References
-
J. Reprod. Fertil.
v.101
Regluation of flagellar motility of fowel spermatozoa: Evidence for the involvement of intracellular
$Ca^{2+}$ and calmodulin Ashizawa,K.;H.Tomonaga;Y.Tsuzuki https://doi.org/10.1530/jrf.0.1010265 - J. Reprod. Fertil. v.104 Regulatory mechanisms of fowel sperm motility: Possible role of endogenous myosin light chain kinase-like protein Ashizawa,K.;G.R.Wishart;Y.Tsuzuki https://doi.org/10.1530/jrf.0.1040141
-
Proc. Natl. Acad. Sci. USA
v.89
Early persistent activation of sperm
$K^+$ channels by the egg peptide speract Babcock,D.F.;M.Mosma;D.E.Battaglia;A.Darszon https://doi.org/10.1073/pnas.89.13.6001 - J. Fish Biol. v.19 Rainbow trout, Salmo gairdneri Richardson, spermatozoa: Effects of cations and pH on motility Baynes,S.M.;A.P.Scott;A.P.Dawson https://doi.org/10.1111/j.1095-8649.1981.tb05830.x
- J. Cell Sci. v.98 Membrane hyperpolarization activates trout sperm without an increase in intracellular pH Boitano,S.;C.K.Omoto
-
Cell Motil. Cytoskel.
v.21
Trout sperm swimming patterns and role of intracellilar
$Ca^{2+}$ Boitano,S.;C.K.Omoto https://doi.org/10.1002/cm.970210109 - J. Cell Biol. v.111 Purification of sea urchin sperm adenylyl cylase Bookbinder,H.;G.W.Moy;V.D.Vacquier https://doi.org/10.1083/jcb.111.5.1859
- Anal. Biochem. v.72 A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding Bradford,M.M. https://doi.org/10.1016/0003-2697(76)90527-3
- Cell Motil. Cytoskel. v.18 Calcium sensors in sea urchin sperm flagella Brokaw,C.J. https://doi.org/10.1002/cm.970180207
- J. Cell Biol. v.100 Modulation of the asymmetry of sea urchin sperm flagellar bending by calmodulin Brokaw,C.J.;S.M.Nagayama https://doi.org/10.1083/jcb.100.6.1875
-
J. Biol. Chem.
v.268
Selective modulation by cGMP of the
$K^{+}$ channel activated by speract Cook,S.P.;D.F.Babcock -
J. Biol. Chem.
v.268
Activation of
$Ca^{2+}$ permeability by cAMP is coordinated through the pH increase induced by speract Cook,S.P.;D.F.Babcock -
Cell Motil. Cytoskel.
v.14
Rise of internal
$Ca^{2+}$ accompanies the initiation of trout sperm motility Cosson,M.P.;R.Billard;L.Letellier https://doi.org/10.1002/cm.970140312 -
FEBS Lett.
v.372
Mouse sperm membrane potential: Changes induced by
$Ca^{2+}$ Espinosa,F.;A.Darszon https://doi.org/10.1016/0014-5793(95)00962-9 -
Dev. Biol.
v.221
Participation of a
$K^{+}$ channel modulation directly by cGMP in the speract-induced signaling cascade of Strongylocentrout purpuratus sea urchin sperm Galindo,B.E.;C.Beltran;E.J.Cragoe;A.Darszon https://doi.org/10.1006/dbio.2000.9678 - Annu. Rev. Biochem. v.58 Molecular basis of fertilization Garbers,D.L. https://doi.org/10.1146/annurev.bi.58.070189.003443
- FEBS Lett. v.218 A first transient hyperpolarization occurs during the sea urchin sperm acrosome reaction induced by egg jelly Gonzalez-Martinez,M.T.;A.Darszon https://doi.org/10.1016/0014-5793(87)81055-4
- J. Biol. Chem. v.256 Sodium-dependent activation of sea urchin spermatozoa by speract and monesin Hansbrough,J.R.;D.L.Garbers
- J. Biol. Chem. v.262 Involvement of tyrosine kinase in the initiation of flagellar movement in rainbow trout spermatozoa Hayashi,H.;K.Yamamoto;H.Yonekawa;M.Morisawa
- J. Cell Sci. v.111 Proteasomes regulate the motility of salmonid fish sperm through modulation of cAMP-dependent phosphorylation of an outer arm dynein light chain Inaba,K.;S.Morisawa;M.Morisawa
- Zool. Sci. v.4 Effects of calmodulin antagoists on motility and acrosome reaction of sea urchin sperm Iwasa,F.;Y.Hasegawa;H.Mohri
- Dev. Biol. v.213 Membrane hyperpolarization by sperm activating and attraction factor increase cAMP level and activate sperm motility in the ascidian Ciona intestinalis Izumi,H.;K.Inaba;Y.Oka;M.Morisawa https://doi.org/10.1006/dbio.1999.9367
- J. Microbiol. Biotechnol. v.13 Membrane hyperpolarization increases cAMP to induce the initiation of sperm motility in salmonid fishes Koh,K.H.;M.Morisawa;K.S.Chol
-
FEBS Lett.
v.388
T-type
$Ca^{2+}$ -channels and expression in spermatogenic cells, and their possibility relevance to the sperm acrosome reaction Lievano,A.;C.M.Santi;A.Darszon https://doi.org/10.1016/0014-5793(96)00515-7 - Cell v.13 A camp-induced increase in the mobility of demembraned bull sperm models Lindemann,C.B. https://doi.org/10.1016/0092-8674(78)90133-2
-
Ann, NY. Acad. Sci.
v.383
Regulation of the cytoskelton by
$Ca^{2+}$ -calmodulin and cAMP Means,A.R.;J.S.Tash;V.Guerriero https://doi.org/10.1111/j.1749-6632.1982.tb23162.x - Zool. Sci. v.11 Cell signaling mechanisms for sperm mobility Morisawa,M.
- Zool. Sci. v.2 Initiation mechanism of sperm motility at spawning in teleosts Morisawa,M.
- J. Exp. Zool. v.242 Short-term changes in levels of cyclic AMP, adenylatecyclase, and phosphodiesterase during the initiation of sperm motility in rainbow trout Morisawa,M.;K.Ishida https://doi.org/10.1002/jez.1402420211
- Zool. Sci. v.1 Initiation of sperm motility in Ciona intestinalis by calcium and cyclic AMP Morisawa,M.;S.Morisawa;R.D.Santis
- Nature v.295 Cyclic AMP induces maturation of trout sperm axoneme to initiate motility Morisawa,M.;M.Okuno https://doi.org/10.1038/295703a0
- Science v.210 Osmolarity and potassium ion: Their roles in initiation of sperm motility in teleosts Morisawa,M.;K.Suzuki https://doi.org/10.1126/science.7444445
- Biochem. Biophys. Res. Com. v.56 The activation of motility in quiescent hamster sperm from the epididymis by calcium and cyclic nucleotides Morton,B.;J.Hrrigan-Lum;L.Albabli;T.Jooss https://doi.org/10.1016/0006-291X(74)90852-3
- Dissertation. Life Science Institute, Graduate School of Science Nomura,M.
- Dev. Growth Differ. v.42 Cyclic AMP and calmodulin-dependent phosphorylation of 21 and 26 kDa proteins in axoneme is a prerequisite for SAAF-induced motile activation in ascidian spermatozoa Nomura,M.;K.Inaba;M.Morisawa https://doi.org/10.1046/j.1440-169x.2000.00489.x
- J. Biol. Chem. v.260 Sodium bicarbonate in seminal plasma stimulates the mobility of mammalian spermatozoa through direct activation of adenylyl cyclase Okamura,N.;Y.Tajima;Y.Sugita
- Cell Motil. Cytoskel. v.14 Effect of calcium on motility of rainbow trout sperm flagella demembraned with Triton X-100 Okuno,M.;M.Morisawa https://doi.org/10.1002/cm.970140206
-
Am. J. Physiol.
v.271
A dihydropyridine-sensitive T-type
$Ca^{2+}$ current is the main$Ca^{2+}$ current carrier in mouse primary spermatocytes Santi,C.M.;A.Darszon;A.Hernandez https://doi.org/10.1152/ajpcell.1996.271.5.C1583 - Zool. Sci. v.12 Structure, function and biosynthesis of sperm-activating peptides and fucose sulfate glycoconjugate in the extracellular coat of sea urchin eggs Suzuki,N. https://doi.org/10.2108/zsj.12.13
- Biol. Reprod. v.30 Stimulation of sperm respiration rates by speract and resact at alkaline extracelluar pH Suzuki,N.;D.L.Garbers https://doi.org/10.1095/biolreprod30.5.1167
- Mol. Reprod. Dev. v.39 Implication that potassium flux and increase in intracellular calcium are necessary for the initiation of sperm motility in salmonid fishes Tanimoto,S.;Y.Kudo;T.Nakazawa;M.Morisawa https://doi.org/10.1002/mrd.1080390409
- Dev. Growth Diff. v.30 Roles of potassium and calcium channels in the initiation of sperm motility in rainbow trout Tanimoto,S.;M.Morisawa https://doi.org/10.1111/j.1440-169X.1988.00117.x
- J. Cell Biol. v.106 Identification, characterization, and functional correlation of calmodulin-dependent protein phosphatase in sperm Tash,J.S.;M.Krinks;R.L.Means;A.R.Means https://doi.org/10.1083/jcb.106.5.1625
- Biol. Reprod. v.28 Cyclic adenosine 3',5'-monophosphate, calcium and protein phosphorylation in flagellar motility Tash,J.S.;A.R.Means https://doi.org/10.1095/biolreprod28.1.75
- J. Cell Biol. v.101 Chemotaxis of Arbacia punctulata spermatozoa to resact, a peptide from egg jelly layer Ward,C.R.;C.J.Brokaw;D.L.Garbers;V.D.Vacquier https://doi.org/10.1083/jcb.101.6.2324
- Dev. Biol. v.158 Molecular events mediating sperm activation Ward,C.R.;G.S.Kopf https://doi.org/10.1006/dbio.1993.1165
- Dev. Growth Differ v.36 Calcium and cyclic AMP mediate sperm activation, but calcium alone contributes sperm chemotaxis in the ascidian, Ciona savignyi Yoshida,M.;K.Inaba;K.Ishida;M.Morisawa https://doi.org/10.1111/j.1440-169X.1994.00589.x
- Annu. Rev. Neurosci. v.15 Guanylyl cyclase-linked receptors Yuen,P.S.;D.L.Garbers https://doi.org/10.1146/annurev.ne.15.030192.001205