Dorien Van Saen1, Ellen Goossens, Gert De Block, Herman Tournaye. 1. Center for Reproductive Medicine and Research Laboratories for Reproductive Medicine, University Hospital and Medical School, Dutch-Speaking Brussels Free University (Vrije Universiteit Brussel), Brussels, Belgium. dorien.van.saen@vub.ac.be
Abstract
OBJECTIVE: To make a comparison between two different approaches-spermatogonial stem cell transplantation and intratesticular grafting, for preservation and reintroduction of spermatogonial stem cells. DESIGN: Prospective experimental study. SETTING: Academic medical center and teaching hospital. PATIENT(S): N/A. INTERVENTION(S): Intratesticular transplantation, histologic evaluation of testes. MAIN OUTCOME MEASURE(S): Testicular weight, amount of green fluorescence in the testis, and immunostaining for green fluorescent protein. RESULT(S): In a first experiment donor-derived spermatogenesis was found in 65% of the injected testes (41.8 +/- 72.2 mm) compared with 75% of the testes (122.1 +/- 45.6 mm) after tissue grafting. In the second series of experiments complete spermatogenesis was found in 75% of the testes after fresh grafting (93.8 +/- 21.8 mm) compared with 88% after frozen-thawed tissue grafting (84.8 +/- 45.6 mm). CONCLUSION(S): Both approaches show that spermatogonial stem cells can successfully be introduced to the testis resulting in spermatogenesis. Tissue grafting produced a larger mean donor colony length and there was no significant difference between colonization efficiency using either fresh or frozen-thawed grafts. In a future clinical setting, grafting would be a simple and efficient way for reintroducing stem cells to the testis.
OBJECTIVE: To make a comparison between two different approaches-spermatogonial stem cell transplantation and intratesticular grafting, for preservation and reintroduction of spermatogonial stem cells. DESIGN: Prospective experimental study. SETTING: Academic medical center and teaching hospital. PATIENT(S): N/A. INTERVENTION(S): Intratesticular transplantation, histologic evaluation of testes. MAIN OUTCOME MEASURE(S): Testicular weight, amount of green fluorescence in the testis, and immunostaining for green fluorescent protein. RESULT(S): In a first experiment donor-derived spermatogenesis was found in 65% of the injected testes (41.8 +/- 72.2 mm) compared with 75% of the testes (122.1 +/- 45.6 mm) after tissue grafting. In the second series of experiments complete spermatogenesis was found in 75% of the testes after fresh grafting (93.8 +/- 21.8 mm) compared with 88% after frozen-thawed tissue grafting (84.8 +/- 45.6 mm). CONCLUSION(S): Both approaches show that spermatogonial stem cells can successfully be introduced to the testis resulting in spermatogenesis. Tissue grafting produced a larger mean donor colony length and there was no significant difference between colonization efficiency using either fresh or frozen-thawed grafts. In a future clinical setting, grafting would be a simple and efficient way for reintroducing stem cells to the testis.
Authors: Jonathan Poels; Gaël Abou-Ghannam; Sophie Herman; Anne Van Langendonckt; François-Xavier Wese; Christine Wyns Journal: Front Surg Date: 2014-12-02