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PMID: 9047017 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Regulation of protein tyrosine phosphorylation during bovine sperm capacitation by a cyclic adenosine 3'5'-monophosphate-dependent pathway.

Biology of reproduction ·Vol. 56 ·No. 3 ·1997-03-00 ·Pages 707-19

Galantino-Homer HL, Visconti PE, Kopf GS

Abstract

Mammalian sperm capacitation, defined as an obligatory maturational process leading to the development of the fertilization-competent state, results from a poorly understood series of morphological and molecular events. We report here that ejaculated bovine sperm, incubated under conditions that support capacitation in vitro, display a reproducible pattern of protein tyrosine phosphorylations that are regulated by a cAMP-dependent pathway. The appearance of these tyrosine phosphorylated proteins correlated temporally with the time course of capacitation induced by heparin, and these phosphorylations displayed a similar heparin concentration dependence. Glucose, which inhibits capacitation, inhibited these protein tyrosine phosphorylations in media containing heparin. The biologically active cAMP analogues (dibutyryl cAMP [db-cAMP], 8-bromo cAMP, sp-cAMPS) and the phosphodiesterase inhibitor 3-isobutyl-1-methylxanthine (IBMX) induced the same protein tyrosine phosphorylation patterns as seen with heparin. Moreover, these cAMP agonists could overcome the inhibition of the heparin-induced tyrosine phosphorylations by glucose. In contrast, Rp-adenosine-3',5'-cyclic monophosphorothioate (Rp-cAMPS), a protein kinase A (PK-A) antagonist, blocked the capacitation-associated increases in protein tyrosine phosphorylation. This cAMP regulation of the protein tyrosine phosphorylation pattern is mediated by PK-A since N-[2-(p-bromocinnamylamino) ethyl]-5-isoquinolinesulfonamide-dihydrochloride (H89), another inhibitor of PK-A, inhibited the heparin-induced protein tyrosine phosphorylation pattern in a concentration-dependent manner in either the absence or presence of db-cAMP, IBMX, and glucose. These data support a model for sperm capacitation that includes protein tyrosine phosphorylation as an important regulatory pathway, and a role for cAMP/PK-A in the regulation of this pathway leading to capacitation. These studies are the first to report a unique interrelationship between tyrosine kinase/phosphatase and cAMP signaling pathways at the level of PK-A in bovine sperm capacitation.

MeSH Terms
1-Methyl-3-isobutylxanthine/pharmacology Acrosome/physiology Animals Blotting, Western Cattle Culture Media Cyclic AMP/physiology Cyclic AMP-Dependent Protein Kinases/antagonists & inhibitors Electrophoresis, Polyacrylamide Gel Enzyme Inhibitors/pharmacology Glucose/pharmacology Heparin/pharmacology In Vitro Techniques Isoquinolines/pharmacology Male Phosphodiesterase Inhibitors/pharmacology Phosphorylation Protein Tyrosine Phosphatases/metabolism Sperm Capacitation/physiology Sulfonamides
Chemicals
Culture Media Enzyme Inhibitors Isoquinolines Phosphodiesterase Inhibitors Sulfonamides Heparin Cyclic AMP Cyclic AMP-Dependent Protein Kinases Protein Tyrosine Phosphatases Glucose N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide 1-Methyl-3-isobutylxanthine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Galantino-Homer H L
Center for Research on Reproduction and Women's Health, University of Pennsylvania School of Medicine, Philadelphia 19104-6080, USA.
Visconti P E
Kopf G S
Article Info
Journal
Biology of reproduction
Abbr.
Biol Reprod
ISSN
0006-3363
Published
1997-03-00
Pages
707-19
Language
English
Region
United States
NLM ID
0207224
Subset
IM
Grants
NIGMS NIH HHS · 5-T32-GM07170 · United States
NICHD NIH HHS · HD-06274 · United States
NICHD NIH HHS · HD-22732 · United States
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