活检即可进行运动和功能性胃肠道疾病的研究。