| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Journal of Andrology, Vol 20, Issue 1 47-53, Copyright © 1999 by The American Society of Andrology
JOURNAL ARTICLE |
G. D. Smith, D. P. Wolf, K. C. Trautman and S. Vijayaraghavan
Division of Reproductive Sciences, Oregon Regional Primate Research Center, Beaverton, USA.
Human and monkey ejaculated sperm contain protein phosphatase-1 (PP1), PP1 inhibitor 2 (12), and glycogen synthase kinase-3 (GSK-3). Inhibition of ejaculated human sperm protein phosphatase (PP) activity with calyculin-a (CL-A) significantly stimulates motility, implicating protein dephosphorylation in motility regulation. The present experiments were conducted to characterize and compare PP and GSK-3 activity in monkey caput and caudal epididymal sperm, to determine the cellular distribution of these enzymes, and to test the thesis that epididymal sperm PP activity is inversely related to motility. Caput epididymal sperm populations, (8.8% motile) contained levels of PP activity that were >3 times as high as those of caudal spermatozoa. This PP activity was further identified by inhibitor response profiles as PP1. In both caput and caudal sperm, the majority of this PP1 activity was localized in 100,000 x g soluble fractions. Western blot analysis indicated that a portion of this difference was the result of elevated amounts of PP1 in caput compared with caudal epididymal sperm. The presence of GSK-3 activity was undetectable in 100,000 x g insoluble fractions of epididymal sperm, whereas both caput and caudal sperm soluble fractions contained GSK-3 activity, which was approximately threefold higher in caput sperm compared with caudal populations. Treatment of caput epididymal sperm from the rhesus macaque with the PP inhibitor CL-A resulted in a significant, dose-dependent increase from 8 to 38% motile cells (without any effect on their path velocity). In contrast, CL-A had no significant influence on either percent motility or path velocity of caudal epididymal sperm. Cytosolic PP1 and GSK-3 activities appear to be inversely related to the motility of monkey epididymal sperm and may have a regulatory role in the development of the potential for motility in epididymal sperm.
This article has been cited by other articles:
![]() |
Z. Huang, P. R. Somanath, R. Chakrabarti, E. M. Eddy, and S. Vijayaraghavan Changes in Intracellular Distribution and Activity of Protein Phosphatase PP1{gamma}2 and Its Regulating Proteins in Spermatozoa Lacking AKAP4 Biol Reprod, February 1, 2005; 72(2): 384 - 392. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. R. Somanath, S. L. Jack, and S. Vijayaraghavan Changes in Sperm Glycogen Synthase Kinase-3 Serine Phosphorylation and Activity Accompany Motility Initiation and Stimulation J Androl, July 1, 2004; 25(4): 605 - 617. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Huang, K. Myers, B. Khatra, and S. Vijayaraghavan Protein 14-3-3{zeta} Binds to Protein Phosphatase PP1{gamma}2 in Bovine Epididymal Spermatozoa Biol Reprod, July 1, 2004; 71(1): 177 - 184. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Huang and S. Vijayaraghavan Increased Phosphorylation of a Distinct Subcellular Pool of Protein Phosphatase, PP1{gamma}2, During Epididymal Sperm Maturation Biol Reprod, February 1, 2004; 70(2): 439 - 447. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Huang, B. Khatra, M. Bollen, D. W. Carr, and S. Vijayaraghavan Sperm PP1{gamma}2 Is Regulated by a Homologue of the Yeast Protein Phosphatase Binding Protein sds221 Biol Reprod, December 1, 2002; 67(6): 1936 - 1942. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. S. Tash, S. Kim, M. Schuber, D. Seibt, and W. H. Kinsey Fertilization of Sea Urchin Eggs and Sperm Motility Are Negatively Impacted under Low Hypergravitational Forces Significant to Space Flight Biol Reprod, October 1, 2001; 65(4): 1224 - 1231. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |