Testicular injection of busulfan for recipient preparation in transplantation of spermatogonial stem cells in mice
文献类型: 外文期刊
第一作者: Qin, Yusheng
作者: Qin, Yusheng;Liu, Ling;He, Yanan;Zhu, Huabin;Hao, Haisheng;Qin, Tong;Zhao, Xueming;Wang, Dong;Qin, Yusheng;Liang, Mingyuan;Ma, Wenzhi;Ma, Wenzhi
作者机构:
关键词: donor offspring;haematopoietic toxicity;intraperitoneal injections;vivo imaging
期刊名称:REPRODUCTION FERTILITY AND DEVELOPMENT ( 影响因子:2.311; 五年影响因子:2.396 )
ISSN: 1031-3613
年卷期: 2016 年 28 卷 12 期
页码:
收录情况: SCI
摘要: Intraperitoneal busulfan injections are used to prepare recipients for spermatogonial stem cell (SSC) transplantation but they are associated with haematopoietic toxicity. Testicular injections of busulfan have been proposed to overcome this limitation. To date, testicular injections have not been studied in the mouse model. Therefore, in the present study we used ICR mice as recipients for SSC transplantation and prepared these mice by testicular injection of busulfan on both sides (2, 3, 4 or 6mgkg(-1) per side). Following this, donor germ cells expressing red fluorescent protein (RFP) from transgenic C57BL/6J male mice were transplanted into recipients via the efferent duct on Days 16-17 after busulfan treatment. Positive control mice were prepared by intraperitoneal injection of 40mgkg(-1) busulfan and negative control mice were treated with bilateral testicular injection of 50% dimethyl sulfoxide. On Day 49 after transplantation, recipient mice that were RFP-positive by in vivo imaging were mated with ICR female mice. Donor-derived germ cell colonies with red fluorescence were observed on Day 60 after transplantation, and donor-derived offspring were obtained. The results demonstrated that endogenous germ cells were successfully eliminated in the seminiferous tubules via testicular busulfan administration, and that exogenous SSCs successfully undergo spermatogenesis in the testes of recipient mice prepared by testicular injections of busulfan. In addition to its effects on recipient preparation, this method was safe in rodents and could possibly be adapted for use in other species.
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