The Epigenetic Assessment of Human Spermatogenic Cells Derived from Obstructive Azoospermic Patients in Different Culture Systems
Urology Journal,
Vol. 18 No. 02 (2021),
,
Page 214-224
https://doi.org/10.22037/uj.v16i7.6092
Abstract
Purpose: Generating functional gametes for patients with male infertility is of great interest. We investigated different cultural systems for proliferation of SSCs derived from obstructive azoospermic patients.
Materials and Methods: Testicular cells were obtained from men with obstructive azoospermia. After enzymatic digestion process, cells were assigned to various groups: culture of SSCs in the dish without cover (control group), co-culture of SSCs with infertile Sertoli cells (I), co-culture of SSCs with fertile Sertoli cells (II), culture of SSCs on nanofiber (covered with laminin) (III), culture of testicular cell suspension (IV). Then cells were cultured and colony formation, gene-specific methylation (by MSP), quantitative genes expression of pluripotency (Nanog, C-Myc, Oct-4) and specific germ cell (Integrin α6, Integrin β1, PLZF) genes were evaluated in five different culture systems.
Results: Our findings indicate a significant increase in the number and diameter of colonies in IV group in compare to control group and other groups. Expression of germ specific genes in IV group were significantly increased (P ≤ 0.05) and levels of expression of pluripotency genes were significantly decreased in this group (P ≤ 0.05) compared with other groups. Gene-specific pattern of methylation of examined genes showed no changes in culture systems during the culture era.
Conclusion: A microenvironment capable of controlling the proliferation of cell colonies can be restored by testicular cell suspension.
- Spermatogonial Stem Cells
- proliferation
- testicular cell suspension
- Obstructive Azoospermia
How to Cite
References
Stukenborg J-B, Kjartansdóttir KR, Reda A, Colon E, Albersmeier JP, Söder O. Male germ cell development in humans. Hormone research in paediatrics. 2014;81:2-12.
Eslahi N, Hadjighassem MR, Joghataei MT, et al. The effects of poly L-lactic acid nanofiber scaffold on mouse spermatogonial stem cell culture. International journal of nanomedicine. 2013;8:4563.
Sadri-Ardekani H, Mizrak SC, van Daalen SK, et al. Propagation of human spermatogonial stem cells in vitro. Jama. 2009;302:2127-34.
Jones DL, Wagers AJ. No place like home: anatomy and function of the stem cell niche. Nature reviews Molecular cell biology. 2008;9:11.
Meng X, Lindahl M, Hyvönen ME, et al. Regulation of cell fate decision of undifferentiated spermatogonia by GDNF. Science. 2000;287:1489-93.
Kubota H, Avarbock MR, Brinster RL. Growth factors essential for self-renewal and expansion of mouse spermatogonial stem cells. Proceedings of the National Academy of Sciences. 2004;101:16489-94.
Yoshida S, Sukeno M, Nabeshima Y-i. A vasculature-associated niche for undifferentiated spermatogonia in the mouse testis. Science. 2007;317:1722-6.
Oatley JM, Brinster RL. The germline stem cell niche unit in mammalian testes. Physiological reviews. 2012;92:577-95.
Handel MA, Eppig JJ, Schimenti JC. Applying “gold standards” to in-vitro-derived germ cells. Cell. 2014;157:1257-61.
Hu Z, Xia Y, Guo X, et al. A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. Nature genetics. 2012;44:183.
Sun M, Yuan Q, Niu M, et al. Efficient generation of functional haploid spermatids from human germline stem cells by three-dimensional-induced system. Cell Death & Differentiation. 2018;25:747.
Hunter D, Anand-Ivell R, Danner S, Ivell R. Models of in vitro spermatogenesis. Spermatogenesis. 2012;2:32-43.
Sadri-Ardekani H, Akhondi MA, van der Veen F, Repping S, van Pelt AM. In vitro propagation of human prepubertal spermatogonial stem cells. Jama. 2011;305:2416-8.
Riboldi M, Rubio C, Pellicer A, Gil-Salom M, Simón C. In vitro production of haploid cells after coculture of CD49f+ with Sertoli cells from testicular sperm extraction in nonobstructive azoospermic patients. Fertility and sterility. 2012;98:580-90. e4.
Nagano MC. Techniques for culturing spermatogonial stem cells continue to improve. Biology of reproduction. 2011;84:5-6.
Stukenborg JB, Wistuba J, Luetjens CM, et al. Coculture of spermatogonia with somatic cells in a novel three‐dimensional soft‐agar‐culture‐system. Journal of andrology. 2008;29:312-29.
Stukenborg J-B, Schlatt S, Simoni M, et al. New horizons for in vitro spermatogenesis? An update on novel three-dimensional culture systems as tools for meiotic and post-meiotic differentiation of testicular germ cells. Molecular human reproduction. 2009;15:521-9.
Stukenborg J-B, Jahnukainen K. In vitro Spermatogenesis and Its Potential Clinical Implication for Patients. Genetics of Human Infertility. Vol 21: Karger Publishers; 2017:162-72.
Nickkholgh B, Mizrak SC, Van Daalen SK, et al. Genetic and epigenetic stability of human spermatogonial stem cells during long-term culture. Fertility and sterility. 2014;102:1700-7. e1.
Valli H, Sukhwani M, Dovey SL, et al. Fluorescence-and magnetic-activated cell sorting strategies to isolate and enrich human spermatogonial stem cells. Fertility and sterility. 2014;102:566-80. e7.
Hai Y, Hou J, Liu Y, et al. The roles and regulation of Sertoli cells in fate determinations of spermatogonial stem cells and spermatogenesis. Paper presented at: Seminars in cell & developmental biology, 2014.
Albert S, Wistuba J, Eildermann K, et al. Comparative marker analysis after isolation and culture of testicular cells from the immature marmoset. Cells Tissues Organs. 2012;196:543-54.
Anderson RA, Mitchell RT, Kelsey TW, Spears N, Telfer EE, Wallace WHB. Cancer treatment and gonadal function: experimental and established strategies for fertility preservation in children and young adults. The lancet Diabetes & endocrinology. 2015;3:556-67.
Galdon G, Atala A, Sadri-Ardekani H. In vitro spermatogenesis: how far from clinical application? Current urology reports. 2016;17:49.
Giudice MG, De Michele F, Poels J, Vermeulen M, Wyns C. Update on fertility restoration from prepubertal spermatogonial stem cells: how far are we from clinical practice? Stem cell research. 2017;21:171-7.
Shams A, Eslahi N, Movahedin M, Izadyar F, Asgari H, Koruji M. Future of spermatogonial stem cell culture: application of nanofiber scaffolds. Current stem cell research & therapy. 2017;12:544-53.
Ganjibakhsh M, Mehraein F, Koruji M, Aflatoonian R, Farzaneh P. Three-dimensional decellularized amnion membrane scaffold as a novel tool for cancer research; cell behavior, drug resistance and cancer stem cell content. Materials Science and Engineering: C. 2019;100:330-40.
Liu S, Tang Z, Xiong T, Tang W. Isolation and characterization of human spermatogonial stem cells. Reproductive Biology and Endocrinology. 2011;9:1.
Kanatsu-Shinohara M, Ogonuki N, Inoue K, et al. Long-term proliferation in culture and germline transmission of mouse male germline stem cells. Biology of reproduction. 2003;69:612-6.
Huleihel M, Fadlon E, AbuElhija A, Haber EP, Lunenfeld E. Glial cell line-derived neurotrophic factor (GDNF) induced migration of spermatogonial cells in vitro via MEK and NF-kB pathways. Differentiation. 2013;86:38-47.
Sada A, Hasegawa K, Pin PH, Saga Y. NANOS2 Acts Downstream of Glial Cell Line‐Derived Neurotrophic Factor Signaling to Suppress Differentiation of Spermatogonial Stem Cells. Stem Cells. 2012;30:280-91.
Tournaye H, Dohle GR, Barratt CL. Fertility preservation in men with cancer. The Lancet. 2014;384:1295-301.
Chen H-F, Ho H-N, Chen S-U, et al. Andrology: Co-culture with Vero cell monolayer maintains the motility of asthenozoospermic semen samples. Human Reproduction. 1994;9:1276-80.
Kanatsu-Shinohara M, Miki H, Inoue K, et al. Long-term culture of mouse male germline stem cells under serum-or feeder-free conditions. Biology of reproduction. 2005;72:985-91.
Koruji M, Movahedin M, Mowla S, Gourabi H, Arfaee A. Efficiency of adult mouse spermatogonial stem cell colony formation under several culture conditions. In Vitro Cellular & Developmental Biology-Animal. 2009;45:281.
Tajik P, Kohsari H, Qasemi-Panahi B, Sohrabi-Haghdoost I, Barin A, Ghasemzadeh-Nava H. Effects of Gonadotropin Releasing Hormone (GnRH) on bovine spermatogonial stem cell proliferationatogonial stem cells proliferation. Iranian Journal of Veterinary Science and Technology. 2015;6:11-20.
Bahadorani M, Hosseini S, Abedi P, et al. Short-term in-vitro culture of goat enriched spermatogonial stem cells using different serum concentrations. Journal of assisted reproduction and genetics. 2012;29:39-46.
Pramod RK, Mitra A. In vitro culture and characterization of spermatogonial stem cells on Sertoli cell feeder layer in goat (Capra hircus). Journal of assisted reproduction and genetics. 2014;31:993-1001.
Nowroozi MR, Ahmadi H, Rafiian S, Mirzapour T, Movahedin M. In vitro colonization of human spermatogonia stem cells: effect of patient's clinical characteristics and testicular histologic findings. Urology. 2011;78:1075-81.
Richardson LL, Kleinman HK, Dym M. Basement membrane gene expression by Sertoli and peritubular myoid cells in vitro in the rat. Biology of reproduction. 1995;52:320-30.
Mincheva M, Sandhowe-Klaverkamp R, Wistuba J, et al. Reassembly of adult human testicular cells: can testis cord-like structures be created in vitro? MHR: Basic science of reproductive medicine. 2017;24:55-63.
Schlatt S, de Kretser DM, Loveland KL. Discriminative analysis of rat Sertoli and peritubular cells and their proliferation in vitro: evidence for follicle-stimulating hormone-mediated contact inhibition of Sertoli cell mitosis. Biology of reproduction. 1996;55:227-35.
Lee BN, Kim DY, Kang HJ, et al. In vivo biofunctionality comparison of different topographic PLLA scaffolds. Journal of Biomedical Materials Research Part A. 2012;100:1751-60.
Ghaedi M, Soleimani M, Shabani I, Duan Y, Lotfi AS. Hepatic differentiation from human mesenchymal stem cells on a novel nanofiber scaffold. Cellular & molecular biology letters. 2012;17:89-106.
Delgado-Rivera R, Harris SL, Ahmed I, et al. Increased FGF-2 secretion and ability to support neurite outgrowth by astrocytes cultured on polyamide nanofibrillar matrices. Matrix Biology. 2009;28:137-47.
Koruji M, Shahverdi A, Janan A, Piryaei A, Lakpour MR, Sedighi MAG. Proliferation of small number of human spermatogonial stem cells obtained from azoospermic patients. Journal of assisted reproduction and genetics. 2012;29:957-67.
Lim J, Sung SY, Kim H, et al. Long‐term proliferation and characterization of human spermatogonial stem cells obtained from obstructive and non‐obstructive azoospermia under exogenous feeder‐free culture conditions. Cell proliferation. 2010;43:405-17.
Maitra A, Arking DE, Shivapurkar N, et al. Genomic alterations in cultured human embryonic stem cells. Nature genetics. 2005;37:1099.
Liu AM, Qu WW, Liu X, Qu C-K. Chromosomal instability in in vitro cultured mouse hematopoietic cells associated with oxidative stress. American journal of blood research. 2012;2:71.
Skinner MK. Environmental epigenomics and disease susceptibility. EMBO reports. 2011;12:620-2.
Bernardo ME, Zaffaroni N, Novara F, et al. Human bone marrow–derived mesenchymal stem cells do not undergo transformation after long-term in vitro culture and do not exhibit telomere maintenance mechanisms. Cancer research. 2007;67:9142-9.
Wang L, Yang Y, Zhu Y, et al. Characterization of placenta-derived mesenchymal stem cells cultured in autologous human cord blood serum. Molecular medicine reports. 2012;6:760-6.
Kanatsu-Shinohara M, Ogonuki N, Iwano T, et al. Genetic and epigenetic properties of mouse male germline stem cells during long-term culture. Development. 2005;132:4155-63.
Chikhovskaya J, Jonker M, Meissner A, Breit T, Repping S, van Pelt A. Human testis-derived embryonic stem cell-like cells are not pluripotent, but possess potential of mesenchymal progenitors. Human Reproduction. 2011;27:210-21.
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