Hostname: page-component-586b7cd67f-t8hqh Total loading time: 0 Render date: 2024-11-23T15:04:03.307Z Has data issue: false hasContentIssue false

Synergistic effect of basic fibroblast growth factor (bFGF) and epidermal growth factor on derivation of camel (Camelus dromedarius) trophoblast stem cells

Published online by Cambridge University Press:  20 June 2019

Faisal A. Alzahrani*
Affiliation:
Department of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah 21589, Kingdom of Saudi Arabia; and Department of Biological Sciences, Rabigh College of Science and Arts, King Abdulaziz University, Rabigh Branch, Rabigh 21911, Kingdom of Saudi Arabia
*
*Address for correspondence: Faisal A. Alzahrani. Department of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah 21589, Kingdom of Saudi Arabia; and Department of Biological Sciences, Rabigh College of Science and Arts, King Abdulaziz University, Rabigh Branch, Rabigh 21911, Kingdom of Saudi Arabia. E-mail: [email protected]

Summary

This study aimed to optimize the derivation of trophectoderm from in vitro-produced camel embryos under feeder-free culture conditions using the basement membrane matrix Matrigel. Trophoblastic vesicles were obtained through mechanical microdissection of in vitro-produced camel (Camelus dromedarius) embryos. Supplementing the culture medium with 10 ng/ml of epidermal growth factor and 10 ng/ml fibroblast growth factor improved the attachment and subsequent outgrowths of cultured trophoblastic vesicles when compared with the control group and the groups supplemented individually with each growth factor. The expression levels of pluripotency genes octamer-binding transcription factor 4 (Oct4), sex determining region Y-box 2 (Sox2), myelocytomatosis proto-oncogene (c-Myc) and anti-apoptotic gene B-cell lymphoma 2 (Bcl2) were increased in trophoblastic vesicles supplemented with both growth factors when compared with the control group. Conversely, both growth factors decreased the expression of apoptotic genes tumour protein p53 (p53) and Bcl-2-associated X protein (Bax). To the best of our knowledge, this may be the first report describing the derivation of trophoblast stem cells from in vitro-produced camel embryos.

Type
Short Communication
Copyright
© Cambridge University Press 2019 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Ahumada, CJ, Salvador, I, Cebrian-Serrano, A, Lopera, R and Silvestre, MA (2012) Effect of supplementation of different growth factors in embryo culture medium with a small number of bovine embryos on in vitro embryo development and quality. Animal 7, 455462.CrossRefGoogle ScholarPubMed
Armant, DR (2006) Blastocyst culture. In M. J. Soares and J. S. Hunt (eds). Placenta and Trophoblast: Methods and Protocols, Volume 1. Humana Press Inc., Totowa, NJ, USA. pp. 3556.Google Scholar
Blomberg, LA and Telugu, B (2012) Twenty years of embryonic stem cell research in farm animals. Reprod Domest Anim 47, 8085.CrossRefGoogle ScholarPubMed
Dean, W, Mohapatra, SK, Sandhu, A, Singh, KP, Singla, SK, Chauhan, MS, Manik, R and Palta, P (2015) Establishment of trophectoderm cell lines from buffalo (Bubalus bubalis) embryos of different sources and examination of in vitro developmental competence, quality, epigenetic status and gene expression in cloned embryos derived from them. PLoS One 10, e0129235.Google Scholar
Haimovici, F and Anderson, DJ (1993) Effects of growth factors and growth factor-extracellular matrix interactions on mouse trophoblast outgrowth in vitro . Biol Reprod 49, 124130.CrossRefGoogle ScholarPubMed
Kubaczka, C, Senner, C, Araúzo-Bravo, MJ, Sharma, N, Kuckenberg, P, Becker, A, Zimmer, A, Brüstle, O, Peitz, M, Hemberger, M and Schorle, H (2014) Derivation and maintenance of murine trophoblast stem cells under defined conditions. Stem Cell Rep 2, 232242.CrossRefGoogle ScholarPubMed
Kunath, T, Yamanaka, Y, Detmar, J, MacPhee, D, Caniggia, I, Rossant, J and Jurisicova, A (2014) Developmental differences in the expression of FGF receptors between human and mouse embryos. Placenta 35, 10791088.CrossRefGoogle ScholarPubMed
Latos, PA and Hemberger, M (2016) From the stem of the placental tree: trophoblast stem cells and their progeny. Development 143, 36503660.CrossRefGoogle ScholarPubMed
Lee, ES and Fukui, Y (1995) Effect of various growth factors in a defined culture medium on in vitro development of bovine embryos matured and fertilized in vitro . Theriogenology 44, 7183.CrossRefGoogle Scholar
Mohammadi-Sangcheshmeh, A, Shafiee, A, Seyedjafari, E, Dinarvand, P, Toghdory, A, Bagherizadeh, I, Schellander, K, Cinar, MU and Soleimani, M (2013) Isolation, characterization, and mesodermic differentiation of stem cells from adipose tissue of camel (Camelus dromedarius). In Vitro Cell Dev Biol Anim 49, 147154.CrossRefGoogle Scholar
Okae, H, Toh, H, Sato, T, Hiura, H, Takahashi, S, Shirane, K, Kabayama, Y, Suyama, M, Sasaki, H and Arima, T (2018) Derivation of human trophoblast stem cells. Cell Stem Cell 22, 5063.e56.CrossRefGoogle ScholarPubMed
Pan, Y, Cui, Y, Baloch, AR, He, H, Fan, J, He, J, Li, Q, Yang, K, Zhang, Q and Yu, S (2015) Epidermal growth factor enhances the developmental competence of yak (Bos grunniens) preimplantation embryos by modulating the expression of survivin and HSP70. Livest Sci 182, 118124.CrossRefGoogle Scholar
Peter, AT, Beg, MA, Ahmad, E and Bergfelt, DR (2017) Trophoblast of domestic and companion animals: basic and applied clinical perspectives. Anim Reprod 14, 12091224.CrossRefGoogle Scholar
Saadeldin, IM, Kim, SJ and Lee, BC (2015) Blastomeres aggregation as an efficient alternative for trophoblast culture from porcine parthenogenetic embryos. Dev Growth Differ 57, 362368.CrossRefGoogle ScholarPubMed
Saadeldin, IM, Swelum, AA, Elsafadi, M, Moumen, AF, Alzahrani, FA, Mahmood, A, Alfayez, M and Alowaimer, AN (2017a) Isolation and characterization of the trophectoderm from the Arabian camel (Camelus dromedarius) Placenta 57, 113122.CrossRefGoogle Scholar
Saadeldin, IM, Swelum, AA, Yaqoob, SH and Alowaimer, AN (2017b) Morphometric assessment of in vitro matured dromedary camel oocytes determines the developmental competence after parthenogenetic activation. Theriogenology 95, 141148.CrossRefGoogle Scholar
Saadeldin, IM, Abdel-Aziz Swelum, A, Alzahrani, FA and Alowaimer, AN (2018a) The current perspectives of dromedary camel stem cells research. Int J Vet Sci Med 6, S27S30.CrossRefGoogle Scholar
Saadeldin, IM, Swelum AA., -A, Elsafadi, M, Mahmood, A, Alfayez, M and Alowaimer, AN (2018b) Differences between the tolerance of camel oocytes and cumulus cells to acute and chronic hyperthermia. J Thermal Biol 74, 4754.CrossRefGoogle Scholar
Saadeldin, IM, Swelum, AA, Elsafadi, M, Mahmood, A, Alfayez, M and Alowaimer, AN (2018c) Cumulus cells of camel (Camelus dromedarius) antral follicles are multipotent stem cells. Theriogenology 118, 233242.CrossRefGoogle Scholar
Schmittgen, TD and Livak, KJ (2008) Analyzing real-time PCR data by the comparative CT method. Nat Protocol 3, 11011108.CrossRefGoogle Scholar
Shimada, A, Nakano, H, Takahashi, T, Imai, K and Hashizume, K (2001) Isolation and characterization of a bovine blastocyst-derived trophoblastic cell line, bt-1: development of a culture system in the absence of feeder cell. Placenta 22, 652662.CrossRefGoogle ScholarPubMed
Strom, S, Inzunza, J, Grinnemo, KH, Holmberg, K, Matilainen, E, Stromberg, AM, Blennow, E and Hovatta, O (2007) Mechanical isolation of the inner cell mass is effective in derivation of new human embryonic stem cell lines. Hum Reprod 22, 3051–308.CrossRefGoogle ScholarPubMed
Talbot, NC, Powell, AM, Camp, M and Ealy, AD (2007) Establishment of a bovine blastocyst-derived cell line collection for the comparative analysis of embryos created in vivo and by in vitro fertilization, somatic cell nuclear transfer, or parthenogenetic activation. In Vitro Cell Dev Biol Anim 43, 5971.CrossRefGoogle ScholarPubMed
Tanaka, S, Kunath, T, Hadjantonakis, AK, Nagy, A and Rossant, J (1998) Promotion of trophoblast stem cell proliferation by FGF4. Science 282, 20722075.CrossRefGoogle ScholarPubMed
Wutz, A, Tan, T, Tang, X, Zhang, J, Niu, Y, Chen, H, Li, B, Wei, Q and Ji, W (2011) Generation of trophoblast stem cells from rabbit embryonic stem cells with BMP4. PLoS One 6, e17124.Google Scholar
Yaqoob, SH, Saadeldin, IM, Swelum, AA.-A and Alowaimer, AN (2017) Optimizing camel (Camelus dromedarius) oocytes in vitro maturation and early embryo culture after parthenogenetic activation. Small Rum Res 153, 8186.CrossRefGoogle Scholar