Browse > Article
http://dx.doi.org/10.14348/molcells.2017.2223

Effects of Culture Dimensions on Maintenance of Porcine Inner Cell Mass-Derived Cell Self-Renewal  

Baek, Song (Department of Animal Life Science, Kangwon National University)
Han, Na Rae (Department of Animal Life Science, Kangwon National University)
Yun, Jung Im (Division of Animal Resource Science, Kangwon National University)
Hwang, Jae Yeon (Department of Cellular and Molecular Physiology, Yale School of Medicine)
Kim, Minseok (Animal Nutrition and Physiology Team, National Institute of Animal Science, RDA)
Park, Choon Keun (Department of Animal Life Science, Kangwon National University)
Lee, Eunsong (College of Veterinary Medicine, Kangwon National University)
Lee, Seung Tae (Department of Animal Life Science, Kangwon National University)
Abstract
Despite the fact that porcine embryonic stem cells (ESCs) are a practical study tool, in vitro long-term maintenance of these cells is difficult in a two-dimensional (2D) microenvironment using cellular niche or extracellular matrix proteins. However, a three-dimensional (3D) microenvironment, similar to that enclosing the inner cell mass of the blastocyst, may improve in vitro maintenance of self-renewal. Accordingly, as a first step toward constructing a 3D microenvironment optimized to maintain porcine ESC self-renewal, we investigated different culture dimensions for porcine ICM-derived cells to enhance the maintenance of self-renewal. Porcine ICM-derived cells were cultured in agarose-based 3D hydrogel with self-renewal-friendly mechanics and in 2D culture plates with or without feeder cells. Subsequently, the effects of the 3D microenvironment on maintenance of self-renewal were identified by analyzing colony formation and morphology, alkaline phosphatase (AP) activity, and transcriptional and translational regulation of self-renewal-related genes. The 3D microenvironment using a 1.5% (w/v) agarose-based 3D hydrogel resulted in significantly more colonies with stereoscopic morphology, significantly improved AP activity, and increased protein expression of self-renewal-related genes compared to those in the 2D microenvironment. These results demonstrate that self-renewal of porcine ICM-derived cells can be maintained more effectively in a 3D microenvironment than in a 2D microenvironment. These results will help develop novel culture systems for ICM-derived cells derived from diverse species, which will contribute to stimulating basic and applicable studies related to ESCs.
Keywords
agarose; culture dimension; embryonic stem cells; pig; self-renewal;
Citations & Related Records
Times Cited By KSCI : 1  (Citation Analysis)
연도 인용수 순위
1 Baker, B.M., and Chen, C.S. (2012). Deconstructing the third dimension: how 3D culture microenvironments alter cellular cues. J. Cell Sci. 125, 3015-3024.   DOI
2 Dixon, J.E., Shah, D.A., Rogers, C., Hall, S., Weston, N., Parmenter, C.D., McNally, D., Denning, C., and Shakesheff, K.M. (2014). Combined hydrogels that switch human pluripotent stem cells from selfrenewal to differentiation. Proc. Natl. Acad. Sci. USA 111, 5580-5585.   DOI
3 Donato, M.T., Castell, J.V., and Gomez-Lechon, M.J. (1999). Characterization of drug metabolizing activities in pig hepatocytes for use in bioartificial liver devices: comparison with other hepatic cellular models. J. Hepatol. 31, 542-549.   DOI
4 Gerecht, S., Burdick, J.A., Ferreira, L.S., Townsend, S.A., Langer, R., and Vunjak-Novakovic, G. (2007). Hyaluronic acid hydrogel for controlled self-renewal and differentiation of human embryonic stem cells. Proc. Natl. Acad. Sci. USA 104, 11298-11303.   DOI
5 Hughes, G.C., Post, M.J., Simons, M., and Annex, B.H. (2003). Translational physiology: porcine models of human coronary artery disease: implications for preclinical trials of therapeutic angiogenesis. J. Appl. Physiol. 94, 1689-1701.   DOI
6 Jang, M., Lee, S.T., Kim, J.W., Yang, J.H., Yoon, J.K., Park, J.C., Ryoo, H.M., van der Vlies, A.J., Ahn, J.Y., Hubbell, J.A., et al. (2013). A feeder-free, defined three-dimensional polyethylene glycol-based extracellular matrix niche for culture of human embryonic stem cells. Biomaterials 34, 3571-3580.   DOI
7 Lee, S.T., Yun, J.I., Jo, Y.S., Mochizuki, M., van der Vlies, A.J., Kontos, S., Ihm, J.E., Lim, J.M., and Hubbell, J.A. (2010). Engineering integrin signaling for promoting embryonic stem cell self-renewal in a precisely defined niche. Biomaterials 31, 1219-1226.   DOI
8 Lee, S.T., Yun, J.I., van der Vlies, A.J., Kontos, S., Jang, M., Gong, S.P., Kim, D.Y., Lim, J.M., and Hubbell, J.A. (2012). Long-term maintenance of mouse embryonic stem cell pluripotency by manipulating integrin signaling within 3D scaffolds without active Stat3. Biomaterials 33, 8934-8942.   DOI
9 Lunney. J.K. (2007). Advances in swine biomedical model genomics. Int. J. Biol. Sci. 3, 179-184.
10 Lou, Y.R., Kanninen, L., Kaehr, B., Townson, J.L., Niklander, J., Harjumaki, R., Jeffrey Brinker, C., and Yliperttula, M. (2015). Silica bioreplication preserves three-dimensional spheroid structures of human pluripotent stem cells and HepG2 cells. Sci. Rep. 5, 13635.   DOI
11 Meurens, F., Summerfield, A., Nauwynck, H., Saif, L., and Gerdts, V. (2012). The pig: a model for human infectious diseases. Trends Microbiol. 20, 50-57.   DOI
12 Musah S., Morin S.A., Wrighton P.J., Zwick, D.B., Jin, S., and Kiessling, L.L. (2012). Glycosaminoglycan-binding hydrogels enable mechanical control of human pluripotent stem cell self-renewal. ACS Nano 6, 10168-10177.   DOI
13 Pampaloni F., Reynaud E.G., and Stelzer E.H. (2007). The third dimension bridges the gap between cell culture and live tissue. Nat. Rev. Mol. Cell Biol. 8, 839-845.   DOI
14 Son, H.Y., Kim J.E., Lee, S.G., Kim, H.S., Lee, E., Park, J.K., Ka, H., Kim, H.J., and Lee, C.K. (2009). Efficient derivation and long term maintenance of pluripotent porcine embryonic stem-like cells. Asian-Aust J. Anim. Sci. 22, 26-34.   DOI
15 Ulrich T.A., Lee T.G., Shon H.K., Moon, D.W., and Kumar, S. (2011). Microscale mechanisms of agarose-induced disruption of collagen remodeling. Biomaterials 32, 5633-5642.   DOI
16 Valdes-Gonzalez, R.A., Dorantes, L.M., Garibay, G.N., Bracho-Blanchet, E., Mendez, A.J., Davila-Perez, R., Elliott, R.B., Teran, L., and White, D.J. (2005). Xenotransplantation of porcine neonatal islets of Langerhans and Sertoli cells: a 4-year study. Eur. J. Endocrinol. 153, 419-427.   DOI
17 Yuguo, L., and David, V.S. (2013). A fully defined and scalable 3D culture system for human pluripotent stem cell expansion and differentiation. Proc. Natl. Acad. Sci. USA 110, E5039-5048.   DOI
18 Van Cott, K.E., and Velander, W.H. (1998). Transgenic animals as drug factories: a new source of recombinant protein therapeutics. Exp. Opin. Investig. Drugs 7, 1683-1690.   DOI
19 Vassiliev, I., Vassilieva, S., Beebe, L.F., Harrison, S.J., McIlfatrick, S.M., and Nottle, M.B. (2010). In vitro and in vivo characterization of putative porcine embryonic stem cells. Cell Reprogram 12, 223-230.   DOI
20 Walters, E.M., Wolf, E., Whyte, J.J., Mao, J., Renner, S., Nagashima, H., Kobayashi, E., Zhao, J., Wells, K.D., Critser, J.K., et al. (2001). Completion of the swine genome will simplify the production of swine as a large animal biomedical model. BMC Med. Genomics 5, 55.