Persistence and survival of autologous muscle derived cells versus bovine collagen as potential treatment of stress urinary incontinence

被引:79
作者
Yokoyama, T [1 ]
Yoshimura, N
Dhir, R
Qu, ZQ
Fraser, MO
Kumon, H
De Groat, WC
Huard, J
Chancellor, MB
机构
[1] Univ Pittsburgh, Sch Med, Dept Urol, Pittsburgh, PA 15261 USA
[2] Univ Pittsburgh, Sch Med, Dept Pharmacol, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Sch Med, Dept Orthoped Surg, Pittsburgh, PA 15261 USA
[4] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA 15261 USA
[5] Okayama Univ, Sch Med, Dept Urol, Okayama 700, Japan
关键词
urethra; collagen; urinary incontinence; stress; stem cells; transplantation; autologous;
D O I
10.1097/00005392-200101000-00077
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
Purpose: We explored the use of autologous muscle derived cells as a method of treating stress urinary incontinence. We determined whether urethral muscle derived cell injection is feasible and compared it with bovine collagen injection. Materials and Methods: Muscle derived cells isolated from female Sprague-Dawley rats were first transduced with retrovirus carrying the transgene for beta -galactosidase. We injected approximately 1 to 1.5 x 10(6) cells into the bladder wall and proximal urethra of 6 autologous animals. Tissue was harvested after 3 and 30 days, sectioned, stained for fast myosin heavy chain and assayed for beta -galactosidase. To compare muscle derived cell and bovine collagen injections 100 mul, of commercially available bovine collagen were also injected in Sprague-Dawley female rats. Tissue was harvested in 3 animals each after 3 and 30 days, sectioned and stained for trichrome. Subsequently, 3 adult SCID mice were used to compare the level of transgene expression at each time point after injecting 1.5 x 10(6) cells per injection, which were transduced with adenovirus carrying the transgene for beta -galactosidase. Results: A large number of cells expressing beta -galactosidase were observed in the bladder and urethral wall 3 and 30 days after autologous cell injection in Sprague-Dawley rats. The persistence of primary muscle derived cells at 3 days was similar to that of collagen. However, at 30 days there was significant cell persistence while only a minimal amount of injected bovine collagen was detectable. Approximately 88% of the beta -galactosidase expression at day 3 remained at day 30 in SCID mice. Conclusions: We present 2 new findings important for the emerging field of urological tissue engineering, including the feasibility of injecting autologous skeletal muscle derived cells into the lower urinary tract and the greater persistence of such injected cells versus injected bovine collagen. Therefore, autologous muscle derived cell injection may be an attractive alternative treatment option for stress urinary incontinence.
引用
收藏
页码:271 / 276
页数:6
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