Mouse Round Spermatids Developed In Vitro from Preexisting Spermatocytes Can Produce Normal Offspring by Nuclear Injection into In Vivo-Developed Mature Oocytes
It has been shown that mature oocytes injected with nuclei from round spermatids collected from mouse testis can generate normal offspring and that round spermatids can develop in vitro. An undetermined issue is whether spermatids developed in vitro are capable of generating fertile offspring by nuc...
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Veröffentlicht in: | Biology of reproduction 2003-07, Vol.69 (1), p.169-176 |
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Zusammenfassung: | It has been shown that mature oocytes injected with nuclei from round spermatids collected from mouse testis can generate
normal offspring and that round spermatids can develop in vitro. An undetermined issue is whether spermatids developed in
vitro are capable of generating fertile offspring by nuclear injection into oocytes. Herein, we report the production of normal
and fertile offspring by nuclear injection using haploid spermatid donors derived from mouse primary spermatocyte precursors
cocultured with Sertoli cells. Cocultured spermatogonia and spermatocytes were characterized by their nuclear immunoreactive
patterns determined by an antibody to phosphorylated histone H2AX (γ-H2AX), a marker for DNA double-strand breaks. Cocultured
round spermatid progenies display more than one motile flagellum, whose axonemes were recognized by antitubulin immunostaining.
Flagellar wavelike movement and flagellar-driven propulsion of round spermatids developed in vitro were documented by videomicroscopy
(http://www.sci.ccny.cuny.edu/â¼kier). We also show that breeding of male and female mouse offspring generated by spermatid
nuclear injection produced fertile offspring. In addition to their capacity to produce fertile offspring, cocultured, flagellated
round spermatids can facilitate the analysis of the mechanisms of centriolar polarity, duplication, assembly, and flagellar
growth, including the intraflagellar transport of cargo proteins. |
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ISSN: | 0006-3363 1529-7268 |
DOI: | 10.1095/biolreprod.102.015099 |