Mukerji Gaurav, Yiangou Yiangos, Grogono Joanna, Underwood Jenny, Agarwal Sanjiv K, Khullar Vikram, Anand Praveen
Peripheral Neuropathy Unit, Hammersmith Hospital, Du Cane Road, London W12 0NN, UK.
J Urol. 2006 Jul;176(1):367-73. doi: 10.1016/S0022-5347(06)00563-5.
We studied the cellular localization of muscarinic receptor subtypes 2 and 3 in the human bladder and related any changes in overactive and painful bladder syndromes to measures of clinical dysfunction.
Bladder specimens obtained from patients with painful bladder syndrome (11), idiopathic detrusor overactivity (12) and from controls with asymptomatic microscopic hematuria (16) were immunostained using specific antibodies to muscarinic receptor subtypes 2 and 3, and to vimentin, which is a marker for myofibroblasts. Immunostaining results were quantified with computerized image analysis and correlated with clinical dysfunction using frequency and urgency scores.
Muscarinic receptor subtype 2 and 3 immunoreactivity was observed in the urothelium, nerve fibers and detrusor layers. In addition, strong myofibroblast-like cell staining, similar to vimentin, was present in the suburothelial region and detrusor muscle. A significant increase in suburothelial myofibroblast-like muscarinic receptor subtype 2 immunoreactivity was seen in patients with painful bladder syndrome (p = 0.0062) and idiopathic detrusor overactivity (p = 0.0002), and in muscarinic receptor subtype 3 immunoreactivity in those with idiopathic detrusor overactivity (p = 0.0122) with a trend in painful bladder syndrome. Muscarinic receptor subtype 2 and 3 immunoreactivity significantly correlated with the urgency score (p = 0.0002 and 0.0206, respectively) and muscarinic receptor subtype 2 immunoreactivity correlated with the frequency score (p = 0.0029). No significant difference was seen in urothelial and detrusor muscarinic receptor subtypes 2 and 3 or vimentin immunostaining.
To our knowledge this is the first study to show the cellular localization of muscarinic receptor subtypes 2 and 3 in the human bladder. The increase in muscarinic receptor subtypes 2 and 3 immunostaining in myofibroblast-like cells in clinical bladder syndromes and its correlation with clinical scores suggests a potential role in pathophysiological mechanisms and the therapeutic effect of anti-muscarinic agents.
我们研究了毒蕈碱受体2型和3型在人膀胱中的细胞定位,并将膀胱过度活动症和疼痛性膀胱综合征的任何变化与临床功能障碍指标相关联。
使用针对毒蕈碱受体2型和3型以及波形蛋白(一种肌成纤维细胞标志物)的特异性抗体,对从疼痛性膀胱综合征患者(11例)、特发性逼尿肌过度活动患者(12例)以及无症状显微镜下血尿对照者(16例)获取的膀胱标本进行免疫染色。免疫染色结果通过计算机图像分析进行定量,并使用频率和急迫性评分与临床功能障碍相关联。
在尿路上皮、神经纤维和逼尿肌层中观察到毒蕈碱受体2型和3型免疫反应性。此外,在尿路上皮下区域和逼尿肌中存在与波形蛋白相似的强肌成纤维细胞样细胞染色。在疼痛性膀胱综合征患者(p = 0.0062)和特发性逼尿肌过度活动患者(p = 0.0002)中,尿路上皮下肌成纤维细胞样毒蕈碱受体2型免疫反应性显著增加,在特发性逼尿肌过度活动患者中(p = 0.0122)毒蕈碱受体3型免疫反应性增加,在疼痛性膀胱综合征患者中有增加趋势。毒蕈碱受体2型和3型免疫反应性与急迫性评分显著相关(分别为p = 0.0002和0.0206),毒蕈碱受体2型免疫反应性与频率评分相关(p = 0.0029)。在尿路上皮和逼尿肌毒蕈碱受体2型和3型或波形蛋白免疫染色方面未观察到显著差异。
据我们所知,这是第一项显示毒蕈碱受体2型和3型在人膀胱中细胞定位的研究。临床膀胱综合征中肌成纤维细胞样细胞中毒蕈碱受体2型和3型免疫染色的增加及其与临床评分的相关性表明其在病理生理机制和抗毒蕈碱药物治疗效果中可能发挥作用。