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Pluripotency of ES cells derived from tetraploid embryo complemented male mice


Abstract:
Pluripotent mouse embryonic stem (ES) cells have the ability to generate completely ES cell-derived mice by tetraploid (TE-4N) complementation although; derivation of ES cells from TE-4N animals has not been well defined. In this study, we generated TE-4N mice from high passage number ES cells and, in turn, determined the possibility of deriving ES cells from the TE-4N mice. The results showed that adult fertile TE-4N mice could be generated by aggregation of tetraploid embryos using ES cells passaged 23 times. Furthermore, ES cells could be derived from the TE-4N male mice and as judged by molecular characterisation and a study of chimeras, these ES cells were pluripotent. The findings demonstrate that tetraploid complementation is an efficient way to produce fertile mice, which can then give rise to pluripotent ES cells.

Keywords:
embryonic stem cells; pluripotency; tetraploid embryos


Autoři: Shuyu Li 1,2;  Baojiang Wu 2;  Hongyan Xue 2;  Lixia Zhao 2;  Jie Su 2;  Yunxia Li 1;  Wei Sun 2;  Shuxiang Hu 2;  Yao Li 1;  Siqin Bao 1;  Yanfeng Dai 1;  Jitong Guo 2;  Xihe Li 1,2*
Působiště autorů: Research Center for Animal Genetic Resources of Mongolia Plateau, College of Life Science, Inner Mongolia University, Hohhot, P. R. China 1;  Inner Mongolia Saikexing Reproductive Biotechnology Co. Ltd., Hohhot, P. R. China 2
Vyšlo v časopise: Cell Biology International Reports, 21, 2014, č. 2, s. 71-76
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1002/cbi3.10019

© 2014 The Authors. Cell Biology International Reports published by John Wiley & Sons Ltd on behalf of the International Federation for Cell Biology.
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Cell Biol Int Rep 21 (2014) 17–24  2014 The Authors. Cell Biology International Reports published by John Wiley & Sons Ltd on behalf of the International Federation for Cell Biology.© 2014 The Authors. Cell Biology International Reports published by John Wiley & Sons Ltd on behalf of the International Federation for Cell Biology.
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Cell Biol Int Rep 21 (2014) 17–24  2014 The Authors. Cell Biology International Reports published by John Wiley & Sons Ltd on behalf of the International Federation for Cell Biology.

Souhrn

Abstract:
Pluripotent mouse embryonic stem (ES) cells have the ability to generate completely ES cell-derived mice by tetraploid (TE-4N) complementation although; derivation of ES cells from TE-4N animals has not been well defined. In this study, we generated TE-4N mice from high passage number ES cells and, in turn, determined the possibility of deriving ES cells from the TE-4N mice. The results showed that adult fertile TE-4N mice could be generated by aggregation of tetraploid embryos using ES cells passaged 23 times. Furthermore, ES cells could be derived from the TE-4N male mice and as judged by molecular characterisation and a study of chimeras, these ES cells were pluripotent. The findings demonstrate that tetraploid complementation is an efficient way to produce fertile mice, which can then give rise to pluripotent ES cells.

Keywords:
embryonic stem cells; pluripotency; tetraploid embryos


Zdroje

1. Bao S, Tang F, Li X, Hayashi K, Gillich A, Lao K, Surani MA (2009) Epigenetic reversion of post-implantation epiblast to pluripotent embryonic stem cells. Nature 461: 1292–5.

2. Brook F, Gardner R (1997) The origin and efficient derivation of embryonic stem cells in the mouse. Proc Natl Acad Sci 94: 5709–12.

3. Bryja V, Bonilla S, Čajánek L, Parish CL, Schwartz CM, Luo Y, Rao MS, Arenas E (2006) An efficient method for the derivation of mouse embryonic stem cells. Stem Cells 24: 844–9.

4. Buehr M, Meek S, Blair K, Yang J, Ure J, Silva J, McLay R, Hall J, Ying Q-L, Smith A (2008) Capture of authentic embryonic stem cells from rat blastocysts. Cell 135: 1287–98.

5. Eggan K, Akutsu H, Loring J, Jackson-Grusby L, Klemm M, Rideout WM, Yanagimachi R, Jaenisch R (2001)Hybrid vigor, fetal overgrowth, and viability of mice derived by nuclear cloning and tetraploid embryo complementation. Proc Natl Acad Sci 98: 6209–14.

6. Eggan K, Jaenisch R (2003) Differentiation of F1 embryonic stem cells into viable male and female mice by tetraploid embryo complementation. Methods Enzymol 365: 25–39.

7. Evans MJ, Kaufman MH (1981) Establishment in culture of pluripotential cells from mouse embryos. Nature292: 154–6.

8. Kawase E, Suemori H, Takahashi N, Okazaki K, Hashimoto K, Nakatsuji N (1994) Strain difference in establishment of mouse embryonic stem (ES) cell lines. Int J Dev Biol 38: 385–90.

9. Kirchain SM, Hayward AM, Mkandawire JM, Qi P, Burds AA (2008) Comparison of tetraploid blastocyst microinjection of outbred Crl: CD1 (ICR), hybrid B6D2F1/Tac, and inbred C57BL/6NTac embryos for generation of mice derived from embryonic stem cells. Comp Med 58: 145–50.

10. Li X, Jia Q, Di K, Gao S, Wen X, Zhou R, Wei W, Wang LZ (2007) Passage number affects the pluripotency of mouse embryonic stem cells as judged by tetraploid embryo aggregation. Cell Tissue Res 327: 607–14.

11. Li X, Yu Y, Wei W, Yong J, Yang J, You J, Xiong X, Qing T, Deng H (2005) Simple and efficient production of mice derived from embryonic stem cells aggregated with tetraploid embryos. Mol Reprod Dev 71: 154–8.

12. McWhir J, Schnieke AE, Ansell R, Wallace H, Colman A, Scott AR, Kind AJ (1996) Selective ablation of differentiated cells permits isolation of embryonic stem cell lines from murine embryos with a non-permissive genetic background. Nat Genet 14: 223–6.

13. Nagy A, Gertsenstein M, Vintersten K, Behringer R (2003) Manipulating the mouse embryo: a laboratory manual. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.

14. Nagy A, Gocza E, Diaz EM, Prideaux V, Ivanyi E, Markkula M, Rossant J (1990) Embryonic stem cells alone are able to support fetal development in the mouse. Development 110: 815–21.

15. Nagy A, Rossant J, Nagy R, Abramow-Newerly W, Roder JC (1993) Derivation of completely cell culture-derived mice from early-passage embryonic stem cells. Proc Natl Acad Sci 90: 8424–8.

16. Wang Z-Q, Kiefer F, Urbánek P, Wagner EF (1997) Generation of completely embryonic stem cell-derived mutant mice using tetraploid blastocyst injection. Mech Dev 62: 137–45.

17. Ying Q-L, Wray J, Nichols J, Batlle-Morera L, Doble B, Woodgett J, Cohen P, Smith A (2008) The ground state of embryonic stem cell self-renewal. Nature 453: 519–23.

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