Inhibition of human sperm function and mouse fertilization in vitro by an antibody against cation channel of sperm 1: the contraceptive potential of its transmembrane domains and pore region

被引:42
作者
Li, Honggang [1 ]
Ding, Xiaofang [2 ]
Guan, Huangtao [1 ]
Xiong, Chengliang [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Family Planning Res Inst, Wuhan 430030, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Ctr Reprod Med, Wuhan 430030, Peoples R China
关键词
Immunocontraception; CatSper1; sperm; ion channel; EATON-MYASTHENIC-SYNDROME; MALE-FERTILITY; ION CHANNELS; SPERMATOZOA; MOTILITY; IMMUNOCONTRACEPTION; EXPRESSION; CATSPER1; TARGETS; TESTIS;
D O I
10.1016/j.fertnstert.2008.07.1751
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
Objective: To explore the contraceptive potential of the CatSper1 transmembrane domains and pore region in vitro. Design: In vitro study with human sperm and mouse fertilization. Setting: Andrology laboratory of an academic research center. Patient(s) and Animal(s): Normozoospermia and viripotent BALB/c mice. Intervention(s): The specific binding of an anti-CatSper1 IgG antibody (H-300) to CatSper1 was confirmed by Western blot and immunofluorescence. Sperm from humans and mice were incubated with H-300. Main Outcome Measure(s): The effects of H-300 on human sperm progressive motility, abnormal acrosome, hyperactivated motility, and mouse in vitro fertilization rates were analyzed. Result(s): A significant decline in sperm progressive motility was observed after 1, 2, and 4 hours of incubation with H-300; the change was mainly ascribed to the decline of fast progressive motility. Significant inhibition of the hyperactivated motility was observed after 5 hours of incubation with H-300. The incubation of mouse sperm with H-300 before insemination reduced the in vitro fertilization rate to 28% of control levels (72% inhibition). Conclusion(s): CatSper1 may be a potential target for immunocontraception, and the antibody may be a tool to study the function of ion channels in sperm in which relatively fewer methods can be applied. (Fertil Steril (R) 2009;92:1141-6. (C)2009 by American Society for Reproductive Medicine.)
引用
收藏
页码:1141 / 1146
页数:6
相关论文
共 24 条
[1]
Immunocontraceptive vaccines for human use [J].
Aitken, RJ .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2002, 57 (1-2) :273-287
[2]
BRONSON R, 1984, FERTIL STERIL, V42, P171
[3]
CatSper1 required for evoked Ca2+ entry and control of flagellar function in sperm [J].
Carlson, AE ;
Westenbroek, RE ;
Quill, T ;
Ren, DJ ;
Clapham, DE ;
Hille, B ;
Garbers, DL ;
Babcock, DF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (25) :14864-14868
[4]
Immunocontraception of mammalian wildlife: ecological and immunogenetic issues [J].
Cooper, Desmond W. ;
Larsen, Elisabeth .
REPRODUCTION, 2006, 132 (06) :821-828
[5]
The potential use of sperm antigens as targets for immunocontraception past, present and future [J].
Frayne, J ;
Hall, L .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 1999, 43 (01) :1-33
[6]
Reversible, non-barrier male contraception:: Status and prospects [J].
Hoesl, CE ;
Saad, F ;
Pöppel, M ;
Altwein, JE .
EUROPEAN UROLOGY, 2005, 48 (05) :712-723
[7]
Whole-cell patch-clamp measurements of spermatozoa reveal an alkaline-activated Ca2+ channel [J].
Kirichok, Y ;
Navarro, B ;
Clapham, DE .
NATURE, 2006, 439 (7077) :737-740
[8]
KONG XB, 2008, INT J ANDROL 0220
[9]
Autoantibodies to ion channels at the neuromuscular junction [J].
Lang, B ;
Vincent, A .
AUTOIMMUNITY REVIEWS, 2003, 2 (02) :94-100
[10]
Larson JL, 1999, MOL REPROD DEV, V52, P445, DOI 10.1002/(SICI)1098-2795(199904)52:4<445::AID-MRD14>3.0.CO