AB183. Clinical and cytogenetic characterization of a boy with a de novo pure partial trisomy 16q24.1-24.3 and complex chromosome rearrangement

Department of Urology, Renji Hospital, Shanghai Human Sperm Bank, Shanghai Jiao Tong University School of Medicine, Shanghai 200135, China; State Key Laboratory of Oncogenes and Related Genes, Stem Cell Research Center, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China; Shanghai Key Laboratory of Reproductive Medicine, Shanghai 200025, China; Shanghai Key Laboratory of Assisted Reproduction and Reproductive Genetics, Shanghai 200001, China Objective: Generation of functional spermatids from azoospermia patients is of unusual significance for treating male infertility. Here we report an efficient approach to obtain human functional spermatids from cryptorchid patients. Design: Comparative and controlled study. Materials and methods: Study was performed from January 2012 to May 2013 using Testicular biopsies obtained from cryptorchid patients and obstructive azoospermia patients from 25 to 37 years old. Multiplex PCR was carried to exclude Y chromosome microdeletion and male germ cells were obtained fromcryptorchid testes. Retinoic acid (RA) and stem cell factor (SCF) were used to induce differentiation of male germ cells enriched in spermatogonial stem cells from cryptorchid testes. Results: Spermatogonia remained whereas meiotic germ cells were rarein cryptorchid patients. Expression of numerous markers for meiotic and post-meiotic male germ cells was enhanced in human sermatogonial stem cells (SSCs) of cryptorchidism patients by RA and SCF treatment. Meiotic spreads and DNA content assays revealed that RA and SCF induced an obvious increase of SCP3-, MLH1and CREST-positive cells and haploid cells. Single-cell RNA sequencing analysis reflected distinct global gene profiles in the embryos derived from round spermatids and nucleus of somatic cells. Significantly, haploid spermatids generated from human SSCs of cryptorchid patients possessed fertilization and development capacity. Conclusions: This study thus provides an invaluable source of autologous male gametes for treating male infertility of azoospermia patients. Support: This study was supported by key grants from National Nature Science Foundation of China (31230048) and Chinese Ministry of Science and Technology (2013CB947901, 2010CB945200, 2014CB943101), grants from National Science Foundation of China (31201109 & 31171422), The Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning, Shanghai Pujiang Program (11PJ1406400), and a key grant from the Science and Technology Commission of Shanghai Municipality (12JC1405900).