Dinh Q Thai, Groneberg David A, Peiser Christian, Mingomataj Ervin, Joachim Ricarda A, Witt Christian, Arck Petra C, Klapp Burghard F, Fischer Axel
Department of Medicine, Charité, School of Medicine, Humboldt University, Ostring 3, R. 3.0066, Augustenburger Platz 1, Berlin D-13353, Germany.
Respir Physiol Neurobiol. 2004 Nov 30;144(1):15-24. doi: 10.1016/j.resp.2004.08.001.
In the present study, the co-localisation of substance P (SP) with the vanilloid receptor TRPV1 and the neurotrophin receptor tyrosine kinase trkA was analysed in airway-specific murine dorsal root ganglion (DRG) neurons. DRG neurons labelled with Fast Blue were predominantly found at the segmental levels T2-T5. Immunoreactivity for the receptor TRPV1 was localized to 12% of Fast Blue labelled DRG neurons. Double-labelling immunohistochemistry revealed that a substantial number of them also co-express SP (7.6 +/- 1.1% (mean +/- S.E.M.)), whereas neurons with immunoreactivity for TRPV1 only were found in 4.4 +/- 1.3% of the retrogradely labelled neuronal population. Further analysis of retrogradely labelled neurons showed that their majority expressed trkA (62.8 +/- 1.4%), neurofilament protein 68-kDa (64.8 +/- 1.5%) or glutamate alone (19.5 +/- 1.9%). SP was always expressed in trkA-positive neurons. Based on the extent of co-localization of SP with the receptors TRPV1 and trkA in DRG airway neurons, the present study indicates that the DRG pathway may have effects on the magnitude of neurogenic inflammation in airway diseases such as asthma.
在本研究中,对气道特异性小鼠背根神经节(DRG)神经元中P物质(SP)与香草酸受体TRPV1和神经营养因子受体酪氨酸激酶trkA的共定位进行了分析。用快蓝标记的DRG神经元主要见于T2 - T5节段水平。TRPV1受体的免疫反应性定位于12%的快蓝标记的DRG神经元。双重免疫组织化学染色显示,其中大量神经元也共表达SP(7.6±1.1%(平均值±标准误)),而仅对TRPV1有免疫反应性的神经元在逆行标记的神经元群体中占4.4±1.3%。对逆行标记神经元的进一步分析表明,它们大多数表达trkA(62.8±1.4%)、68-kDa神经丝蛋白(64.8±1.5%)或仅表达谷氨酸(19.5±1.9%)。SP总是在trkA阳性神经元中表达。基于DRG气道神经元中SP与TRPV1和trkA受体的共定位程度,本研究表明DRG通路可能对哮喘等气道疾病中神经源性炎症的程度有影响。