Welcome to Open Science
Contact Us
Home Books Journals Submission Open Science Join Us News
Study of DNA Fragmentation in Gametes of Infertile Male by Using TUNEL Technique
Current Issue
Volume 5, 2017
Issue 6 (December)
Pages: 47-50   |   Vol. 5, No. 6, December 2017   |   Follow on         
Paper in PDF Downloads: 70   Since Sep. 24, 2017 Views: 1324   Since Sep. 24, 2017
Authors
[1]
Ouafia Liamani, Department of Biology, Faculties of Nature and Life Sciences, Djillali Liabes University, Sidi Bel Abbes, Algeria.
[2]
Soraya Moulessehoul, Department of Biology, Faculties of Nature and Life Sciences, Djillali Liabes University, Sidi Bel Abbes, Algeria.
[3]
Ismat Benzeguir, Laboratory of Analysis of Medical Biology, Sidi Bel Abbes, Algeria.
Abstract
Male factors leading to infertility account for at least half of all cases of infertility worldwide. In this study, we used Terminal desoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) assay to evaluate DNA fragmentation in sperm cells. The study group included 12 males with infertility and oligoasthenoteratozoospermia (OATs). The mean DNA fragmentation index was significantly higher in patients compared to the control group. In conclusion the TUNEL may be considered as an additional assay for the evaluation of spermatozoa beside standard analysis, thus playing an important role during proper diagnosis and treatment of infertility. As in these days, for patients with OAT, intracytoplasmic sperm injection (ICSI) is frequently used.
Keywords
Oligoasthenoteratozoospermia, DNA Fragmentation, TUNEL
Reference
[1]
Aitken RJ, Baker MA, Sawyer D (2003) Oxidative stress in the male germ line and its role in the aetiology of male infertility and genetic disease. Reprod Biomed Online 7:65–70.
[2]
Bakos HW, Thompson JG, Feil D, Lane M (2007) Sperm DNA damage is associated with assisted reproductive technology pregnancy. Int J Androl 30:1–9.
[3]
Bennetts LE & Aitken RJ. (2005) A comparative study of oxidative DNA damage in mammalian spermatozoa. Mol Reprod Dev 71, 77–87.
[4]
Bennetts LE & Aitken RJ. (2005) A comparative study of oxidative DNA damage in mammalian spermatozoa. Mol Reprod Dev 71, 77–87.
[5]
Brahem S, Mehdi M, Elghezal H, Saad A, Detection of DNA fragmentation and meiotic segregation in human with isolated teratozoospermia. J Assist Reprod Genet. 2011; 28(1):41-8.
[6]
Chatzimeletiou K, ioga A, Oikonomou L, Charalampidou S, Kantartzi P, Zournatzi V. Semen analysis by electron and fluorescence microscopy in a case of partial hydatidiform mole reveals a high incidence of abnormal morphology, diploidy, and tetraploidy. Fertil Steril. 2011; 95(7):2430.e1-5.
[7]
Dunkel L, Hirvonen V & Erkkila K. (1997) Clinical aspects of male germ cell apoptosis during testis development and spermatogenesis. Cell Death Differ 4, 171–179.
[8]
Evenson DP, Darzynkiewicz Z, Melamed MR (1980) Relation of mammalian sperm chromatin heterogeneity to fertility. Science 240:1131–1133.
[9]
Garolla A et al. High-power microscopy for selecting spermatozoa for ICSI by physiological status. Reprod Biomed Online. 2008; 17(5):610-6.
[10]
Greco E, Scarselli F, Iacobelli M, Rienzi L, Ubaldi F, Ferrero S, Franco G, Anniballo N, Mendoza C, Tesarik J. Efficient treatment of infertility due to sperm DNA damage by ICSI with testicular spermatozoa. Hum Reprod 2005;20:226–230.
[11]
Henkel R, Hajmohamed M, Stalf T, Hougendijk C, Mehnert C, Menkveld R, Gips H, Schill WB, Kurger TF (2004) Influence of deoxyribonucleic acid damage on fertilization and pregnancy. Fertil Steril 81:965–972.
[12]
Henkel R, Maaß G, Hajimohammad M, Menkveld R, Stalf T, Villegas J, Sa´nchez R, Kruger TF, Schill WB (2003) Urogenital inflammation: changes of leucocytes and ROS. Andrologia 35:309–313.
[13]
Irvine DS, Twigg JP, Gordon EL, Fulton N, Milne PA & Aitken RJ. (2000) DNA integrity in human spermatozoa: relationships with semen quality. J Androl 21, 33–44.
[14]
Lee J, Richburg JH, Younkin SC & Boekelheide K. (1997) The Fas system is a key regulator of germ cell apoptosis in the testis. Endocrinology 138, 2081–2088.
[15]
Lin HH, Lee RK, Li SH, Lu CH, Sun FJ, Hwu YM. Sperm chromatin structure assay parameters are not related to fertilization rates, embryo quality, and pregnancy rates in in vitro fertilization and intracytoplasmic sperm injection, but might be related to spontaneous abortion rates. Fertil Steril 2008; 90:352–359.
[16]
Liu CH et al. DNA fragmentation, mitochondrial dysfunction and chromosomal aneuploidy in the spermatozoa of oligoasthenoteratozoospermic males. J Assist Reprod Genet. 2004;21(4):119-26.
[17]
Mehdi M, Khantouche L, Ajina M, Saad A. Detection of DNA fragmentation in human spermatozoa: correlation with semen parameters. Andrologia. 2009; 41(6):383–6.
[18]
Nicopoullos JDM, Ramsay JWA, Almeida P, Gilling-Smith C. (2005) Can the outcome of intracytoplasmic sperm injection be predicted by genetic screening of spermatozoa? Abstracts of the 21st annual meeting of the European Society for Human Reproduction and Embryology. June 19–22, 2005, Copenhagen. Denmark, i198.
[19]
Nijs M, Creemers E, Cox A, Franssen K, Janssen M, Vanheusden E, de Jonge C, Ombelet W. Chromomycin A3 staining, sperm chromatin structure assay and hyaluronic acid binding assay as predictors for assisted reproductive outcome. Reprod Biomed Online 2009;19:671–684.
[20]
Ovári L et al. Double probing individual human spermatozoa: aniline blue staining for persistent histones and fluorescence in situ hybridization for aneuploidies. Fertil Steril. 2010;93(7):2255-61.
[21]
Ozmen B, Caglar GS, Koster F, Schopper B, Diedrich K, Al-Hasani S. Relationship between sperm DNA damage, induced acrosome reaction and viability in ICSI patients. Reprod Biomed Online 2007a; 15:208–214.
[22]
Ozmen B, Koutlaki N, Youssry M, Diedrich K & Al-Hasani S. (2007b) DNA damage of human spermatozoa in assisted reproduction: origins, diagnosis, impacts and safety. Reprod Biomed Online 14, 384–395.
[23]
Perrin A., Nguyen M. H., Bujan L., Vialard F., Amice V., Gu_eganic N., Douet-Guilbert N., De Braekeleer M. Morel F. 2013 DNA fragmentation is higher in spermatozoa with chromosomally unbalanced content in men with a structural chromosomal rearrangement Andrology, 1, 632–638.
[24]
Sá R, Sousa M. Sperm aneuploidy and DNA integrity: a review. Reproductive health 2015 EMJ european medical journal. 1[1]:65-73.
[25]
Sakkas D, Mariethoz E, Manicardi G, Bizzaro D, Bianchi PG & Bianchi U. (1999) Origin of DNA damage in ejaculated human spermatozoa. Rev Reprod 4, 31–37.
[26]
Sakkas D, Moffatt O, Manicardi GC, Mariethoz E, Tarozzi N & Bizzaro D. (2002) Nature of DNA damage in ejaculated human spermatozoa and the possible involvement of apoptosis. Biol Reprod 66, 1061– 1067.
[27]
Sergerie M, Laforest G, Bujan L, Bissonnette F & Bleau G. (2005) Sperm DNA fragmentation: threshold value in male fertility. Hum Reprod 20, 3446–3451.
[28]
Shamsi MB, Kumar R, Dada R (2008) Evaluation of nuclear DNA damage in human spermatozoa in men opting for assisted reproduction. Indian J Med Res 127:115–123.
[29]
Sinha Hikim AP & Swerdloff RS. (1999) Hormonal and genetic control of germ cell apoptosis in the testis. Rev Reprod 4, 38–47.
[30]
Tang SS et al. Aneuploidy and DNA fragmentation in morphologically abnormal sperm. Int J Androl. 2010;33(1):e163-79.
[31]
Tesarik J. 2005. Paternal effects on cell division in the human preimplantation embryo. Reprod Biomed Online;10: 370-375.
[32]
Tavalaee M, Razavi S, Nasr-Esfahani MH. Influence of sperm chromatin anomalies on assisted reproductive technology outcome. Fertil Steril 2009;91:1119–1126.
[33]
World Health Organization. WHO laboratory manual for the examination and processing of human semen. 5th edition. Available at: http://whqlibdoc.who.int/ publications/2010/9789241547789_eng. pdf. Last accessed: 6 June 2015.
[34]
Zini A, Bielecki R, Phang D, Zenzes MT (2001) Correlations between two markers of sperm DNA integrity, DNA denaturation and DNA fragmentation, infertile and in fertilemen. Fertil Steril7 5: 674–677.
[35]
Zini A, Meriano J, Kader K, Jarvi K, Laskin CA, Cadesky K. Potential adverse effect of sperm DNA damage on embryo quality after ICSI. Hum Reprod 2005; 20:3476–3480.
Open Science Scholarly Journals
Open Science is a peer-reviewed platform, the journals of which cover a wide range of academic disciplines and serve the world's research and scholarly communities. Upon acceptance, Open Science Journals will be immediately and permanently free for everyone to read and download.
CONTACT US
Office Address:
228 Park Ave., S#45956, New York, NY 10003
Phone: +(001)(347)535 0661
E-mail:
LET'S GET IN TOUCH
Name
E-mail
Subject
Message
SEND MASSAGE
Copyright © 2013-, Open Science Publishers - All Rights Reserved