DNA integrity in sexed bull sperm assessed by neutral Comet assay and sperm chromatin structure assay

被引:88
作者
Boe-Hansen, GB
Morris, ID
Ersboll, AK
Greve, T
Christensen, P
机构
[1] Royal Vet & Agr Univ, Dept Large Anim Sci Vet Reprod & Obstet, DK-1870 Frederiksberg, Copenhagen, Denmark
[2] Univ York, Dept Biol, Hull York Med Sch, York YO10 5DD, N Yorkshire, England
关键词
flow cytometry; single cell gel electrophoresis; sex sorting spermatozoa; bovine; DNA;
D O I
10.1016/j.theriogenology.2004.08.004
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
During the production of sex-sorted spermatozoa from bull semen, the cells are exposed to a number of potential hazards including: dilution, centrifugation, incubation, exposure to DNA stains and laser light. These factors may affect the survival capacity and fertilization potential of the sperm. The objective of this study was to determine whether sex-sorted bull spermatozoa have more DNA damage than sperm from conventional processed bull semen. Two methods were used 0 to determine DNA integrity: the neutral Comet assay (NCA) and the sperm chromatin structure assay (SCSA). The NCA showed that the conventional samples had a higher tail moment (TM) (P < 0.017) than the sorted samples and that there was no difference between the samples in tail length (TL) (P = 0.36). The SCSA showed that the DNA fragmentation index (DFI) was higher for conventional than the sorted samples (P = 0.011), but the standard deviation of DFI (SD-DFI) was higher for the sorted samples (P < 0.001). We conclude that the NCA and SCSA can be used in assessing DNA integrity in bovine sperm and that cell sorting by flow cytometry improves the integrity of the sperm cell population. Additionally the results from the SCSA indicated that the sex-sorted sperm had less homogenous sperm chromatin. In the future assessment of sperm DNA integrity may be used to select bulls for sperm sex sorting and optimizing sperm sex sorting procedures. (c) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1789 / 1802
页数:14
相关论文
共 39 条
[1]   Susceptibility of human sperm to in situ DNA denaturation is strongly correlated with DNA strand breaks identified by single-cell electrophoresis [J].
Aravindan, GR ;
Bjordahl, J ;
Jost, LK ;
Evenson, DP .
EXPERIMENTAL CELL RESEARCH, 1997, 236 (01) :231-237
[2]   DNA repair mechanisms and gametogenesis [J].
Baarends, WM ;
van der Laan, R ;
Grootegoed, JA .
REPRODUCTION, 2001, 121 (01) :31-39
[3]   A MODEL FOR THE STRUCTURE OF CHROMATIN IN MAMMALIAN SPERM [J].
BALHORN, R .
JOURNAL OF CELL BIOLOGY, 1982, 93 (02) :298-305
[4]   HETEROGENEITY OF SPERM NUCLEAR CHROMATIN STRUCTURE AND ITS RELATIONSHIP TO BULL FERTILITY [J].
BALLACHEY, BE ;
HOHENBOKEN, WD ;
EVENSON, DP .
BIOLOGY OF REPRODUCTION, 1987, 36 (04) :915-925
[5]  
BALLACHEY BE, 1988, J ANDROL, V9, P109
[6]  
Bench GS, 1996, CYTOMETRY, V23, P263, DOI 10.1002/(SICI)1097-0320(19960401)23:4<263::AID-CYTO1>3.3.CO
[7]  
2-9
[8]   Sperm chromatin structure assay of bulls qualified for artificial insemination [J].
Bochenek, M ;
Smorag, Z ;
Pilch, J .
THERIOGENOLOGY, 2001, 56 (04) :557-567
[9]   Hoechst staining and exposure to UV laser during flow cytometric sorting does not affect the frequency of detected endogenous DNA nicks in abnormal and normal human spermatozoa [J].
Catt, SL ;
Sakkas, D ;
Bizzaro, D ;
Bianchi, PG ;
Maxwell, WMC ;
Evans, G .
MOLECULAR HUMAN REPRODUCTION, 1997, 3 (09) :821-825
[10]   Production of reactive oxygen species by spermatozoa undergoing cooling, freezing, and thawing [J].
Chatterjee, S ;
Gagnon, C .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 2001, 59 (04) :451-458