This protocol demonstrates methods for extracting sperm from the testes of males and then inseminating female mice. This procedure is useful when precise time is needed in developmental studies as well as transgenic work.
Abstract
Rodents of the genus Peromyscus (deer mice) are the most prevalent native North American mammals. Peromyscus species are used in a wide range of research including toxicology, epidemiology, ecology, behavioral, and genetic studies. Here they provide a useful model for demonstrations of artificial insemination.
Methods similar to those displayed here have previously been used in several deer mouse studies, yet no detailed protocol has been published. Here we demonstrate the basic method of artificial insemination. This method entails extracting the testes from the rodent, then isolating the sperm from the epididymis and vas deferens. The mature sperm, now in a milk mixture, are placed in the female’s reproductive tract at the time of ovulation. Fertilization is counted as day 0 for timing of embryo development. Embryos can then be retrieved at the desired time-point and manipulated.
Artificial insemination can be used in a variety of rodent species where exact embryo timing is crucial or hard to obtain. This technique is vital for species or strains (including most Peromyscus) which may not mate immediately and/or where mating is hard to assess. In addition, artificial insemination provides exact timing for embryo development either in mapping developmental progress and/or transgenic work. Reduced numbers of animals can be used since fertilization is guaranteed. This method has been vital to furthering the Peromyscus system, and will hopefully benefit others as well.
Protocol
Artificial Insemination Artificial insemination is used instead of natural matings to increase the chances that all the females have will become pregnant. 2 male was used for every 1 superovulated females or a female known to be in estrous. The caudae epididymides from mature male mice were placed in a 9% milk suspension and sliced open with 18 gauge needles. The sperm was allowed to swim freely for a few minutes and then the epididymides were taken from the mixture. The suspension was evaluated…
Acknowledgements
I would like to thank Mike Dewey from the Peromyscus Genetic Stock Center for his valuable insight, patience, and knowledge on rodent reproduction.