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PMID: 8020107 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Role of cAMP in the reactivation of demembranated ram spermatozoa.

Cell motility and the cytoskeleton ·Vol. 27 ·No. 3 ·1994-00-00 ·Pages 206-18

San Agustin JT, Witman GB

Abstract

Ejaculated ram sperm were demembranated with Triton X-100, separated from the detergent-soluble matrix, and reactivated [San Agustin and Witman (1993): Cell Motil. Cytoskeleton 24:264-273]. The percent motility of models prepared from freshly washed sperm was comparable to that of the washed sample before demembranation, regardless of whether cAMP was included in the reactivation medium. However, demembranated models derived from aging or metabolically inhibited sperm exhibited a lower percent reactivation and required cAMP to attain the level of motility of freshly washed sperm. Cyclic AMP was approximately 100 times more effective than cGMP. The requirement for cAMP could be bypassed by addition of porcine heart cAMP-dependent protein kinase (PKA) catalytic subunit to the reactivation medium, demonstrating that cAMP was acting via PKA. The cAMP stimulation of reactivation was not affected by inclusion of the PKA inhibitor PKI(5-24) in the reactivation medium, but was decreased when the models were preincubated with PKI(5-24) prior to reactivation. The cytosol-free models retained > 90% of the sperm PKA activity; therefore, the PKA appears to be anchored to internal sperm structures. This PKA could not be extracted by cAMP or Triton X-100 alone, but only by cAMP and Triton X-100 in combination. We conclude that cAMP-dependent protein phosphorylation is critical for sperm motility, but that the essential protein phosphate sites turn over slowly under our reactivation conditions, so that the cAMP requirement is apparent only in models prepared from sperm having a low internal ATP or cAMP content. Interestingly, reactivation was rapidly blocked by the peptide arg-lys-arg-ala-arg-lys-glu, which has been reported to be a selective inhibitor of cGMP-dependent protein kinase.

MeSH Terms
Adenosine Triphosphate/metabolism Amino Acid Sequence Animals Cell Membrane/drug effects Cyclic AMP/pharmacology,physiology Cyclic AMP-Dependent Protein Kinases/isolation & purification,physiology Cyclic GMP/pharmacology Male Molecular Sequence Data Octoxynol/pharmacology Oligopeptides/pharmacology Peptide Fragments/pharmacology Phosphorylation Protease Inhibitors/pharmacology Protein Processing, Post-Translational Sheep Sperm Motility/physiology Spermatozoa/drug effects,physiology,ultrastructure
Chemicals
Oligopeptides Peptide Fragments Protease Inhibitors protein kinase inhibitor peptide (5-24) arginyl-lysyl-arginyl-alanyl-arginyl-lysyl-glutamic acid Adenosine Triphosphate Octoxynol Cyclic AMP Cyclic AMP-Dependent Protein Kinases Cyclic GMP
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
San Agustin J T
Male Fertility Program, Worcester Foundation for Experimental Biology, Shrewsbury, MA 01545.
Witman G B
Article Info
Journal
Cell motility and the cytoskeleton
Abbr.
Cell Motil Cytoskeleton
ISSN
0886-1544
Published
1994-00-00
Pages
206-18
Language
English
Region
United States
NLM ID
8605339
Subset
IM
Grants
NICHD NIH HHS · HD 23858 · United States
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