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Abstract
Spermatogonial stem cells (SSCs) continuously support
spermatogenesis after puberty. However, accumulating
evidence suggests that SSCs may functionally differ during
postnatal development. For example, mutant mice exist in
which SSCs support spermatogenesis in the first wave after
birth, but cease to do so thereafter, resulting in
infertility in adults. Studies using a retroviral vector
have shown that the vector transduces pup SSCs more
efficiently than adult SSCs, suggesting that pup SSCs
divide more frequently. Thus, it is hypothesized that SSCs
in pup and adult testes may have different
characteristics. As an approach to test this hypothesis,
in this study, we investigated the proliferation kinetics
of pup SSCs (6 - 9 days old) and their selfrenewal/
differentiation patterns during 2 months after
transplantation, and compared them to those of adult SSCs.
Using serial transplantation, we found that the number of
pup SSCs declined over the first week after
transplantation. Thereafter, it increased ~4-fold by 1 mo
and ~9-fold by 2 mo, indicating that pup SSCs continuously
proliferated from 1 wk to 2 mo after transplantation.
Compared to the proliferation of SSCs derived from adult
intact testes, that of pup SSCs was lower at 1 mo but
similar at 2 mo, indicating a delayed proliferation of pup
SSCs. However, pup SSCs regenerated spermatogenic colonies
of a similar length at 1 mo as SSCs from adult intact
testes. Therefore, these results suggest that some
functional differences exist in SSCs during postnatal
development, which may affect the potential of SSCs to
self-renew and differentiate.
Key words:
Testis
Developmental biology
Spermatogenesis
This article has been cited by other articles:
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J. R Yeh, X. Zhang, and M. C Nagano Establishment of a Short-Term In Vitro Assay for Mouse Spermatogonial Stem Cells Biol Reprod, November 1, 2007; 77(5): 897 - 904. [Abstract] [Full Text] [PDF] |
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