TY - JOUR
T1 - Sperm artificially exposed to antisperm antibodies show altered deoxyribonucleic acid
AU - Evans, Michele L.
AU - Chan, Philip J.
AU - Patton, William C.
AU - King, Alan
N1 - PURPOSE:Our purpose was to assess sperm deoxyribonucleic acid (DNA) integrity after exposure to antisperm antibodies. METHODS:Donor semen were divided and exposed to sera containing IgG, IgA, and IgM antisperm antibodies. Untreated portions served as the control. After incubation (1 hr, 23 degrees C), the sperm were centrifuge-washed, resuspended, and incubated (23 degrees C) for 2, 5, 7, or 9 days.
PY - 1999
Y1 - 1999
N2 - Purpose: Our purpose was to assess sperm deoxyribonucleic acid (DNA) integrity after exposure to antisperm antibodies. Methods: Donor semen were divided and exposed to sera containing IgG, IgA, and IgM antisperm antibodies. Untreated portions served as the control. After incubation (I hr, 23°C), the sperm were centrifuge-washed, resuspended, and incubated (23°C) for 2, 5, 7, or 9 days. Acridine orange staining and kinematic parameters were measured. The sentinel (17q21 from D17S855) and β-globin genes were amplified and analyzed using denaturing gradient gel electrophoresis. Results: Sperm preexposed to antisperm antibodies had deleted sentinel gene on days 7 and 9. The β-globin gene was intact. There were no differences in acridine orange staining. Conclusions: Sperm artificially exposed to antisperm antibodies resulted in a subtle deletion of genetic material. The DNA alteration process was slow and was undetectable at the gross level. More studies are needed to confirm the findings and determine whether DNA repair mechanisms can reverse the damage.
AB - Purpose: Our purpose was to assess sperm deoxyribonucleic acid (DNA) integrity after exposure to antisperm antibodies. Methods: Donor semen were divided and exposed to sera containing IgG, IgA, and IgM antisperm antibodies. Untreated portions served as the control. After incubation (I hr, 23°C), the sperm were centrifuge-washed, resuspended, and incubated (23°C) for 2, 5, 7, or 9 days. Acridine orange staining and kinematic parameters were measured. The sentinel (17q21 from D17S855) and β-globin genes were amplified and analyzed using denaturing gradient gel electrophoresis. Results: Sperm preexposed to antisperm antibodies had deleted sentinel gene on days 7 and 9. The β-globin gene was intact. There were no differences in acridine orange staining. Conclusions: Sperm artificially exposed to antisperm antibodies resulted in a subtle deletion of genetic material. The DNA alteration process was slow and was undetectable at the gross level. More studies are needed to confirm the findings and determine whether DNA repair mechanisms can reverse the damage.
KW - Antisperm antibodies
KW - Apoptosis
KW - Denaturing gradient gel electrophoresis
KW - Immunology
KW - Spermatozoa
UR - https://www.scopus.com/pages/publications/0032843873
UR - https://www.scopus.com/pages/publications/0032843873#tab=citedBy
U2 - 10.1023/A:1020525726674
DO - 10.1023/A:1020525726674
M3 - Article
C2 - 10478325
SN - 1058-0468
VL - 16
SP - 443
EP - 449
JO - Journal of Assisted Reproduction and Genetics
JF - Journal of Assisted Reproduction and Genetics
IS - 8
ER -