The association between CDC42 and caveolin-1 is involved in the regulation of capacitation and acrosome reaction of guinea pig and mouse sperm

Reproduction

Volumn 144, Issue 1, 2012, Pages 123-134

  Baltierrez Hoyos R ^a   Roa Espitia, A L ^a   Hernandez Gonzalez E O ^a  

^a DEPARTAMENTO DE FÍSICA   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM ION; CAVEOLIN 1; GUANINE NUCLEOTIDE DISSOCIATION INHIBITOR; PROGESTERONE; PROTEIN CDC42; RHO FACTOR; SNARE PROTEIN; TYROSINE;

ACROSOME REACTION; ACTIN POLYMERIZATION; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; EXOCYTOSIS; GUINEA PIG; IMMUNOPRECIPITATION; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; SPERMATOZOON CAPACITATION;

ACROSOME; ACROSOME REACTION; ANIMALS; BENZAZEPINES; CAVEOLIN 1; CDC42 GTP-BINDING PROTEIN; CELL MEMBRANE; GUINEA PIGS; HOMEOSTASIS; IMMUNOSORBENT TECHNIQUES; MALE; MICE; OXIMES; PHOSPHORYLATION; PROGESTERONE; SIGNAL TRANSDUCTION; SPERM CAPACITATION; SPERMATOZOA;

CAVIA; MAMMALIA;

EID: 84863205283     PISSN: 14701626     EISSN: 17417899     Source Type: Journal    
DOI: 10.1530/REP-11-0433     Document Type: Article

References (56)

1. Baker MA, Hetherington L & Aitken RJ 2006 Identification of SRC as a key PKA-stimulated tyrosine kinase involved in the capacitation-associated hyperactivation of murine spermatozoa. Journal of Cell Science 119 3182-3192. (doi:10.1242/jcs.03055)
2. Banquet S, Delannoy E, Agouni A, Dessy C, Lacomme S, Hubert F, Richard V, Muller B & Leblais V 2011 Role of G(i/o)-Src kinase-PI3K/Akt pathway and caveolin-1 in beta-adrenoceptor coupling to endothelial NO synthase in mouse pulmonary artery. Cellular Signalling 23 1136-1143. (doi:10.1016/j.cellsig.2011. 02.008)
3. Bastian Y, Roa-Espitia AL, Mujica A & Hernandez-Gonzalez EO 2010 Calpain modulates capacitation and acrosome reaction through cleavage of the spectrin cytoskeleton. Reproduction 140 673-684. (doi:10.1530/REP-09-0545)
4. Belmonte SA, Lopez CI, Roggero CM, De Blas GA, Tomes CN & Mayorga LS 2005 Cholesterol content regulates acrosomal exocytosis by enhancing Rab3A plasma membrane association. Developmental Biology 285 393-408. (doi:10.1016/j.ydbio.2005.07.001)
5. Brener E, Rubinstein S, Cohen G, Shternall K, Rivlin J & Breitbart H 2003 Remodeling of the actin cytoskeleton during mammalian sperm capacitation and acrosome reaction. Biology of Reproduction 68 837-845. (doi:10.1095/ biolreprod.102.009233)
6. Buchsbaum RJ 2007 Rho activation at a glance. Journal of Cell Science 120 1149-1152. (doi:10.1242/jcs.03428)
7. Cabello-Agueros JF, Hernandez-Gonzalez EO & Mujica A 2003 The role of F-actin cytoskeleton-associated gelsolin in the guinea pig capacitation and acrosome reaction. Cell Motility and the Cytoskeleton 56 94-108. (doi:10.1002/cm.10135)
8. Cao H, Courchesne WE & Mastick CC 2002 A phosphotyrosine-dependent protein interaction screen reveals a role for phosphorylation of caveolin-1 on tyrosine 14: recruitment of C-terminal Src kinase. Journal of Biological Chemistry 277 8771-8774. (doi:10.1074/jbc.C100661200)
9. Cao H, Sanguinetti AR & Mastick CC 2004 Oxidative stress activates both Src-kinases and their negative regulator Csk and induces phosphorylation of two targeting proteins for Csk: caveolin-1 and paxillin. Experimental Cell Research 294 159-171. (doi:10.1016/j.yexcr.2003.11.010)
10. Cohen G, Rubinstein S, Gur Y & Breitbart H 2004 Crosstalk between protein kinase A and C regulates phospholipase D and F-actin formation during sperm capacitation. Developmental Biology 267 230-241. (doi:10.1016/j.ydbio. 2003.10.034)
11. 2+ fluctuations in sperm physiology. International Review of Cytology 243 79-172. (doi:10.1016/50074-7696(05)43002-8)
12. De Blas GA, Roggero CM, Tomes CN & Mayorga LS 2005 Dynamics of SNARE assembly and disassembly during sperm acrosomal exocytosis. PLoS Biology 3 e323. (doi:10.1371/journal.pbio.0030323)
13. Delgado-Buenrostro NL, Hernandez-Gonzalez EO, Segura-Nieto M & Mujica A 2005 Actin polymerization in the equatorial and postacrosomal regions of guinea pig spermatozoa during the acrosome reaction is regulated by G proteins. Molecular Reproduction and Development 70 198-210. (doi:10.1002/mrd.20192)
14. Ducummon CC & Berger T 2006 Localization of the Rho GTPases and some Rho effector proteins in the sperm of several mammalian species. Zygote 14 249-257. (doi:10.1017/S0967199406003790)
15. Gasman S, Chasserot-Golaz S, Malacombe M, Way M & Bader MF 2004 Regulated exocytosis in neuroendocrine cells: a role for subplasmalemmal Cdc42/N-WASP-induced actin filaments. Molecular Biology of the Cell 15 520-531. (doi:10.1091/mbc.E03-06-0402)
16. Goupil S, La Salle S, TraslerJM,Bordeleau LJ&Leclerc P 2011Developmental expression of SRC-related tyrosine kinases in the mouse testis. Journal of Andrology 32 95-110. (doi:10.2164/jandrol.110.010462)
17. Grande-Garcia A & del Pozo MA 2008 Caveolin-1 in cell polarization and directional migration. European Journal of Cell Biology 87 641-647. (doi:10.1016/j.ejcb.2008.02.001)
18. Head BP & Insel PA 2007 Do caveolins regulate cells by actions outside of caveolae? Trends in Cell Biology 17 51-57. (doi:10.1016/j.tcb.2006. 11.008)
19. Hernandez-Gonzalez EO, Lecona-Valera AN, Escobar-Herrera J & Mujica A 2000 Involvement of an F-actin skeleton on the acrosome reaction in guinea pig spermatozoa. Cell Motility and the Cytoskeleton 46 43-58. (doi:10.1002/(SICI) 1097-0169(200005)46:1<43::AID-CM5>3.0.CO;2-1)
20. Hong-Geller E & Cerione RA 2000 Cdc42 and Rac stimulate exocytosis of secretory granules by activating the IP(3)/calcium pathway in RBL-2H3 mast cells. Journal of Cell Biology 148 481-494. (doi:10.1083/jcb.148.3.481)
21. Kierszenbaum AL, Rivkin E, Talmor-Cohen A, Shalgi R & Tres LL 2009 Expression of full-length and truncated Fyn tyrosine kinase transcripts and encoded proteins during spermatogenesis and localization during acrosome biogenesis and fertilization. Molecular Reproduction and Development 76 832-843. (doi:10.1002/mrd.21049)
22. Krapf D, Arcelay E, Wertheimer EV, Sanjay A, Pilder SH, Salicioni AM & Visconti PE 2010 Inhibition of Ser/Thr phosphatases induces capacitation-associated signaling in the presence of Src kinase inhibitors. Journal of Biological Chemistry 285 7977-7985. (doi:10.1074/jbc.M109.085845)
23. Leclerc P & Goupil S 2002 Regulation of the human sperm tyrosine kinase c-yes. Activation by cyclic adenosine 3′,5′-monophosphate and inhibition by Ca(2+). Biology of Reproduction 67 301-307. (doi:10.1095/ biolreprod67.1.301)
24. Lee H, Volonte D, Galbiati F, Iyengar P, Lublin DM, Bregman DB, Wilson MT, Campos-Gonzalez R, Bouzahzah B, Pestell RG et al. 2000 Constitutive and growth factor-regulated phosphorylation of caveolin-1 occurs at the same site (Tyr-14) in vivo: identification of a c-Src/ Cav-1/Grb7 signaling cassette. Molecular Endocrinology 14 1750-1775. (doi:10.1210/me.14.11.1750)
25. Malacombe M, Ceridono M, Calco V, Chasserot-Golaz S, McPherson PS, Bader MF & Gasman S 2006 Intersectin-1L nucleotide exchange factor regulates secretory granule exocytosis by activating Cdc42. EMBO Journal 25 3494-3503. (doi:10.1038/sj.emboj.7601247)
26. Markwell MA, Haas SM, Bieber LL & Tolbert NE 1978 A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples. Analytical Biochemistry 87 206-210. (doi:10.1016/0003- 2697(78)90586-9)
27. Mayorga LS, Tomes CN & Belmonte SA 2007 Acrosomal exocytosis, a special type of regulated secretion. IUBMB Life 59 286-292. (doi:10.1080/ 15216540701222872)
28. Miranda PV, Allaire A, Sosnik J & Visconti PE 2009 Localization of low-density detergent-resistant membrane proteins in intact and acrosome-reacted mouse sperm. Biology of Reproduction 80 897-904. (doi:10.1095/biolreprod.108. 075242)
29. Mitchell LA, Nixon B, Baker MA & Aitken RJ 2008 Investigation of the role of SRC in capacitation-associated tyrosine phosphorylation of human spermatozoa. Molecular Human Reproduction 14 235-243. (doi:10.1093/molehr/ gan007)
30. Momboisse F, Ory S, Ceridono M, Calco V, Vitale N, Bader MF & Gasman S 2010 The Rho guanine nucleotide exchange factors Intersectin 1L and beta-Pix control calcium-regulated exocytosis in neuroendocrine PC12 cells. Cellular and Molecular Neurobiology 30 1327-1333. (doi:10.1007/s10571-010-9580-2)
31. Moore GD, Ayabe T, Visconti PE, Schultz RM & Kopf GS 1994 Roles of heterotrimeric and monomeric G proteins in sperm-induced activation of mouse eggs. Development 120 3313-3323. (Pubitemid 24343261)
32. Mullins RD 2000 How WASP-family proteins and the Arp2/3 complex convert intracellular signals into cytoskeletal structures. Current Opinion in Cell Biology 12 91-96. (doi:10.1016/S0955-0674(99)00061-7)
33. Muriel O, Echarri A, Hellriegel C, Pavon DM, Beccari L & Del Pozo MA 2011 Phosphorylated filamin A regulates actin-linked caveolae dynamics. Journal of Cell Science 124 2763-2776. (doi:10.1242/jcs.080804)
34. Nevins AK & Thurmond DC 2003 Glucose regulates the cortical actin network through modulation of Cdc42 cycling to stimulate insulin secretion. American Journal of Physiology Cell Physiology 285 C698-C710. (doi:10.1152/ajpcell.00093.2003)
35. Nevins AK & Thurmond DC 2005 A direct interaction between Cdc42 and vesicle-associated membrane protein 2 regulates SNARE-dependent insulin exocytosis. Journal of Biological Chemistry 280 1944-1952. (doi:10.1074/jbc. M409528200)
36. Nevins AK & Thurmond DC 2006 Caveolin-1 functions as a novel Cdc42 guanine nucleotide dissociation inhibitor in pancreatic beta-cells. Journal of Biological Chemistry 281 18961-18972. (doi:10.1074/jbc.M603604200)
37. Park DS, Cohen AW, Frank PG, Razani B, Lee H,Williams TM, Chandra M, Shirani J, De Souza AP, Tang B et al. 2003 Caveolin-1 null (-/-) mice show dramatic reductions in life span. Biochemistry 42 15124-15131. (doi:10.1021/bi0356348)
38. Parton RG, Hanzal-Bayer M & Hancock JF 2006 Biogenesis of caveolae: a structural model for caveolin-induced domain formation. Journal of Cell Science 119 787-796. (doi:10.1242/jcs.02853)
39. Pelish HE, Peterson JR, Salvarezza SB, Rodriguez-Boulan E, Chen JL, StamnesM,Macia E, Feng Y, Shair MD & Kirchhausen T 2006 Secramine inhibits Cdc42-dependent functions in cells and Cdc42 activation in vitro. Nature Chemical Biology 2 39-46. (doi:10.1038/nchembio751)
40. Peterson JR, Lebensohn AM, Pelish HE & Kirschner MW 2006 Biochemical suppression of small-molecule inhibitors: a strategy to identify inhibitor targets and signaling pathway components. Chemistry & Biology 13 443-452. (doi:10.1016/j.chembiol.2006.02.009)
41. Post H, Schwarz A, Brandenburger T, Aumuller G & Wilhelm B 2010 Arrangement of PMCA4 in bovine sperm membrane fractions. International Journal of Andrology 33 775-783. (doi:10.1111/j.1365-2605.2009.01022.x)
42. Razani B, Engelman JA, Wang XB, Schubert W, Zhang XL, Marks CB, Macaluso F, Russell RG, Li M, Pestell RG et al. 2001 Caveolin-1 null mice are viable but show evidence of hyperproliferative and vascular abnormalities. Journal of Biological Chemistry 276 38121-38138. (doi:10.1074/jbc.M008340200)
43. Razani B, Combs TP, Wang XB, Frank PG, Park DS, Russell RG, Li M, Tang B, Jelicks LA, Scherer PE et al. 2002 Caveolin-1-deficient mice are lean, resistant to diet-induced obesity, and show hypertriglyceridemia with adipocyte abnormalities. Journal of Biological Chemistry 277 8635-8647. (doi:10.1074/jbc.M110970200)
44. Rogers BJ, Bastias C, Coulson RL & Russell LD 1989 Cytochalasin D inhibits penetration of hamster eggs by guinea pig and human spermatozoa. Journal of Andrology 10 275-282. (Pubitemid 19206761)
45. Salicioni AM, Platt MD, Wertheimer EV, Arcelay E, Allaire A, Sosnik J & Visconti PE 2007 Signalling pathways involved in sperm capacitation. Society of Reproduction and Fertility Supplement 65 245-259.
46. Sanchez-Gutierrez M, Contreras RG & Mujica A 2002 Cytochalasin-D retards sperm incorporation deep into the egg cytoplasm but not membrane fusion with the egg plasma membrane. Molecular Reproduction and Development 63 518-528. (doi:10.1002/mrd.10203)
47. Shoeb M, Laloraya M & Kumar PG 2010 Progesterone-induced reorganisation of NOX-2 components in membrane rafts is critical for sperm functioning in Capra hircus. Andrologia 42 356-365. (doi:10.1111/j.1439-0272. 2009.01024.x)
48. Sleight SB, Miranda PV, Plaskett NW, Maier B, Lysiak J, Scrable H, Herr JC & Visconti PE 2005 Isolation and proteomic analysis of mouse sperm detergent-resistant membrane fractions: evidence for dissociation of lipid rafts during capacitation. Biology of Reproduction 73 721-729. (doi:10.1095/ biolreprod.105.041533)
49. Song KS, Scherer PE, Tang Z,Okamoto T, Li S, Chafel M, Chu C, Kohtz DS & Lisanti MP 1996 Expression of caveolin-3 in skeletal, cardiac, and smooth muscle cells. Caveolin-3 is a component of the sarcolemma and co-fractionates with dystrophin and dystrophin-associated glycoproteins. Journal of Biological Chemistry 271 15160-15165. (doi:10.1074/jbc.271.25.15160)
50. Sousa AP, Gomes-Santos CS & Ramalho-Santos J 2006 Localization of SNAREs, NSF and Caveolin 1 in human spermatozoa: relationship with seminal parameters. Archives of Andrology 52 347-353. (doi:10.1080/01485010600667050)
51. Stahlhut M & van Deurs B 2000 Identification of filamin as a novel ligand for caveolin-1: evidence for the organization of caveolin-1-associated membrane domains by the actin cytoskeleton. Molecular Biology of the Cell 11 325-337. (Pubitemid 30075526)
52. Tapia S, Rojas M, Morales P, Ramirez MA & Diaz ES 2011 The laminin-induced acrosome reaction in human sperm is mediated by Src kinases and the proteasome. Biology of Reproduction 85 357-366. (doi:10.1095/biolreprod.111. 092254)
53. Trifaro JM, Gasman S & Gutierrez LM 2008 Cytoskeletal control of vesicle transport and exocytosis in chromaffin cells. Acta Physiologica 192 165-172. (doi:10.1111/j.1748-1716.2007.01808.x)
54. Tsai PS, De Vries KJ, De Boer-Brouwer M, Garcia-Gil N, Van Gestel RA, Colenbrander B, Gadella BM & Van Haeften T 2007 Syntaxin and VAMP association with lipid rafts depends on cholesterol depletion in capacitating sperm cells. Molecular Membrane Biology 24 313-324. (doi:10.1080/ 09687860701228692)
55. Ushio-Fukai M, Hilenski L, Santanam N, Becker PL, Ma Y, Griendling KK & Alexander RW 2001 Cholesterol depletion inhibits epidermal growth factor receptor transactivation by angiotensin II in vascular smooth muscle cells: role of cholesterol-rich microdomains and focal adhesions in angiotensin II signaling. Journal of Biological Chemistry 276 48269-48275. (doi:10.1074/jbc. M105901200)
56. Witte TS & Schafer-Somi S 2007 Involvement of cholesterol, calcium and progesterone in the induction of capacitation and acrosome reaction of mammalian spermatozoa. Animal Reproduction Science 102 181-193. (doi:10.1016/j.anireprosci.2007.07.007)