Published-Ahead-of-Print January 24, 2007, DOI:10.2164/jandrol.106.000869
Journal of Andrology, Vol. 28, No. 4, July/August 2007
Copyright © American Society of Andrology
DOI: 10.2164/jandrol.106.000869
Damage to Chromosomes and DNA of Rhesus Monkey Sperm Following Cryopreservation
MING-WEN LI*,
STUART MEYERS
,
THEODORE L. TOLLNER* AND
JAMES W. OVERSTREET*
From the * Division of Reproductive Biology,
Department of Obstetrics and Gynecology, School of Medicine and
Department of Anatomy, Physiology, and Cell
Biology, School of Veterinary Medicine, University of California, Davis,
Davis, California.
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Correspondence to: Dr Stuart Meyers, One Shields Avenue, Department of
Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine,
University of California, Davis, Davis, CA 95616 (e-mail:
smeyers{at}ucdavis.edu). |
Fresh and frozen-thawed rhesus monkey sperm were analyzed for DNA damage
using the comet assay and for chromosome damage by cytogenetic analysis after
intracytoplasmic sperm injection (ICSI) into mouse oocytes. The percentage of
fresh sperm with damaged DNA in ejaculated semen was 0 to 2.7% (n = 5).
Conventional cryopreservation and storage in liquid nitrogen caused DNA damage
in 25.3% to 43.7% of sperm; when sperm were frozen without cryoprotectants,
52.7% to 92.0% of thawed sperm had DNA damage. However, no significant
difference in chromosome damage was found between fresh sperm and
frozen-thawed sperm when motile sperm were selected for ICSI. The percentage
of sperm with abnormal karyotypes ranged from 0 to 8.3%. The most common
structural chromosomal abnormalities in fresh motile sperm and frozen-thawed
motile sperm were chromosome breaks or fragments. Our findings suggest that
genetically competent frozen-thawed macaque sperm can be selected for
fertilization by using only motile sperm for ICSI.
Key words: Macaque, spermatozoa, ICSI
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[Abstract]
[Full Text]
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Copyright © 2007 by The American Society of Andrology.