State of the art of where we are at using stem cells for stress urinary incontinence

被引:32
作者
Furuta, Akira [1 ]
Jankowski, Ron J. [1 ]
Honda, Masashi [1 ]
Pruchnic, Ryan [1 ]
Yoshimura, Naoki [1 ]
Chancellor, Michael B. [1 ]
机构
[1] Univ Pittsburgh, Dept Urol, Sch Med, Pittsburgh, PA 15260 USA
关键词
adipose; muscle; nerve growth factor; stem cells; urinary incontinence; urethral sphincter;
D O I
10.1002/nau.20448
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Aims: This review aims to discuss: 1) the neurophysiology, highlighting the importance of the middle urethra, and treatment of stress urinary incontinence (SUI); 2) current injectable cell sources for minimally-invasive treatment; and 3) the potential of muscle-derived stem cells (MDSCs) for the delivery of neurotrophic factors. Methods: A PUB-MED search was conducted using combinations of heading terms: urinary incontinence, urethral sphincter, stem cells, muscle, adipose, neurctrophins. In addition, we will update the recent work from our laboratory. Results: In anatomical and functional studies of human and animal urethra, the middle urethra containing rhabdo sphincter, is critical for maintaining continence. Cell-based therapies are most often associated with the use of autologous multipotent stem cells, such as the bone marrow stromal cells. However, harvesting bone marrow stromal stem cells is difficult, painful, and may yield low numbers of stem cells upon processing. In contrast, alternative autologous adult stem cells such as MDSCs and adipose-derived stem cells can be easily obtained in large quantities and with minimal discomfort. Not all cellular therapies are the same, as demonstrated by the differences in safety and efficacy from muscle-sourced MDSCs versus myoblasts versus fibroblasts. Conclusions: Transplanted stem cells may have the ability to undergo self-renewal and multipotent differentiation, leading to sphincter regeneration. In addition, such cells may release, or be engineered to release, neurotrophins with subsequent paracrine recruitment of endogenous host cells to concomitantly promote a regenerative response of nerve- integrated muscle. The dawn of a new paradigm in the treatment of SUI may be near.
引用
收藏
页码:966 / 971
页数:6
相关论文
共 71 条
[1]   LONG-TERM FOLLOW-UP OF WOMEN TREATED WITH PERURETHRAL TEFLON INJECTIONS FOR STRESS-INCONTINENCE [J].
BECKINGHAM, IJ ;
WEMYSSHOLDEN, G ;
LAWRENCE, WT .
BRITISH JOURNAL OF UROLOGY, 1992, 69 (06) :580-583
[2]  
Bent AE, 2001, NEUROUROL URODYNAM, V20, P157, DOI 10.1002/1520-6777(2001)20:2<157::AID-NAU18>3.0.CO
[3]  
2-A
[4]  
BLAIVAS JG, 1987, J UROLOGY, V138, pS97
[5]   Epidemiology and natural history of pelvic floor dysfunction [J].
Bump, RC ;
Norton, PA .
OBSTETRICS AND GYNECOLOGY CLINICS OF NORTH AMERICA, 1998, 25 (04) :723-+
[6]   Improved sphincter contractility after allogenic muscle-derived progenitor cell injection into the denervated rat urethra [J].
Cannon, TW ;
Lee, JY ;
Somogyi, G ;
Pruchnic, R ;
Smith, CP ;
Huard, J ;
Chancellor, MB .
UROLOGY, 2003, 62 (05) :958-963
[7]   Single institution clinical trial of muscle-derived cell injection to treat stress urinary incontinence [J].
Carr, LK ;
Steele, D ;
Steele, S ;
Wagner, D ;
Pruchnic, R ;
Jankowski, RJ ;
Erickson, J ;
De Miguel, F ;
Yoshimura, N ;
Huard, J ;
Chancellor, MB .
JOURNAL OF UROLOGY, 2006, 175 (04) :414-414
[8]  
Chancellor MB, 2000, NEUROUROL URODYNAM, V19, P279, DOI 10.1002/(SICI)1520-6777(2000)19:3<279::AID-NAU9>3.0.CO
[9]  
2-M
[10]   Recent advances in the neurophysiology of stress urinary incontinence [J].
Chancellor, MB ;
Perkin, H ;
Yoshimura, N .
SCANDINAVIAN JOURNAL OF UROLOGY AND NEPHROLOGY, 2005, 39 (01) :21-24