
%0 Journal Article
%A Hao, Y. H. 
%A Wax, D. 
%A Zhong, Z. S. 
%A Murphy, C. N. 
%A Spate, L. 
%A Samuel, M. 
%A Rieke, A. 
%A Dyce, P. 
%A Li, J. L. 
%A Prather, R. S. 
%T 33 PRE-AND POST-IMPLANTATION DEVELOPMENT OF EMBRYOS CLONED FROM PORCINE SKIN-DERIVED SPHERE STEM CELLS
%J Reproduction, Fertility and Development
%D 2007/12/12
%V 20
%N 1
%P 97-97
%K 
%R https://doi.org/10.1071/RDV20N1AB33
%U https://www.publish.csiro.au/paper/RDV20N1AB33 
%X Although transgenic animals have been successfully cloned, the process is still inefficient. One of the limitations is the use of somatic donor cells that have a limited lifespan. If a genetic modification is made, the selection process must be initiated and completed rapidly or the cells will undergo senescence. Identification of a stem cell that would proliferate rapidly and not undergo senescence would prove to be very valuable. Here we report attempts at cloning by using porcine skin-derived sphere stem cells to determine if they are a suitable donor cell type. Skin-derived stem cells were isolated from fetal skin and express the neural progenitor marker NES, as well as genes that may be critical for pluripotency such as POU5F1 and STAT3. The skin-derived stem cells proliferate rapidly in vitro and retain a normal karyotype after long-term culture. In the present study, skin-derived stem cells were cultured and frozen in liquid nitrogen from passage 1 to passage 8. To investigate the developmental potential of the skin-derived stem cells, we performed nuclear transfer (NT) and compared their preimplantation developmental efficiency to that of the embryos derived from in vitro fertilization (IVF). Cumulus&#8211;oocyte complexes (COCs) were aspirated from antral follicles of ovaries from prepubertal gilts. Approximately, groups of 50-70 COCs were matured in vitro in 500 &#181;L TCM-199 per culture well for 40&#8211;44 h at 38.5°C, in a humidified atmosphere of 5% CO2 in air. The donor cells were thawed and cultured one day before NT; skin-derived stem cells were pipetted vigorously in PBS-EDTA to isolate individual cells. For IVF, cryopreserved ejaculated spermatozoa were thawed and washed and then resuspended with fertilization medium (mTBM). The MII oocytes were co-incubated with sperm for 6 h, and then transferred to PZM3 and cultured. For NT and IVF, respectively, the percent cleavage at 48 h in PZM3 was 64.9 ± 8.2% (169/208) and 62.1 ± 3.1% (94/184) (P > 0.05), the percent blastocysts after 6 days was 21.5 ± 5.8% (53/208) and 25.2 ± 3.4% (46/184) (P > 0.05), and the number of nuclei per blastocyst was 28.5 ± 1.9 (NT, maximum was 58) and 16.8 ± 4.0 (IVF, maximum was 31) (P < 0.05). To determine development post-implantation, some cloned embryos were cultured in PZM3 for 15.5 h and an average of 112 cloned embryos were transferred to the oviducts of four naturally cycling gilts on Day 0&#8211;1 of standing estrus. Three of the animals were pregnant: one of them farrowed two male piglets on August 14th, with the other two due on September 8th and 9th. Future studies will involve performing NT and ET on skin-derived stem cells from a higher passage number to determine if they would be suitable for genetic modification prior to NT. 
