Abstract
When sterile culture techniques of mammalian cells first became state of the art, there was tremendous anticipation that such cells could be eventually applied for therapeutic purposes. The discovery of adult human stem or progenitor cells further motivated scientists to pursue research in cell-based therapies. Although evidence from animal studies suggests that application of cells yields measurable benefits, in urology and many other disciplines, progenitor-cell-based therapies are not yet routinely clinically available. Stress urinary incontinence (SUI) is a condition affecting a large number of patients. The etiology of SUI includes, but is not limited to, degeneration of the urinary sphincter muscle tissue and loss of innervation, as well as anatomical and biomechanical causes. Therefore, different regimens were developed to treat SUI. However, at present, a curative functional treatment is not at hand. A progenitor-cell-based therapy that can tackle the etiology of incontinence, rather than the consequences, is a promising strategy. Therefore, several research teams have intensified their efforts to develop such a therapy for incontinence. Here, we introduce candidate stem and progenitor cells suitable for SUI treatment, show how the functional homogeneity and state of maturity of differentiated cells crucial for proper tissue integration can be assessed electrophysiologically prior to their clinical application, and discuss the trophic potential of adult mesenchymal stromal (or stem) cells in regeneration of neuronal function.
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Abbreviations
- ASC:
-
Adipose-derived stem cells (alias atMSC)
- bmMSC:
-
Bone marrow-derived MSC
- ESC:
-
Embryonic stem cell
- iPSC:
-
Induced pluripotent stem cells
- MC:
-
Muscle cell
- MEA:
-
Micro-electrode array
- MP:
-
Myogenic progenitor
- MSC:
-
Mesenchymal stromal cells, previously termed mesenchymal stem cells
- pMSC:
-
Term placenta-derived MSC
- ReST:
-
Regenerative Sphincter Therapy, an EU supported research network
- RiPSC:
-
RNA-mediated induced pluripotent stem cells
- SCI:
-
Spinal cord injury
- SMC:
-
Smooth muscle cell
- SUI:
-
Stress urinary incontinence
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Acknowledgments
We thank Tanja Abruzzese and Jan Maerz for their excellent technical help and Chaim Goziga for help in preparation of the artwork. Our own work briefly summarized in this review was in part supported by grants from the BMBF, DFG, fortüne, and Landesstiftung BW, and in part by institutional funding.
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Conflict of Interest
Dr. Melanie L. Hart reported no potential conflicts of interest relevant to this article.
Dr. Katharina M. H. Neumayer reported no potential conflicts of interest relevant to this article.
Dr. Martin Vaegler reported no potential conflicts of interest relevant to this article.
Dr. Lisa Daum reported no potential conflicts of interest relevant to this article.
Dr. Bastian Amend reported no potential conflicts of interest relevant to this article.
Dr. Karl D. Sievert reported no potential conflicts of interest relevant to this article.
Dr. Simone Di Giovanni reported no potential conflicts of interest relevant to this article.
Dr. Udo Kraushaar reported no potential conflicts of interest relevant to this article.
Dr. Elke Guenther reported no potential conflicts of interest relevant to this article.
Dr. Arnulf Stenzl serves as a Section Editor for Current Urology Reports.
Dr. Wilhelm K. Aicher reported no potential conflicts of interest relevant to this article.
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Hart, M.L., Neumayer, K.M.H., Vaegler, M. et al. Cell-Based Therapy for the Deficient Urinary Sphincter. Curr Urol Rep 14, 476–487 (2013). https://doi.org/10.1007/s11934-013-0352-7
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DOI: https://doi.org/10.1007/s11934-013-0352-7