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Abstract
Testicular germ cell transplantation into the seminiferous
tubules is at present the only way to induce
spermatogenesis from a given source of spermatogonial stem
cells. Here we show an alternative method which harnesses
the self-organizing ability of testicular somatic cells.
The testicular cells of embryonic or neonatal mice or rats
and of newborn pigs were dissociated into single cells.
Each of them re-organized into a tubular structure
following implantation into the subcutis of
immunodeficient mice. When mouse germline stem (GS) cells,
derived from spermatogonial stem cells and expanded in
culture, were intermingled with testicular cells of
rodents, they were integrated in the reconstituted tubules
and differentiated beyond meiosis into spermatids. Normal
offspring were produced by the microinjection of those
spermatids into oocytes. This method could be applicable
to various mammalian species and useful for producing
functional gametes from GS cells in a xeno-ectopic
environment.
Key words:
Assisted Reproductive Technology
Testis
Gametogenesis
Meiosis
Spermatogenesis
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