Sperm activation: Role of reactive oxygen species and kinases

被引:224
作者
de lamirande, Eve [1 ,2 ]
O'Flaherty, Cristian [3 ]
机构
[1] Royal Victoria Hosp, Urol Res Lab, Montreal, PQ H3A 1A1, Canada
[2] McGill Univ, Montreal, PQ H3A 1A1, Canada
[3] McGill Univ, Fac Med, Dept Pharmacol & Therapeut, Montreal, PQ H3G 1Y6, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2008年 / 1784卷 / 01期
基金
加拿大健康研究院;
关键词
spermatozoa; capacitation; reactive oxygen species; protein phosphorylation; signal transduction;
D O I
10.1016/j.bbapap.2007.08.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Reactive oxygen species (ROS), such as the superoxide anion (02 and controlled levels, act as second messengers. ROS regulate sperm capacitation, which is the complex series of changes allowing spermatozoa to bind to the zona pellucida surrounding the oocyte, induce the acrosome reaction (exocytotic event by which proteolytic enzymes are released) and fertilize the oocyte. Capacitating spermatozoa produce controlled amounts of ROS that regulate downstream events: first, the increase in cAMP, protein kinase A (PKA) activation and phosphorylation of PKA substrates (arginine-X-X-serine/threonine motif; 15-30 min); second, the phosphorylation of MEK (extracellular signal regulated kinase [ERK] kinase)-like proteins (30-60 min) and then that of the threonine-glutamate-tyrosine motif (>1 h); finally, the late tyrosine phosphorylation of fibrous sheath proteins (>2 h). Although all these events are ROS-dependent, the regulation by various kinases, protein kinase C, PKA, protein tyrosine kinases, the ERK pathway, etc. is different. ROS also regulate the acquisition of hyperactivated motility and the acrosome reaction by spermatozoa. ROS action is probably mediated via the sulfhydryl/disulfide pair on sperm proteins. Redundancy, cross talk, and multiple systems acting in parallel point to an array of safeguards assuring the timely function of spermatozoa. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:106 / 115
页数:10
相关论文
共 82 条
  • [1] Proteomic changes in mammalian spermatozoa during epididymal maturation
    Aitken, R. John
    Nixon, Brett
    Lin, Minjie
    Koppers, Adam J.
    Lee, Yun H.
    Baker, Mark A.
    [J]. ASIAN JOURNAL OF ANDROLOGY, 2007, 9 (04) : 554 - 564
  • [2] Aitken RJ, 1998, J CELL SCI, V111, P645
  • [3] A FREE-RADICAL THEORY OF MALE-INFERTILITY
    AITKEN, RJ
    [J]. REPRODUCTION FERTILITY AND DEVELOPMENT, 1994, 6 (01) : 19 - 24
  • [4] [Anonymous], [No title captured]
  • [5] Use of phosphoproteomics to study tyrosine kinase activity in capacitating boar sperm Kinase activity and capacitation
    Bailey, JL
    Tardif, S
    Dubé, C
    Beaulieu, M
    Reyes-Moreno, C
    Lefièvre, L
    Leclerc, P
    [J]. THERIOGENOLOGY, 2005, 63 (02) : 599 - 614
  • [6] A multi-centre cohort study of the physical health of 5-year-old children conceived after intracytoplasmic sperm injection, in vitro fertilization and natural conception
    Bonduelle, M
    Wennerholm, UB
    Loft, A
    Tarlatzis, BC
    Peters, C
    Henriet, S
    Mau, C
    Victorin-Cederquist, A
    Van Steirteghem, A
    Balaska, A
    Emberson, JR
    Sutcliffe, AG
    [J]. HUMAN REPRODUCTION, 2005, 20 (02) : 413 - 419
  • [7] Regulation of protein tyrosine phosphorylation in human sperm by a calcium/calmodulin-dependent mechanism: Identification of a kinase anchor proteins as major substrates for tyrosine phosphorylation
    Carrera, A
    Moos, J
    Ning, XP
    Gerton, GL
    Tesarik, J
    Kopf, GS
    Moss, SB
    [J]. DEVELOPMENTAL BIOLOGY, 1996, 180 (01) : 284 - 296
  • [8] Free radical-induced liquefaction of ejaculated human semen: A new dimension in semen biochemistry
    Chatterjee, S
    Laloraya, M
    Kumar, PG
    [J]. ARCHIVES OF ANDROLOGY, 1997, 38 (02): : 107 - 111
  • [9] Biological basis for human capacitation
    De Jonge, C
    [J]. HUMAN REPRODUCTION UPDATE, 2005, 11 (03) : 205 - 214
  • [10] de Lamirande E, 1998, J ANDROL, V19, P585