May Florian, Buchner Alexander, Matiasek Kaspar, Schlenker Boris, Stief Christian, Weidner Norbert
Department of Urology, Ludwig Maximilians University, Munich 81377, Germany
Department of Urology, Ludwig Maximilians University, Munich 81377, Germany.
Dis Model Mech. 2016 Dec 1;9(12):1507-1511. doi: 10.1242/dmm.026518. Epub 2016 Nov 17.
Dissection of the cavernous nerves during radical prostatectomy for prostate cancer eliminates spontaneous erections. Using the rat as an experimental model, we compared the regenerative capacity of autologous nerve grafts and Schwann-cell-seeded nerve guides. After bilateral excision of cavernous nerve segments, cavernous nerves were reconstructed using unseeded silicon tubes, nerve autografts and silicon tubes seeded with either Glial-cell-line-derived (GDNF)-overexpressing or green fluorescent protein (GFP)-expressing Schwann cells (SCs) (16 study nerves per group). Control groups underwent either a sham operation or bilateral excision of cavernous nerve segments without repair. After 12 weeks erectile function was assessed by neurostimulation and intracavernous pressure (ICP) measurement. The reconstructed nerve segments were excised and histologically analyzed. We demonstrated an intact erectile response upon neurostimulation in 25% (4/16) of autologous nerve grafts, in 50% (8/16) of unseeded tubes, in 75% (12/16) of the Schwann-cell-GFP group and in 93.75% (15/16) of the GDNF group. ICP was significantly increased when comparing the Schwann-cell-GFP group with nerve autografts, unseeded conduits and negative controls (P<0.005). In conclusion, Schwann-cell-seeded scaffolds combined with neurotrophic factors are superior to unseeded tubes and autologous nerve grafts. They present a promising therapeutic approach for the repair of erectile nerve gaps.
在前列腺癌根治性前列腺切除术中,海绵体神经的离断会消除自然勃起功能。我们以大鼠作为实验模型,比较了自体神经移植和接种雪旺细胞的神经导管的再生能力。在双侧切除海绵体神经节段后,分别使用未接种的硅胶管、自体神经移植以及接种了过表达胶质细胞源性神经营养因子(GDNF)或绿色荧光蛋白(GFP)的雪旺细胞(SCs)的硅胶管对海绵体神经进行重建(每组16条实验神经)。对照组分别接受假手术或双侧切除海绵体神经节段但不进行修复。12周后,通过神经刺激和海绵体内压(ICP)测量评估勃起功能。切除重建的神经节段并进行组织学分析。我们发现,在接受神经刺激时,25%(4/16)的自体神经移植组、50%(8/16)的未接种硅胶管组、75%(12/16)的雪旺细胞-GFP组以及93.75%(15/16)的GDNF组出现了完整的勃起反应。将雪旺细胞-GFP组与自体神经移植组、未接种导管组和阴性对照组相比,ICP显著升高(P<0.005)。总之,接种雪旺细胞的支架结合神经营养因子优于未接种的导管和自体神经移植。它们为修复勃起神经间隙提供了一种有前景的治疗方法。