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Mannosylated glycoconjugates on the surface of activated sperm in the giant freshwater prawn are crucial for sperm binding with the egg vitelline envelop

机译:在巨型淡水虾的活性精子表面上的甘露糖苷化的糖缀合物对于与卵vitelline包围的精子结合至关重要

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The unusual morphology and poorly defined acrosome-like structure in the mature sperm of the giant freshwater prawn Macrobrachium rosenbergii has led to difficulties in identifying the state of sperm activation. Mature distal vas deferens sperm (dVSp) can be activated by the calcium ionophore A23187 to show acrosome reaction-like enzymatic activities that increase their binding and penetration capabilities. However, these short-lived enzymatic activities limit their usefulness as a marker of sperm activation for further qualitative and quantitative analyses, leading to our examining the alterations in the exposure of sperm surface glycoconjugates both as markers of sperm activation and for their role in gamete interaction. Our results showed that after A23187 treatment, there was an increased exposure of mannosylated glycoconjugates on the sperm surface revealed by significant Concanavalin A (Con A) staining. Furthermore, sodium metaperiodate pre-treatment, Con A pre-incubation, or co-incubation with alpha-mannose monosaccharides all significantly reduced A23187-induced dVSp binding to the egg vitelline envelop, demonstrating the importance of sperm surface mannosylated glycoconjugates in the binding process. These same pre-treatments of sperm also resulted in the inhibition of the binding of soluble vitelline envelop proteins (MrVE) to both the sperm surface and to mannosylated dVSp protein bands. Therefore, the present study demonstrated the importance of the exposure of mannosylated glycoconjugates on the surface of activated dVSp, both as a reliable marker of sperm activation and as a binding factor in the gamete interaction process. Furthermore, these findings allow for a better understanding of the surface glycoconjugate-mediated interaction process between gametes in this species of prawn.
机译:罗氏沼虾成熟精子的异常形态和顶体样结构定义不清,导致难以确定精子激活状态。成熟的远端输精管精子(dVSp)可被钙离子载体A23187激活,表现出类似顶体反应的酶活性,从而增强其结合和穿透能力。然而,这些短命的酶活性限制了它们作为精子活化标记物用于进一步定性和定量分析的有效性,导致我们研究了精子表面糖缀合物暴露的变化,这既是精子活化标记物,也是它们在配子相互作用中的作用。我们的结果显示,A23187治疗后,显著的刀豆球蛋白A(Con A)染色显示精子表面甘露糖基化糖缀合物的暴露增加。此外,过高碘酸钠预处理、Con A预孵育或与α-甘露糖单糖共同孵育均显著降低A23187诱导的dVSp与卵黄膜的结合,证明精子表面甘露糖基化糖缀合物在结合过程中的重要性。对精子进行同样的预处理也会抑制可溶性卵黄膜蛋白(MrVE)与精子表面和甘露糖基化dVSp蛋白带的结合。因此,本研究证明了在活化的dVSp表面暴露甘露糖基化糖缀合物的重要性,它既是精子活化的可靠标志物,也是配子相互作用过程中的结合因子。此外,这些发现有助于更好地理解这种对虾配子间的表面糖缀合物介导的相互作用过程。

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