Role of protein tyrosine phosphorylation in the thapsigargin-induced intracellular Ca2+ store depletion during human sperm acrosome reaction

被引:25
作者
Dorval, W
Dufour, M
Leclerc, P
机构
[1] Univ Laval, Dept Obstet Gynecol, Quebec City, PQ G1L 3L5, Canada
[2] Univ Laval, Ctr Rech Biol Reprod, Quebec City, PQ G1L 3L5, Canada
[3] CHUQ, Ctr Rech, Quebec City, PQ G1L 3L5, Canada
[4] CHU Laval, Ctr Rech, Quebec City, PQ G1V 4G2, Canada
基金
加拿大健康研究院;
关键词
acrosome; calcium store; Ca2+-ATPase; capacitation; phosphotyrosine; HUMAN SPERMATOZOA; ZONA-PELLUCIDA; MOUSE SPERM; CALCIUM; CAPACITATION; PROGESTERONE; EXOCYTOSIS; RECEPTOR; INFLUX; CALRETICULIN;
D O I
10.1093/molehr/gag017
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
During human sperm capacitation, an increase in phosphotyrosine content of specific proteins results partially from an increase in the intracellular free Ca2+ concentrations. In the present study, the inter-regulation between protein phosphotyrosine content and the intracellular Ca2+ concentration during the thapsigargin treatment of capacitated human sperm was investigated. The involvement of a tyrosine kinase pathway in the thapsigargin-induced acrosome reaction was also investigated. In response to thapsigargin, two sperm subpopulations, called LR (low responsive) and HR (high responsive), according to their increase in intracellular Ca2+, were observed. In addition to their high increase in intracellular Ca2+, sperm from the HR population expressed a higher protein phosphotyrosine content, and a higher proportion (P < 0.05) of them underwent the acrosome reaction in response to thapsigargin, as compared with LR sperm. Although the tyrosine kinase inhibitor PP2 abolished the thapsigargin-induced increase in protein phosphotyrosine content, it did not affect the intracellular Ca2+ concentration or the percentage of acrosome-reacted sperm. The inability of an src-related tyrosine kinase inhibitor to block the thapsigargin-mediated Ca2+ increase and acrosomal exocytosis suggests that, during the acrosome reaction, the signalling pathway mediated by src-related tyrosine kinases is involved upstream of the capacitative Ca2+ entry.
引用
收藏
页码:125 / 131
页数:7
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