May Florian, Matiasek Kaspar, Vroemen Maurice, Caspers Christiane, Mrva Thomas, Arndt Christian, Schlenker Boris, Gais Peter, Brill Thomas, Buchner Alexander, Blesch Armin, Hartung Rudolf, Stief Christian, Gansbacher Bernd, Weidner Norbert
Department of Urology, Ludwig-Maximilians-Universität München, München, Germany.
Eur Urol. 2008 Nov;54(5):1179-87. doi: 10.1016/j.eururo.2008.02.003. Epub 2008 Feb 15.
Schwann cell-seeded guidance tubes have been shown to promote cavernous nerve regeneration, and the local delivery of neurotrophic factors may additionally enhance nerve regenerative capacity. The present study evaluates whether the transplantation of GDNF-overexpressing Schwann cells may enhance regeneration of bilaterally transected erectile nerves in rats.
Silicon tubes seeded with either GDNF-overexpressing or GFP-expressing Schwann cells were implanted into the gaps between transected cavernous nerve endings. Six (10 study nerves) or 12 wk (20 study nerves) postoperatively, erectile function was evaluated by relaparotomy, electrical nerve stimulation, and intracavernous pressure recording, followed by ultrastructural evaluation of reconstructed nerves employing bright-field and electron microscopy. Additional animals were either sham-operated (positive control; 20 study nerves) or received bilateral nerve transection without nerve reconstruction (negative control; 20 study nerves).
The combination of GDNF delivery and Schwann cell application promoted an intact erectile response in 90% (9 of 10) of grafted nerves after 6 wk and in 95% (19 of 20) after 12 wk, versus 50% (5 of 10) and 80% (16 of 20) of GFP-expressing Schwann cell grafts (p=0.02). The functional recovery was paralleled by enhanced axonal regeneration in GDNF-overexpressing Schwann cell grafts, as indicated by larger cross-sectional areas and a significantly higher percentage of neural tissue compared with GFP-transduced controls.
These findings demonstrate that the time required to elicit functional recovery of erectile nerves can be reduced by local delivery of GDNF. In terms of clinical application, this enhanced nerve repair might be critical for timely reinnervation of the corpus cavernosum as a prerequisite for functional recovery in men.
已证实接种雪旺细胞的引导管可促进海绵体神经再生,而局部递送神经营养因子可能会进一步增强神经再生能力。本研究评估过表达胶质细胞源性神经营养因子(GDNF)的雪旺细胞移植是否可增强大鼠双侧横断勃起神经的再生。
将接种过表达GDNF或绿色荧光蛋白(GFP)的雪旺细胞的硅胶管植入横断的海绵体神经末梢之间的间隙。术后6周(10条研究神经)或12周(20条研究神经),通过再次剖腹手术、电神经刺激和海绵体内压力记录评估勃起功能,随后采用明场和电子显微镜对重建神经进行超微结构评估。另外的动物进行假手术(阳性对照;20条研究神经)或接受双侧神经横断但不进行神经重建(阴性对照;20条研究神经)。
6周后,GDNF递送与雪旺细胞应用相结合使90%(10条中的9条)移植神经产生完整的勃起反应,12周后为95%(20条中的19条),而表达GFP的雪旺细胞移植分别为50%(10条中的5条)和80%(20条中的16条)(p=0.02)。与转导GFP的对照相比,过表达GDNF的雪旺细胞移植中轴突再生增强,功能恢复与之平行,表现为横截面积更大且神经组织百分比显著更高。
这些发现表明,通过局部递送GDNF可缩短勃起神经功能恢复所需的时间。就临床应用而言,这种增强的神经修复对于海绵体及时重新神经支配可能至关重要,这是男性功能恢复的前提条件。