Author:
Wakayama Sayaka,Ito Daiyu,Ooga Masatoshi,Wakayama Teruhiko
Abstract
AbstractMouse cloning by nuclear transfer using freeze-drying (FD) somatic cells is now possible, but the success rate is significantly lower than that of FD spermatozoa. Because spermatozoa, unlike somatic cells, are haploid cells with hardened nuclei due to protamine, the factors responsible for their tolerance to FD treatment remain unclear. In this study, we attempt to produce offspring from FD spermatid, a haploid sperm progenitor cell whose nuclei, like somatic cells, have not yet been replaced by protamine. We developed a method for collecting FD spermatids from testicular suspension. Despite the significantly lower success rate than that of FD spermatozoa, healthy offspring were obtained when FD spermatids were injected into oocytes. Offspring were also obtained from FD spermatids derived from immature male mice that had not yet produced spermatozoa. These results suggest that nuclear protaminization, rather than haploid nuclei, is one of the key processes responsible for tolerance to FD treatment.
Funder
Takahashi Industrial and Economic Research Foundation
Naito Foundation
Japan Society for the Promotion of Science
Canon Foundation
Asada Science Foundation
Watanabe Fundation
Publisher
Springer Science and Business Media LLC
Cited by
1 articles.
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