Porcine embryonic stem cells: a possible source for cell replacement therapy
- PMID: 18770051
- DOI: 10.1007/s12015-008-9040-2
Porcine embryonic stem cells: a possible source for cell replacement therapy
Abstract
The development of porcine embryonic stem cell lines (pESC) has received renewed interest given the advances being made in the production of immunocompatible transgenic pigs. However, difficulties are evident in the production of pESCs in-vitro. This may largely be attributable to differences in porcine pre-implantation development compared to the mouse and human. Expression of oct4, nanog and sox2 differs in the zona-enclosed porcine blastocyst compared to its mouse and human counterparts, which may suggest that other factors may be responsible for maintaining porcine pluripotency in the early blastocyst. In addition, the epiblast forms considerably later, at days 7 to 8 when the porcine blastocyst begins to hatch and is maintained for 4 days before completely differentiating. This review covers an outline of the known molecular profile during porcine pre-implantation development and provides a history in the development of putative pESCs to date. Greater knowledge on the molecular mechanisms that underlie porcine pluripotency and pre-implantation development may aid in improving the development of pESCs.
Similar articles
-
Apoptosis in Porcine Pluripotent Cells: From ICM to iPSCs.Int J Mol Sci. 2016 Sep 12;17(9):1533. doi: 10.3390/ijms17091533. Int J Mol Sci. 2016. PMID: 27626414 Free PMC article. Review.
-
Attempting to Convert Primed Porcine Embryonic Stem Cells into a Naive State Through the Overexpression of Reprogramming Factors.Cell Reprogram. 2018 Oct;20(5):289-300. doi: 10.1089/cell.2017.0071. Cell Reprogram. 2018. PMID: 30277824
-
Breaking down pluripotency in the porcine embryo reveals both a premature and reticent stem cell state in the inner cell mass and unique expression profiles of the naive and primed stem cell states.Stem Cells Dev. 2014 Sep 1;23(17):2030-45. doi: 10.1089/scd.2013.0502. Epub 2014 Jun 20. Stem Cells Dev. 2014. PMID: 24742229
-
Analysis of co-expression of OCT4, NANOG and SOX2 in pluripotent cells of the porcine embryo, in vivo and in vitro.Theriogenology. 2011 Feb;75(3):513-26. doi: 10.1016/j.theriogenology.2010.09.019. Epub 2010 Nov 12. Theriogenology. 2011. PMID: 21074831
-
From zygote to implantation: morphological and molecular dynamics during embryo development in the pig.Reprod Domest Anim. 2009 Sep;44 Suppl 3:39-49. doi: 10.1111/j.1439-0531.2009.01482.x. Reprod Domest Anim. 2009. PMID: 19660079 Review.
Cited by
-
Apoptosis in Porcine Pluripotent Cells: From ICM to iPSCs.Int J Mol Sci. 2016 Sep 12;17(9):1533. doi: 10.3390/ijms17091533. Int J Mol Sci. 2016. PMID: 27626414 Free PMC article. Review.
-
Porcine Pluripotent Stem Cells Derived from IVF Embryos Contribute to Chimeric Development In Vivo.PLoS One. 2016 Mar 18;11(3):e0151737. doi: 10.1371/journal.pone.0151737. eCollection 2016. PLoS One. 2016. PMID: 26991423 Free PMC article.
-
Interleukin-7 enhances in vitro development and blastocyst quality in porcine parthenogenetic embryos.Front Vet Sci. 2022 Dec 8;9:1052856. doi: 10.3389/fvets.2022.1052856. eCollection 2022. Front Vet Sci. 2022. PMID: 36570506 Free PMC article.
-
miRNAs promote generation of porcine-induced pluripotent stem cells.Mol Cell Biochem. 2014 Apr;389(1-2):209-18. doi: 10.1007/s11010-013-1942-x. Epub 2014 Jan 24. Mol Cell Biochem. 2014. PMID: 24464032
-
MicroRNAs: Important Regulators of Induced Pluripotent Stem Cell Generation and Differentiation.Stem Cell Rev Rep. 2018 Feb;14(1):71-81. doi: 10.1007/s12015-017-9785-6. Stem Cell Rev Rep. 2018. PMID: 29143183 Review.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials