Mehlmann Lisa M, Jaffe Laurinda A
Department of Cell Biology, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, Connecticut 06032, USA.
Reproduction. 2005 May;129(5):557-64. doi: 10.1530/rep.1.00638.
SRC family kinases (SFKs) function in initiating Ca2+ release at fertilization in several species in the vertebrate evolutionary line, but whether they play a similar role in mammalian fertilization has been uncertain. We investigated this question by first determining which SFK proteins are expressed in mouse eggs, and then measuring Ca2+ release at fertilization in the presence of dominant negative inhibitors. FYN and YES proteins were found in mouse eggs, but other SFKs were not detected; based on this, we injected mouse eggs with a mixture of FYN and YES Src homology 2 (SH2) domains. These SH2 domains were effective inhibitors of Ca2+ release at fertilization in starfish eggs, but did not inhibit Ca2+ release at fertilization in mouse eggs. Thus the mechanism by which sperm initiate Ca2+ release in mouse eggs does not depend on SH2 domain-mediated activation of an SFK. We also tested the small molecule SFK inhibitor SU6656, and found that it became compartmentalized in the egg cytoplasm, thus suggesting caution in the use of this inhibitor. Our findings indicate that although the initiation of Ca2+ release at fertilization of mammalian eggs occurs by a pathway that has many similarities to that in evolutionarily earlier animal groups, the requirement for SH2 domain-mediated activation of an SFK is not conserved.
在脊椎动物进化谱系的多个物种中,Src家族激酶(SFKs)在受精时启动钙离子释放过程中发挥作用,但它们在哺乳动物受精过程中是否发挥类似作用尚不确定。我们通过首先确定哪些SFK蛋白在小鼠卵母细胞中表达,然后在存在显性负性抑制剂的情况下测量受精时的钙离子释放,来研究这个问题。在小鼠卵母细胞中发现了FYN和YES蛋白,但未检测到其他SFKs;基于此,我们向小鼠卵母细胞注射了FYN和YES的Src同源2(SH2)结构域的混合物。这些SH2结构域是海星卵母细胞受精时钙离子释放的有效抑制剂,但并不抑制小鼠卵母细胞受精时的钙离子释放。因此,精子在小鼠卵母细胞中启动钙离子释放的机制并不依赖于SH2结构域介导的SFK激活。我们还测试了小分子SFK抑制剂SU6656,发现它在卵母细胞细胞质中发生区室化,因此在使用这种抑制剂时需谨慎。我们的研究结果表明,尽管哺乳动物卵母细胞受精时钙离子释放的启动途径与进化上更早的动物群体有许多相似之处,但对SH2结构域介导的SFK激活的需求并不保守。