Involvement of an F-actin skeleton on the acrosome reaction in guinea pig spermatozoa

被引:0
|
作者
Hernández-González, EO [1 ]
Lecona-Valera, AN [1 ]
Escobar-Herrera, J [1 ]
Mújica, A [1 ]
机构
[1] Inst Politecn Nacl, CINVESTAV, Ctr INvest Estudios Avanzados, Dept Biol Celular, Mexico City 07000, DF, Mexico
来源
CELL MOTILITY AND THE CYTOSKELETON | 2000年 / 46卷 / 01期
关键词
plasma and outer acrosomal membrane skeletons; spectrin; streptolysin O-permeabilized spermatozoa; cytochalasin D; phalloidin; exocytosis;
D O I
10.1002/(SICI)1097-0169(200005)46:1<43::AID-CM5>3.0.CO;2-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The acrosome reaction (AR) is a regulated exocytotic process. In several cell types, an actin network situated under the plasma membrane (PM) acts as a physical barrier to prevent this exocytosis. In seeking a function for a cortical skeleton in guinea pig spermatozoa, the PM and the outer acrosomal membrane (OAM) were investigated for the presence of F-actin and spectrin, proteins generally found in cell cortical skeletons. Both membrane types were visualized in whole-mount preparations by electron microscopy. PM proteins gave positive reaction to the Na+,K+-ATPase antibody and the OAM proteins did not react to the antibody. Furthermore, a Triton X-100-resistant skeleton was obtained from both membrane types. Using gold immunoelectron microscopy, F-actin was visualized in the PM and in the OAM skeletons, while spectrin was only detected in the PM skeleton. The presence of an F-actin cortical skeleton in the sperm PM suggests that F-actin may be involved in the AR. The significantly higher number of AR elicited by cytochalasin D (Cyt-D) treatment(P < 0.005) and data showing a significant (P > 0.03) decrease in F-actin relative concentration in capacitating spermatozoa, agree with this suggestion. Furthermore, the proposal is strengthened by the fact that stabilization of F-actin by phalloidin (Ph) significantly (P > 0.01) diminished AR induced by Ca2+ in a streptolysin O (SLO)-permeabilized sperm model. (C) 2000 Wiley-Liss, Inc.
引用
收藏
页码:43 / 58
页数:16
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