An update of the interstitial cell compartment in the normal human bladder
Kamiel A J Kuijpers1, John P F A Heesakkers1, Theo G M Hafmans2
1Department of Urology, Radboud University Nijmegen Medical Centre, 267 Nijmegen, The Netherlands.
Insights
N-cadherin is a potential marker for identifying interstitial cells in the human bladder, which may be involved in overactive bladder conditions. This finding helps differentiate these crucial bladder cells.
Area of Science:
- Urology
- Cell Biology
- Histology
Background:
- Interstitial cells, or myofibroblasts, are implicated in overactive bladder pathogenesis.
- A specific phenotypic marker for these bladder interstitial cells is currently lacking.
Purpose of the Study:
- To investigate N-cadherin as a potential discriminatory marker for interstitial cells in the human bladder.
- To characterize N-cadherin expressing cells within bladder tissue.
Main Methods:
- Analysis of bladder biopsies (n=16) from patients undergoing cystectomy.
- Immunohistochemical staining for N-cadherin, PGP9.5, smoothelin, vimentin, and C-kit.
- Correlation of N-cadherin expression with bladder histology and myofibroblast ultrastructure.
Main Results:
- N-cadherin+/vimentin+ cells found in lamina propria and detrusor, associated with neurons.
- These N-cadherin+/vimentin+ cells resemble ultrastructurally defined myofibroblasts.
- A distinct population of N-cadherin+ cells co-localizing with C-kit was also identified.
Conclusions:
- N-cadherin serves as a discriminatory marker for interstitial cells in the human bladder.
- The bladder's interstitial compartment contains mesenchymal cells expressing N-cadherin, vimentin, and C-kit.
Aims:
Interstitial cells, also called myofibroblasts, most probably play a major role in the pathogenesis of the overactive bladder. However, no specific phenotypic marker has been identified. We investigated whether N-cadherin could play a role as a discriminatory marker for interstitial cells in the human bladder.
Methods:
Bladder biopsies (n = 16) were collected from macroscopically nonpathological locations during cystectomy which was performed because of bladder cancer. Tissue was analyzed for expression of N-cadherin. N-cadherin+ cells were phenotyped using antibodies against PGP9.5, smoothelin, vimentin, and C-kit. Findings were related to bladder tissue histology and ultrastructure of myofibroblastic cells.
Results:
N-cadherin+/vimentin+ cells with branched cell bodies were found in the lamina propria and detrusor layer. They were closely associated with neurons and showed no colocalization of PGP9.5 or smoothelin. A second type of N-cadherin+ cells was found at the boundary of detrusor bundles and in the lamina propria. These cells colocalization C-kit. We assumed that N-cadherin+/vimentin+ cells are similar to the ultrastructurally defined myofibroblasts.
Conclusions:
N-cadherin can play a role as a discriminatory marker for interstitial cells in the human bladder, as the interstitial compartment of the human bladder houses a population of cells from mesenchymal origin, immunopositive for N-cadherin, vimentin, and C-kit.
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