Muscle Precursor Cells for the Restoration of Irreversibly Damaged Sphincter Function

被引:56
作者
Eberli, Daniel
Aboushwareb, Tamer
Soker, Shay
Yoo, James J.
Atala, Anthony [1 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Wake Forest Inst Regenerat Med, Winston Salem, NC 27154 USA
基金
新加坡国家研究基金会;
关键词
Muscle precursor cells; Cellular therapy; Sphincter; Muscle regeneration; Incontinence; STRESS URINARY-INCONTINENCE; STRIATED URETHRAL SPHINCTER; STEM-CELLS; RISK-FACTORS; RAT MODEL; TISSUE; WOMEN; INJECTION; MYOBLASTS; TRANSPLANTATION;
D O I
10.3727/096368911X623835
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Multiple modalities, including injectable bulking agents and surgery, have been used to treat stress urinary incontinence. However, none of these methods is able to fully restore normal striated sphincter muscle function. In this study, we explored the possibility of achieving functional recovery of the urinary sphincter muscle using autologous muscle precursor cells (MPCs) as an injectable, cell-based therapy. A canine model of striated urinary sphincter insufficiency was created by microsurgically removing part of the sphincter muscle in 24 dogs. Autologous MPCs were obtained, expanded in culture, and injected into the damaged sphincter muscles of 12 animals. The animals were followed for up to 6 months after injection, and urodynamic studies, functional organ bath studies, ultrastructural and histological examinations were performed. Animals receiving MPC injections demonstrated sphincter pressures of approximately 80% of normal values, while the pressures in the control animals without cells dropped and remained at 20% of normal values. Histological analysis indicated that the implanted cells survived and formed tissue, including new innervated muscle fibers, within the injected region of the sphincter. These results indicate that autologous muscle precursor cells may be able to restore otherwise irreversibly damaged urinary sphincter function clinically.
引用
收藏
页码:2089 / 2098
页数:10
相关论文
共 38 条
[11]   Angiogenic gene-modified muscle cells for enhancement of tissue formation [J].
De Coppi, P ;
Delo, D ;
Farrugia, L ;
Udompanyanan, K ;
Yoo, JJ ;
Nomi, M ;
Atala, A ;
Soker, S .
TISSUE ENGINEERING, 2005, 11 (7-8) :1034-1044
[12]   Long-Term Contribution of Human Bone Marrow Mesenchymal Stromal Cells to Skeletal Muscle Regeneration in Mice [J].
de la Garza-Rodea, Anabel S. ;
van der Velde, Ietje ;
Boersma, Hester ;
Goncalves, Manuel A. F. V. ;
van Bekkum, Dirk W. ;
de Vries, Antoine A. F. ;
Knaan-Shanzer, Shoshan .
CELL TRANSPLANTATION, 2011, 20 (02) :217-231
[13]   Angiogenic gene modification of skeletal muscle cells to compensate for ageing-induced decline in bioengineered functional muscle tissue [J].
Delo, Dawn M. ;
Eberli, Daniel ;
Williams, J. Koudy ;
Andersson, Karl-Erik ;
Atala, Anthony ;
Soker, Shay .
BJU INTERNATIONAL, 2008, 102 (07) :878-884
[14]   Presentation and management of major complications of midurethral slings: Are complications under-reported? [J].
Deng, Donna Y. ;
Rutman, Matthew ;
Raz, Shlomo ;
Rodriguez, Larissa V. .
NEUROUROLOGY AND URODYNAMICS, 2007, 26 (01) :46-52
[15]   Optimization of human skeletal muscle precursor cell culture and myofiber formation in vitro [J].
Eberli, Daniel ;
Soker, Shay ;
Atala, Anthony ;
Yoo, James J. .
METHODS, 2009, 47 (02) :98-103
[16]   A canine model of irreversible urethral sphincter insufficiency [J].
Eberli, Daniel ;
Andersson, Karl-Erik ;
Yoo, James J. ;
Atala, Anthony .
BJU INTERNATIONAL, 2009, 103 (02) :248-253
[17]   Markers of collagen synthesis and degradation in urogenital tissue from women with and without stress urinary incontinence [J].
Edwall, L ;
Carlström, K ;
Jonasson, AF .
NEUROUROLOGY AND URODYNAMICS, 2005, 24 (04) :319-324
[18]   Purification and Characterization of Adipose-Derived Stem Cells From Patients With Lipoaspirate Transplant [J].
Folgiero, Valentina ;
Migliano, Emilia ;
Tedesco, Marinella ;
Iacovelli, Stefano ;
Bon, Giulia ;
Torre, Maria Luisa ;
Sacchi, Ada ;
Marazzi, Mario ;
Bucher, Stefania ;
Falcioni, Rita .
CELL TRANSPLANTATION, 2010, 19 (10) :1225-1235
[19]   Myoblasts Differentiated From Adipose-derived Stem Cells to Treat Stress Urinary Incontinence [J].
Fu, Qiang ;
Song, Xiao-Fei ;
Liao, Guo-Long ;
Deng, Chen-Liang ;
Cui, Lei .
UROLOGY, 2010, 75 (03) :718-723
[20]   Dystrophin expression in the mdx mouse restored by stem cell transplantation [J].
Gussoni, E ;
Soneoka, Y ;
Strickland, CD ;
Buzney, EA ;
Khan, MK ;
Flint, AF ;
Kunkel, LM ;
Mulligan, RC .
NATURE, 1999, 401 (6751) :390-394