In Vitro and In Vivo Development of Horse Cloned Embryos Generated with iPSCs, Mesenchymal Stromal Cells and Fetal or Adult Fibroblasts as Nuclear Donors

被引:25
|
作者
Olivera, Ramiro [1 ]
Natalia Moro, Lucia [2 ]
Jordan, Roberto [1 ]
Luzzani, Carlos [2 ]
Miriuka, Santiago [2 ]
Radrizzani, Martin [3 ]
Donadeu, F. Xavier [4 ,5 ,6 ]
Vichera, Gabriel [1 ]
机构
[1] KHEIRON SA Lab, Buenos Aires, DF, Argentina
[2] FLENI, Lab Biol Cell Dev, LIAN Unit, CONICET, Buenos Aires, DF, Argentina
[3] Natl Univ San Martin, CONICET, Lab Neruogenet & Mol Cytogent, Sch Sci, Buenos Aires, DF, Argentina
[4] Univ Edinburgh, Roslin Inst, Easter Bush, Midlothian, Scotland
[5] Univ Edinburgh, Royal Sch Vet Studies, Easter Bush, Midlothian, Scotland
[6] Univ Edinburgh, Euan MacDonald Ctr MND Res, Edinburgh, Midlothian, Scotland
来源
PLOS ONE | 2016年 / 11卷 / 10期
基金
英国生物技术与生命科学研究理事会;
关键词
PLURIPOTENT STEM-CELLS; UMBILICAL-CORD BLOOD; OSTEOGENIC CAPACITY; IMMATURE FOLLICLES; TIME-INTERVAL; SPERM EXTRACT; ACTIVATION; BOVINE; DIFFERENTIATION; OOCYTES;
D O I
10.1371/journal.pone.0164049
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The demand for equine cloning as a tool to preserve high genetic value is growing worldwide; however, nuclear transfer efficiency is still very low. To address this issue, we first evaluated the effects of time from cell fusion to activation (<1h, n = 1261; 1-2h, n = 1773; 2-3h, n = 1647) on in vitro and in vivo development of equine embryos generated by cloning. Then, we evaluated the effects of using different nuclear donor cell types in two successive experiments: I) induced pluripotent stem cells (iPSCs) vs. adult fibroblasts (AF) fused to ooplasts injected with the pluripotency-inducing genes OCT4, SOX2, MYC and KLF4, vs. AF alone as controls; II) umbilical cord-derived mesenchymal stromal cells (UC-MSCs) vs. fetal fibroblasts derived from an unborn cloned foetus (FF) vs. AF from the original individual. In the first experiment, both blastocyst production and pregnancy rates were higher in the 2-3h group (11.5% and 9.5%, respectively), respect to <1h (5.2% and 2%, respectively) and 1-2h (5.6% and 4.7%, respectively) groups (P<0.05). However, percentages of born foals/pregnancies were similar when intervals of 2-3h (35.2%) or 1-2h (35.7%) were used. In contrast to AF, the iPSCs did not generate any blastocyst-stage embryos. Moreover, injection of oocytes with the pluripotency-inducing genes did not improve blastocyst production nor pregnancy rates respect to AF controls. Finally, higher blastocyst production was obtained using UC-MSC (15.6%) than using FF (8.9%) or AF (9.3%), (P<0.05). Despite pregnancy rates were similar for these 3 groups (17.6%, 18.2% and 22%, respectively), viable foals (two) were obtained only by using FF. In summary, optimum blastocyst production rates can be obtained using a 2-3h interval between cell fusion and activation as well as using UC-MSCs as nuclear donors. Moreover, FF line can improve the efficiency of an inefficient AF line. Overall, 24 healthy foals were obtained from a total of 29 born foals.
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页数:14
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