دورية أكاديمية

Mouse sperm membrane potential hyperpolarization is necessary and sufficient to prepare sperm for the acrosome reaction.

التفاصيل البيبلوغرافية
العنوان: Mouse sperm membrane potential hyperpolarization is necessary and sufficient to prepare sperm for the acrosome reaction.
المؤلفون: De La Vega-Beltran JL; Departamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos 62210, México., Sánchez-Cárdenas C, Krapf D, Hernandez-González EO, Wertheimer E, Treviño CL, Visconti PE, Darszon A
المصدر: The Journal of biological chemistry [J Biol Chem] 2012 Dec 28; Vol. 287 (53), pp. 44384-93. Date of Electronic Publication: 2012 Oct 24.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID: 2985121R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1083-351X (Electronic) Linking ISSN: 00219258 NLM ISO Abbreviation: J Biol Chem Subsets: MEDLINE
أسماء مطبوعة: Publication: 2021- : [New York, NY] : Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology
Original Publication: Baltimore, MD : American Society for Biochemistry and Molecular Biology
مواضيع طبية MeSH: Acrosome Reaction*, Spermatozoa/*physiology, Animals ; Cell Membrane/metabolism ; Cell Polarity ; Female ; Male ; Membrane Potentials ; Mice ; Phosphorylation
مستخلص: Mammalian sperm are unable to fertilize the egg immediately after ejaculation; they acquire this capacity during migration in the female reproductive tract. This maturational process is called capacitation and in mouse sperm it involves a plasma membrane reorganization, extensive changes in the state of protein phosphorylation, increases in intracellular pH (pH(i)) and Ca(2+) ([Ca(2+)](i)), and the appearance of hyperactivated motility. In addition, mouse sperm capacitation is associated with the hyperpolarization of the cell membrane potential. However, the functional role of this process is not known. In this work, to dissect the role of this membrane potential change, hyperpolarization was induced in noncapacitated sperm using either the ENaC inhibitor amiloride, the CFTR agonist genistein or the K(+) ionophore valinomycin. In this experimental setting, other capacitation-associated processes such as activation of a cAMP-dependent pathway and the consequent increase in protein tyrosine phosphorylation were not observed. However, hyperpolarization was sufficient to prepare sperm for the acrosome reaction induced either by depolarization with high K(+) or by addition of solubilized zona pellucida (sZP). Moreover, K(+) and sZP were also able to increase [Ca(2+)](i) in non-capacitated sperm treated with these hyperpolarizing agents but not in untreated cells. On the other hand, in conditions that support capacitation-associated processes blocking hyperpolarization by adding valinomycin and increasing K(+) concentrations inhibited the agonist-induced acrosome reaction as well as the increase in [Ca(2+)](i). Altogether, these results suggest that sperm hyperpolarization by itself is key to enabling mice sperm to undergo the acrosome reaction.
References: J Biol Chem. 2004 Aug 6;279(32):33742-50. (PMID: 15178683)
Physiology (Bethesda). 2010 Jun;25(3):165-75. (PMID: 20551230)
J Cell Physiol. 2007 Sep;212(3):753-63. (PMID: 17450521)
J Biol Chem. 2009 Dec 18;284(51):35495-506. (PMID: 19837660)
Proc Natl Acad Sci U S A. 2007 May 1;104(18):7688-92. (PMID: 17460039)
Hum Mol Genet. 2012 Mar 15;21(6):1287-98. (PMID: 22121115)
Proc Natl Acad Sci U S A. 2007 Jun 5;104(23):9816-21. (PMID: 17519339)
Biol Reprod. 2012 Jan 19;86(1):1-14. (PMID: 21976599)
Proc Natl Acad Sci U S A. 1999 Jun 8;96(12):6757-62. (PMID: 10359785)
Nature. 2011 Mar 17;471(7338):387-91. (PMID: 21412339)
FEBS Lett. 2010 Mar 5;584(5):1041-6. (PMID: 20138882)
Dev Cell. 2005 Aug;9(2):249-59. (PMID: 16054031)
Development. 1995 Apr;121(4):1129-37. (PMID: 7743926)
Biol Reprod. 2011 Jul;85(1):179-88. (PMID: 21471298)
Biol Reprod. 2009 Jan;80(1):115-23. (PMID: 18784352)
Dev Biol. 1992 Aug;152(2):304-14. (PMID: 1379559)
Nat Cell Biol. 2003 Dec;5(12):1117-22. (PMID: 14634667)
FEBS Lett. 1995 Sep 18;372(1):119-25. (PMID: 7556631)
Dev Biol. 2006 Jan 15;289(2):395-405. (PMID: 16343479)
J Biol Chem. 2011 Aug 26;286(34):30232-43. (PMID: 21737448)
FEBS Lett. 2001 Nov 30;509(1):119-25. (PMID: 11734218)
Proc Natl Acad Sci U S A. 2011 Apr 5;108(14):5879-84. (PMID: 21427226)
J Biol Chem. 1992 Jul 15;267(20):14061-7. (PMID: 1629205)
Physiol Rev. 2002 Jul;82(3):769-824. (PMID: 12087135)
J Biol Chem. 1999 Jan 29;274(5):3235-42. (PMID: 9915865)
FEBS Lett. 1998 Apr 10;426(1):47-51. (PMID: 9598976)
J Cell Physiol. 2013 Mar;228(3):590-601. (PMID: 22833409)
Biochem Biophys Res Commun. 2009 Apr 3;381(2):204-9. (PMID: 19338774)
Reprod Biol Endocrinol. 2009 Oct 27;7:119. (PMID: 19860887)
J Biol Chem. 2004 Jul 2;279(27):28220-6. (PMID: 15078889)
Mol Pharmacol. 1998 Jun;53(6):1104-11. (PMID: 9614215)
J Biol Chem. 2003 Feb 28;278(9):7001-9. (PMID: 12496293)
Proc Natl Acad Sci U S A. 2009 Jan 20;106(3):667-8. (PMID: 19144927)
Am J Physiol. 1996 Nov;271(5 Pt 1):C1583-93. (PMID: 8944642)
J Biol Chem. 2006 Mar 3;281(9):5623-33. (PMID: 16407190)
Br J Pharmacol. 2011 Nov;164(6):1684-97. (PMID: 21557738)
Biol Reprod. 2009 Jun;80(6):1092-8. (PMID: 19211808)
FEBS Lett. 1996 Jun 17;388(2-3):150-4. (PMID: 8690075)
Biol Reprod. 2010 Oct;83(4):507-13. (PMID: 20463353)
IUBMB Life. 2007 Apr-May;59(4-5):286-92. (PMID: 17505967)
Am J Physiol Lung Cell Mol Physiol. 2012 May 15;302(10):L1128-39. (PMID: 22387294)
Biol Reprod. 1998 Jul;59(1):12-6. (PMID: 9674987)
Development. 1995 Apr;121(4):1139-50. (PMID: 7538069)
Development. 1994 Nov;120(11):3313-23. (PMID: 7720569)
Asian J Androl. 2011 May;13(3):395-405. (PMID: 21540868)
Dev Biol. 1995 Oct;171(2):554-63. (PMID: 7556936)
Exp Cell Res. 2012 Mar 10;318(5):478-88. (PMID: 22248876)
J Biol Chem. 2010 Aug 20;285(34):26269-78. (PMID: 20551332)
Biotechniques. 2006 Aug;41(2):191-7. (PMID: 16925021)
J Cell Sci. 2012 Jan 15;125(Pt 2):473-85. (PMID: 22302997)
Biophys J. 2003 Jun;84(6):3508-28. (PMID: 12770864)
Cell Calcium. 2006 Aug;40(2):241-52. (PMID: 16797697)
Annu Rev Physiol. 2012;74:453-75. (PMID: 22017176)
J Membr Biol. 2009 Oct;231(2-3):65-78. (PMID: 19865788)
Dev Biol. 2001 Aug 1;236(1):210-9. (PMID: 11456455)
Physiol Rev. 2011 Oct;91(4):1305-55. (PMID: 22013213)
Dev Biol. 2001 Jun 1;234(1):261-74. (PMID: 11356034)
Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13004-9. (PMID: 8917534)
J Biol Chem. 2007 Aug 17;282(33):24397-406. (PMID: 17588945)
FEBS Lett. 2004 Apr 9;563(1-3):87-92. (PMID: 15063728)
معلومات مُعتمدة: R01 HD038082 United States HD NICHD NIH HHS; R01 HD044044 United States HD NICHD NIH HHS; HD038082 United States HD NICHD NIH HHS; R01 HD44044 United States HD NICHD NIH HHS
تواريخ الأحداث: Date Created: 20121026 Date Completed: 20130325 Latest Revision: 20211021
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC3531752
DOI: 10.1074/jbc.M112.393488
PMID: 23095755
قاعدة البيانات: MEDLINE
الوصف
تدمد:1083-351X
DOI:10.1074/jbc.M112.393488