Journal of Andrology Testis Workshop 2009
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH

Published-Ahead-of-Print August 23, 2006, DOI:10.2164/jandrol.106.000216

This Article
Right arrow Author Manuscript (PDF)
Right arrow All Versions of this Article:
28/1/92    most recent
Author Manuscript (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Author home page(s):
W. Plummer
J. Diehl
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sutovsky, P.
Right arrow Articles by Sutovsky, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sutovsky, P.
Right arrow Articles by Sutovsky, M.

Relative Levels of Semen Platelet Activating Factor-Receptor (PAFr) and Ubiquitin in Yearling Bulls with High Content of Semen White Blood Cells: Implications for Breeding Soundness Evaluation

P. Sutovsky *, W. Plummer , K. Baska , K. Peterman , J. Diehl , and M. Sutovsky

* To whom correspondence should be addressed. E-mail: sutovskyp{at}missouri.edu.

High content of the platelet activating factor (PAF) and its plasma membrane receptor (PAFr) in semen is thought to benefit fertility in farm animals and humans. We used flow cytometric, biochemical and immunocytochemical analysis to examine PAFr levels alone (Trial 1; n=156 bulls) or in a dual assay with sperm defect marker ubiquitin (UBI; Trial 2, n=88 bulls), in semen samples from 160 yearling bulls undergoing Breeding Soundness Evaluations (BSE). In both trials, we observed increased PAFr levels in semen samples with high content of white blood cells (WBC). Consequently, PAFr levels within such semen samples correlated negatively with several subjective parameters of BSE including palpation, satisfaction of evaluation and scrotal circumference. Due to a high WBC content, increased semen sample dilution had to be applied for microscopic evaluation. There was a negative correlation between semen PAFr and conventional sperm morphology, while the increased levels of PAFr correlated positively with sperm UBI-content. Immunofluorescence microcopy revealed high expression of PAFr on the surface of leukocytes and morphologically normal spermatozoa, while reduced immunoreactivity was observed in defective spermatozoa immunoreactive to anti-UBI antibodies. A single PAFr band of appropriate mass was observed in Western blots of ejaculated spermatozoa while testicular and epididymal spermatozoa also displayed several larger bands indicative of postranslational processing or modification. Collectively, these data suggest that high levels of semen PAFr in young bulls are indicative of semen contamination with WBC. In the future, objective protein marker based semen analyses in young bulls will likely require additional parameters distinguishing between marker expression in the spermatozoa and in the contaminating WBC. While identification of high sperm PAFr levels may support fertility, this assay alone is not reliable due to the expression of PAFr in WBC that contaminate semen samples.



Key words: Fertility • Semen • Semen Analysis • Sperm




This article has been cited by other articles:


Home page
ReproductionHome page
P. Sarradin, S. Melo, C. Barc, C. Lecomte, O. Andreoletti, F. Lantier, J.-L. Dacheux, and J.-L. Gatti
Semen from scrapie-infected rams does not transmit prion infection to transgenic mice
Reproduction, March 1, 2008; 135(3): 415 - 418.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2006 by The American Society of Andrology.