OBJECTIVE: We examined whether interstitial cells (ICs) of the human urinary bladder expressed β-adrenoceptor (AR) subtypes, and semiquantitatively compared the staining intensity among urothelium, ICs and detrusor muscles. METHODS: Paraffin sections of the human urinary bladder were obtained from histologically normal areas of formalin-fixed specimens removed for bladder carcinoma. Double-labeling immunohistochemical methods using antibodies against each β-AR subtype and vimentin were performed to identify ICs of the human urinary bladder. The staining intensity of β-ARs was semiquantitatively compared among urothelium, ICs and detrusor muscles. Further, gender-related difference or age-related correlation in the staining intensity of β-ARs was compared in the same cell types. RESULTS: The expression of β1 -, β2 -, and β3 -AR was observed in vimentin-positive ICs localized in suburothelium, between detrusor muscle bundles, and within these bundles of the human urinary bladder. The rank order of the staining intensity was urothelium > ICs = detrusor muscles in β1 -AR, urothelium > ICs > detrusor muscles in β2 -AR, whereas its order was ICs = detrusor muscles > urothelium in β3 -AR. Except for urothelial β1 -AR, there was no gender-related difference in the signal intensity of β-ARs in the urothelium, ICs or detrusor muscles. Age negatively correlated with the signal intensity of all β-AR subtypes. CONCLUSION: β-ARs were expressed in vimentin-positive ICs of the human urinary bladder. As for β2 - and β3 -AR, there was no gender-related difference or age-related correlation in urothelium, ICs and detrusor muscles. In the human urinary bladder, β-ARs expressed in ICs may play a role in bladder physiology.
OBJECTIVE: We examined whether interstitial cells (ICs) of the human urinary bladder expressed β-adrenoceptor (AR) subtypes, and semiquantitatively compared the staining intensity among urothelium, ICs and detrusor muscles. METHODS:Paraffin sections of the human urinary bladder were obtained from histologically normal areas of formalin-fixed specimens removed for bladder carcinoma. Double-labeling immunohistochemical methods using antibodies against each β-AR subtype and vimentin were performed to identify ICs of the human urinary bladder. The staining intensity of β-ARs was semiquantitatively compared among urothelium, ICs and detrusor muscles. Further, gender-related difference or age-related correlation in the staining intensity of β-ARs was compared in the same cell types. RESULTS: The expression of β1 -, β2 -, and β3 -AR was observed in vimentin-positive ICs localized in suburothelium, between detrusor muscle bundles, and within these bundles of the human urinary bladder. The rank order of the staining intensity was urothelium > ICs = detrusor muscles in β1 -AR, urothelium > ICs > detrusor muscles in β2 -AR, whereas its order was ICs = detrusor muscles > urothelium in β3 -AR. Except for urothelial β1 -AR, there was no gender-related difference in the signal intensity of β-ARs in the urothelium, ICs or detrusor muscles. Age negatively correlated with the signal intensity of all β-AR subtypes. CONCLUSION: β-ARs were expressed in vimentin-positive ICs of the human urinary bladder. As for β2 - and β3 -AR, there was no gender-related difference or age-related correlation in urothelium, ICs and detrusor muscles. In the human urinary bladder, β-ARs expressed in ICs may play a role in bladder physiology.