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Activin A Promotes the Proliferation of Chicken (Gallus gallus) Primordial Germ Cells via TGFβ/SMAD Signalling Pathway |
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Abstract Primordial germ cells (PGCs) are kind of cells which have the potential to differentiate into germ cells. To investigate the effect of activin A on the survival and proliferation of chicken (Gallus gallus) embryonic blood PGCs cultured in vitro, PGCs were isolated from stage 13~15 chicken embryonic blood, and then the cultured PGCs were identified using PGCs marker antibodies and marker genes. After addition of activin A (0 and 100 ng/mL) into complete medium for 48 h, the cell number, morphology and cell cycle were detected. To study the regulative mechanism of activin A in PGCs proliferation, the DNA methylation level of deleted in azoospermia-like (Dazl) gene was measured. The protein expression and phosphorylation of transforming growth factor-β (TGF-β) and SMAD2/3 were tested by Western blot. The results showed that PGCs isolated from chicken embryonic blood was distinct from blood cells with big nuclear and rich in glycogen particles. The purity of PGCs rapidly rised by treatment with red blood cell lysis buffer (ACK), from (0.026±0.005)% to (69.2±4.6)%. The high purity and excellent growing trend of PGCs was obtained by subculture. After subculture for 3 passages, PGCs was positive with stage specific embryonic antigen 1 (SSEA-1), chicken vasa homologue (CVH) and periodic acid Schiff reaction (PAS). The expression of pluripotent related genes, PouV, Nanog and sex determining region Y (SRY)-box 2 (Sox2), suggested that the biology characterist theics were well maintained in PGCs cultured in vitro. After treated with activin A, numbers of PGCs were significantly increased and the morphology of PGCs was better than that of control group, with clear boundaries and cubic morphology. And the mRNA expression of cyclin-dependent kinases (CDK2)/Cyclin D1 and CDK6/Cyclin E were obviously up-regulated. Flow cytometry analysis confirmed that PGCs populations treated with activin A displayed a significant increase in the proportion of S and G2 phase cells, which meant that there were more PGCs which entered into mitosis process than that of control group. The survival and proliferation ability of PGCs was enhanced by addition of 100 ng/mL activin A. Moreover, the ratio of Dazl gene mythelation was decreased from 94.7% in control group to 52.6% in activin A treated group. However, the mRNA expression of Dazl was significantly increased. The results indicated that activin A promoted PGCs proliferation by reducing the mythelation of Dazl gene. The protein expressions of TGF-β and SMAD2/3 were up-regulated and the phosphorylation of SMAD2/3 was activated when PGCs were treated with activin A. Collectively, these results suggested that activin A significantly promoted the survival and proliferation of PGCs cultured in vitro via TGF-β/SMAD signaling pathway and Dazl mythelation. These data provides basic information for the mechanism of PGCs proliferation regulated by activin A, and provides theoretical foundation to regulate germ cell development by using PGCs culture model.
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Received: 06 December 2016
Published: 31 March 2017
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Alak BM, Coskun S, Friedman CI, et al. 1998. Activin A stimulates meiotic maturation of human oocytes and modulates granulosa cell steroidogenesis in vitro[J]. Fertility and Sterility, 70(6):1126-1130.Anderson RA, Fulton N, Cowan G, et al. 2007. Conserved and divergent patterns of expression of DAZL, VASA and OCT4 in the germ cells of the human fetal ovary and testis[J]. BMC Developmental Biology, 7:136.Chang IK, Tajima A, Chikamune T, et al. 1995. Proliferation of Chick Primordial Germ-Cells Cultured on Stroma Cells from the Germinal Ridge[J]. Cell Biology International, 19(2):143-149.Cherny RA, Stokes TM, Merei J, et al. 1994. Strategies for the isolation and characterization of bovine embryonic stem cells[J]. Reproduction Fertility and Development, 6(5):569-575.Chiquoine AD. 1954. The identification, origin, and migration of the primordial germ cells in the mouse embryo[J]. Anatomical Record, 118(2):135-146. Coutts SM, Childs AJ, Fulton N, et al. 2008. Activin signals via SMAD2/3 between germ and somatic cells in the human fetal ovary and regulates kit ligand expression[J]. Developmental Biology, 314(1):189-199.Dias VL, Rajpert-De Meyts E, McLachlan R, et al. 2009. Analysis of activin/TGFB-signaling modulators within the normal and dysfunctional adult human testis reveals evidence of altered signaling capacity in a subset of seminomas[J]. Reproduction, 138(5):801-811.Fujimoto T, Ukeshima A, Kiyofuji R. 1976. The origin, migration and morphology of the primordial germ cells in the chick embryo[J]. Anatomical Record, 185(2):139-145.Gonzalez-Recio O, Toro MA, Bach A. 2015. Past, present, and future of epigenetics applied to livestock breeding[J]. Frontiers in Genetics, 6:305.Jorgensen A, Young J, Nielsen JE, et al. 2014. Hanging drop cultures of human testis and testis cancer samples: a model used to investigate activin treatment effects in a preserved niche[J]. British Journal of Cancer, 110(10):2604-2614.Jung JG, Kim DK, Park TS, et al. 2005. Development of novel markers for the characterization of chicken primordial germ cells[J]. Stem Cells, 23(5):689-698.Kehler J, Tolkunova E, Koschorz B, et al. 2004. Oct4 is required for primordial germ cell survival[J]. Embo Reports, 5(11):1078-1083.Kishi H, Minegishi T, Tano M, et al.1998. The effect of activin and FSH on the differentiation of rat granulosa cells[J]. FEBS Letters, 422(2):274-278.Kuwana T, Fujimoto T. 1984. Locomotion and scanning electron microscopic observations of primordial germ cells from the embryonic chick blood in vitro[J]. Anatomical Record, 209(3):337-343.Maratou K, Forster T, Costa Y, et al. 2004. Expression profiling of the developing testis in wild-type and Dazl knockout mice[J]. Mollecular Reproduction and Development, 67(1):26-54.Martins da Silva SJ, Bayne RA, Cambray N, et al. 2004. Expression of activin subunits and receptors in the developing human ovary: activin A promotes germ cell survival and proliferation before primordial follicle formation[J]. Developmental Biology, 266(2):334-345.McCarrey JR, Hsu KC, Eddy EM, et al. 1987. Isolation of viable mouse primordial germ cells by antibody-directed flow sorting[J]. Journal of Experimental Zoology, 242(1):107-111.Miles DC, Wakeling SI, Stringer JM, et al.2013. Signaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell development[J]. PLoS One, 8(1):e54606.Miro F, Hillier SG. 1996. Modulation of granulosa cell deoxyribonucleic acid synthesis and differentiation by activin[J]. Endocrinology, 137(2):464-468.Miyake A, Saito T, Kashiwagi N, et al.2006. Cloning and pattern of expression of the shiro-uo vasa gene during embryogenesis and its roles in PGC development[J]. International Journal of Developmental Biology, 50(7):619-625.Miyoshi N, Stel JM, Shioda K, et al. 2016. Erasure of DNA methylation, genomic imprints, and epimutations in a primordial germ-cell model derived from mouse pluripotent stem cells[J]. Proc Natl Acad Sci U S A, 113(34):9545-9550.Naito M, Tajima A, Tagami T, et al. 1994. Preservation of chick primordial germ cells in liquid nitrogen and subsequent production of viable offspring[J]. Journal of Reproduction and Fertility, 102(2):321-325.Okano M, Bell DW, Haber DA, et al. 1999. DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development[J]. Cell, 99(3):247-257.Petitte JN, Karagenc L, Ginsburg M. 1997. The origin of the avian germ line and transgenesis in birds[J]. Poultry Science, 76(8):1084-1092.Schmierer B, Schuster MK, Shkumatava A, et al. 2003. Activin and follicle-stimulating hormone signaling are required for long-term culture of functionally differentiated primary granulosa cells from the chicken ovary[J]. Biology of Reproduction, 68(2):620-627.Shim H, Gutierrez-Adan A, Chen LR, et al.1997. Isolation of pluripotent stem cells from cultured porcine primordial germ cells[J]. Biology of Reproduction, 57(5):1089-1095.Sun R, Sun YC, Ge W, et al.2015. The crucial role of Activin A on the formation of primordial germ cell-like cells from skin-derived stem cells in vitro[J]. Cell Cycle, 14(19):3016-3029.Thomson JA, Odorico JS. 2000. Human embryonic stem cell and embryonic germ cell lines[J]. Trends in Biotechnology, 18(2):53-57.Toyooka Y, Tsunekawa N, Akasu R, et al. 2003. Embryonic stem cells can form germ cells in vitro[J]. Proc Natl Acad Sci U S A, 100(20):11457-11462.Turnpenny L, Brickwood S, Spalluto CM, et al. 2003. Derivation of human embryonic germ cells: an alternative source of pluripotent stem cells[J]. Stem Cells, 21(5):598-609.van de Lavoir MC, Diamond JH, Leighton PA, et al. 2006. Germline transmission of genetically modified primordial germ cells[J]. Nature, 441(7094):766-769.Vanttinen T, Kuulasmaa T, Liu J, et al.2002. Expression of activin/inhibin receptor and binding protein genes and regulation of activin/inhibin peptide secretion in human adrenocortical cells[J]. J Clin Endocrinol Metab 87(9):4257-4263.von Meyenn F, Berrens RV, Andrews S, et al. 2016. Comparative Principles of DNA Methylation Reprogramming during Human and Mouse In Vitro Primordial Germ Cell Specification[J]. Dev Cell 39(1):104-115.Wentworth BC, Tsai H, Hallett JH, et al. 1989. Manipulation of avian primordial germ cells and gonadal differentiation[J]. Poult Sci 68(7):999-1010. |
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