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Advisor(s)
Abstract(s)
Cryopreservation of germ cells would
facilitate the availability of cells at any time allow ing the selection of donors and maintaining quality
control for further applications such as transplan tation and germline recovery. In the present study,
we analyzed the efciency of four cryopreservation
protocols applied either to isolated cell suspensions
or to testes fragments from Senegalese sole. In tes tes fragments, the quality of cryopreserved germ
cells was analyzed in vitro in terms of cell recovery,
integrity and viability, DNA integrity (fragmentation
and apoptosis), and lipid peroxidation (malondialde hyde levels). Transplantation of cryopreserved germ
cells was performed to check the capacity of cells to
in vivo incorporate into the gonadal primordium of
Senegalese sole early larval stages (6 days after hatch ing (dah), pelagic live), during metamorphosis (10
dah) and at post-metamorphic stages (16 dah and 20
dah, benthonic life). Protocols incorporating dimethyl
sulfoxide (DMSO) as a cryoprotectant showed higher
number of recovered spermatogonia, especially in
samples cryopreserved with L-15 + DMSO (0.39 ±
0.18 × 106
cells). Lipid peroxidation and DNA frag mentation were also signifcantly lower in this treat ment compared with other treatments. An important
increase in oxidation (MDA levels) was detected
in samples containing glycerol as a cryoprotectant,
refected also in terms of DNA damage. Transplan tation of L-15 + DMSO cryopreserved germ cells
into larvae during early metamorphosis (10 dah, 5.2
mm) showed higher incorporation of cells (27.30 ±
5.27%) than other larval stages (lower than 11%).
Cryopreservation of germ cells using testes fragments
frozen with L-15 + DMSO was demonstrated to be
a useful technique to store Senegalese sole germline.
Description
Keywords
Cryopreservation Spermatogonia Testicular germ cells Cell viability DNA fragmentation
Citation
Publisher
Springer