Division of Gastrointestinal Pathophysiology, Institute of Natural Medicine, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan.
Department of Pharmacology, School of Medicine, Batterjee Medical College for Sciences and Technology, Jeddah 21442, Saudi Arabia.
Cells. 2021 Jun 23;10(7):1586. doi: 10.3390/cells10071586.
Recently, the involvement of the nervous system in the pathology of allergic diseases has attracted increasing interest. However, the precise pathophysiological role of enteric neurons in food allergies has not been elucidated. We report the presence of functional high-affinity IgE receptors (FcεRIs) in enteric neurons. FcεRI immunoreactivities were observed in approximately 70% of cholinergic myenteric neurons from choline acetyltransferase-eGFP mice. Furthermore, stimulation by IgE-antigen elevated intracellular Ca concentration in isolated myenteric neurons from normal mice, suggesting that FcεRIs are capable of activating myenteric neurons. Additionally, the morphological investigation revealed that the majority of mucosal mast cells were in close proximity to enteric nerve fibers in the colonic mucosa of food allergy mice. Next, using a newly developed coculture system of isolated myenteric neurons and mucosal-type bone-marrow-derived mast cells (mBMMCs) with a calcium imaging system, we demonstrated that the stimulation of isolated myenteric neurons by veratridine caused the activation of mBMMCs, which was suppressed by the adenosine A3 receptor antagonist MRE 3008F20. Moreover, the expression of the adenosine A3 receptor gene was detected in mBMMCs. Therefore, in conclusion, it is suggested that, through interaction with mucosal mast cells, IgE-antigen-activated myenteric neurons play a pathological role in further exacerbating the pathology of food allergy.
最近,神经系统在过敏性疾病病理中的作用引起了越来越多的关注。然而,肠神经元在食物过敏中的精确病理生理作用尚未阐明。我们报告了功能性高亲和力 IgE 受体 (FcεRIs) 存在于肠神经元中。在胆碱乙酰转移酶-eGFP 小鼠的胆碱能肌间神经元中,约有 70%观察到 FcεRI 免疫反应性。此外,IgE-抗原刺激可使正常小鼠分离的肌间神经元内钙离子浓度升高,表明 FcεRIs 能够激活肌间神经元。此外,形态学研究表明,在食物过敏小鼠的结肠黏膜中,大多数黏膜肥大细胞与肠神经纤维接近。接下来,使用新开发的肌间神经元和黏膜型骨髓来源的肥大细胞 (mBMMCs) 的分离共培养系统和钙成像系统,我们证明了维拉帕米刺激分离的肌间神经元会导致 mBMMCs 的激活,而这种激活可被腺苷 A3 受体拮抗剂 MRE 3008F20 抑制。此外,在 mBMMCs 中检测到腺苷 A3 受体基因的表达。因此,综上所述,我们认为,通过与黏膜肥大细胞相互作用,IgE-抗原激活的肌间神经元在进一步加重食物过敏病理方面发挥了病理作用。