Helsel Aileen R, Oatley Jon M
Center for Reproductive Biology, School of Molecular Biosciences, College of Veterinary Medicine, Washington State University, Pullman, WA, USA.
Center for Reproductive Biology, College of Veterinary Medicine, Washington State University, 647521, Pullman, WA, 99164-7521, USA.
Methods Mol Biol. 2017;1463:155-172. doi: 10.1007/978-1-4939-4017-2_12.
In mammals, the activities of spermatogonial stem cells (SSCs) provide the foundation for continual spermatogenesis throughout a male's reproductive lifetime. At present, the defining characteristics of SSCs and mechanisms controlling their fate decisions are not well understood. Transplantation is a definitive functional measure of stem cell capacity for male germ cells that can be used as an assay to provide an unequivocal quantification of the SSC content in an experimental cell population. Here, we discuss the procedure for mice and provide protocols for preparing donor germ cell suspensions from testes directly or primary cultures of spermatogonia for transplantation, enriching for SSCs, preparing recipient males, microinjection into recipient testes, and considerations for experimental design.
在哺乳动物中,精原干细胞(SSCs)的活动为雄性整个生殖生命周期内持续的精子发生提供了基础。目前,SSCs的定义特征以及控制其命运决定的机制尚未完全明确。移植是对雄性生殖细胞干细胞能力的一种确定性功能检测,可作为一种测定方法,对实验细胞群体中的SSC含量进行明确量化。在此,我们讨论小鼠的操作流程,并提供相关方案,包括直接从睾丸制备供体生殖细胞悬液或用于移植的精原细胞原代培养物、富集SSCs、制备受体雄性小鼠、显微注射到受体睾丸以及实验设计的注意事项。