Le Duc Dung, Schmit David, Heck Sebastian, Omlor Albert Joachim, Sester Martina, Herr Christian, Schick Bernhard, Daubeuf François, Fähndrich Sebastian, Bals Robert, Frossard Nelly, Al Kadah Basel, Dinh Quoc Thai
Department of Experimental Pneumology and Allergology, Saarland University Hospital, Homburg, Germany.
Neuroimmunomodulation. 2016;23(5-6):261-270. doi: 10.1159/000453068. Epub 2016 Dec 29.
Mast cells (MCs) and nerves play an important role in allergic rhinitis (AR), but little is known about their crosstalk in AR. The aim of this study was to investigate MC-nerve interaction in the human nasal mucosa during AR.
The association between MCs and nerves, the expression of neuropeptide receptors (neurokinin 1 receptor [NK1R], neurokinin 2 receptor [NK2R], calcitonin gene-related peptide receptor [CGRPR], and MrgX2) on MCs, and protease-activated receptor 2 (PAR2) and tyrosine receptor kinase A (TrkA) on nerve fibres in the human nasal mucosa were investigated with immunofluorescence and real-time PCR.
The association between MCs and nerves was found to be significantly increased, although the numbers of MCs and nerve fibres were unchanged during AR. MCs expressing tryptase-chymase (MCtc) were frequently associated with nerve fibres and these contacts increased significantly in AR. Neuropeptide receptors NK1R, NK2R, and CGRPR were firstly found to be largely localised on MCs. The number of MCs expressing NK1R and NK2R, but not CGRPR, was significantly increased in AR. Interestingly, MCtc mostly expressed these neuropeptide receptors. The newly discovered tachykinin receptor MrgX2 was not expressed on nasal MCs, but was expressed on gland cells and increased in AR. Additionally, tachykinergic nerve fibres were found to express PAR2 or TrkA as receptors for MCs.
This study revealed for the first time an increase of MC-nerve association and neuropeptide receptor expression on MCs during AR as well as nerve fibres containing receptors for MCs. These results suggest that targeting or controlling airway sensory nerve function as a modulator of MCs may prevent allergic airway inflammation such as AR.
肥大细胞(MCs)和神经在变应性鼻炎(AR)中起重要作用,但它们在AR中的相互作用鲜为人知。本研究旨在探讨AR期间人鼻黏膜中MC与神经的相互作用。
采用免疫荧光和实时聚合酶链反应研究人鼻黏膜中MC与神经的关联、MC上神经肽受体(神经激肽1受体[NK1R]、神经激肽2受体[NK2R]、降钙素基因相关肽受体[CGRPR]和MrgX2)的表达,以及神经纤维上蛋白酶激活受体2(PAR2)和酪氨酸受体激酶A(TrkA)的表达。
虽然AR期间MC和神经纤维的数量没有变化,但发现MC与神经的关联显著增加。表达类胰蛋白酶-糜蛋白酶的MC(MCtc)经常与神经纤维相关联,并且这些接触在AR中显著增加。首次发现神经肽受体NK1R、NK2R和CGRPR主要定位于MC上。AR中表达NK1R和NK2R但不表达CGRPR的MC数量显著增加。有趣的是,MCtc大多表达这些神经肽受体。新发现的速激肽受体MrgX2在鼻MC上不表达,但在腺细胞上表达且在AR中增加。此外,发现速激肽能神经纤维表达PAR2或TrkA作为MC的受体。
本研究首次揭示了AR期间MC与神经的关联增加、MC上神经肽受体表达增加以及含有MC受体的神经纤维增加。这些结果表明,将气道感觉神经功能作为MC的调节剂进行靶向或控制可能预防AR等变应性气道炎症。