Lecoeur Constant, Swieb Salem, Zini Laurent, Rivière Charlotte, Combrisson Hélène, Ghérardi Romain, Abbou Claude, Yiou René
Service d'Urologie, Centre de Recherches Chirurgicales, Centre Hospitalier Universitaire Henri Mondor, France.
J Urol. 2007 Jul;178(1):332-7. doi: 10.1016/j.juro.2007.02.044. Epub 2007 May 15.
We investigated a new method of muscle precursor cell transfer in the urethra for the treatment of urinary incontinence, consisting of implanting myofibers with their satellite cells.
In preliminary experiments to test the regenerative capacities of satellite cells histological analysis was performed on days 7 and 30 after the implantation of myofiber cores in the urethra of 6 female pigs. In the main experiments 11 pigs underwent baseline urodynamics, followed by endoscopic destruction of the striated urethral sphincter located around the distal urethra (day 0). On day 30 circular myofiber strips in 7 experimental cases and adipocytes in 4 controls were implanted in the proximal urethra. Seven days later (day 37) 1 case was sacrificed to verify satellite cell activation. On day 60 urodynamics were performed without and with curarization. Urethral cryosections were immunostained for desmin (activated satellite cells), fast myosin heavy chain/bungarotoxin (myotubes/acetylcholine receptors), neurofilament/vesicular acetylcholine transporter (nerve endings) and CD45/CD68 (inflammatory response).
Preliminary histological studies revealed a myogenic process consisting of myofiber degeneration and satellite cell activation (day 7), followed by myotube formation replacing parental myofibers (day 30). In the main experiments endoscopic injury abolished striated urethral sphincter activity. Implantation of myofiber strips generated a pressure peak that decreased after curarization (mean+/-SEM 71.5+/-17.8 vs 33.5+/-14.8 cm H2O, p=0.031) and reappeared 60 minutes later, revealing that this action was tonic and under neural control. Nerve endings connected to the acetylcholine receptors of myotubes were observed on day 60. An inflammatory response was observed only on day 7 in the myofiber implantation group. Adipocyte implantation resulted in no significant intraurethral pressure changes.
Urethral implantation of myofibers regenerates as myotubes that exert tonic activity under neural control. This has potential clinical value as a means to create an additional striated urethral sphincter.
我们研究了一种将肌肉前体细胞移植到尿道治疗尿失禁的新方法,该方法包括植入带有卫星细胞的肌纤维。
在初步实验中,为测试卫星细胞的再生能力,在6只雌性猪的尿道植入肌纤维核心后的第7天和第30天进行了组织学分析。在主要实验中,11只猪接受了基线尿动力学检查,随后通过内镜破坏位于尿道远端周围的横纹尿道括约肌(第0天)。在第30天,7例实验病例植入环形肌纤维条,4例对照植入脂肪细胞于近端尿道。7天后(第37天)处死1例以验证卫星细胞激活。在第60天进行有无箭毒化的尿动力学检查。尿道冰冻切片进行结蛋白(活化卫星细胞)、快肌球蛋白重链/银环蛇毒素(肌管/乙酰胆碱受体)、神经丝/囊泡乙酰胆碱转运体(神经末梢)和CD45/CD68(炎症反应)免疫染色。
初步组织学研究显示,在第7天出现由肌纤维退变和卫星细胞激活组成的生肌过程,随后在第30天形成肌管替代亲代肌纤维。在主要实验中,内镜损伤消除了横纹尿道括约肌活动。植入肌纤维条产生一个压力峰值,箭毒化后降低(平均±标准误71.5±17.8对33.5±14.8 cm H2O,p = 0.031),60分钟后再次出现,表明该作用是紧张性的且受神经控制。在第60天观察到与肌管乙酰胆碱受体相连的神经末梢。仅在肌纤维植入组的第7天观察到炎症反应。脂肪细胞植入未导致尿道内压力有显著变化。
尿道植入肌纤维可再生为肌管,在神经控制下发挥紧张性活动。作为创建额外横纹尿道括约肌的一种手段,这具有潜在的临床价值。