Bravo Anita, Quilaqueo Nelson, Jofré Ignacio, Villegas Juana V
Center of Reproductive Biotechnology - Scientific and Technological Bioresource Nucleus (CEBIOR - BIOREN), Universidad de La Frontera, Temuco, Chile.
Department of Internal Medicine, Faculty of Medicine, Universidad de La Frontera, Temuco, Chile.
Andrologia. 2021 Mar;53(2):e13907. doi: 10.1111/and.13907. Epub 2020 Dec 1.
In many cell types, the potential of reactive oxygen species to induce death processes has been largely demonstrated. Studies in spermatozoa have associated the imbalance of reactive oxygen species and phosphatidylserine externalisation as an apoptosis marker. However, the lack of consensus about time effect in the joint expression of these and other death markers has made it difficult to understand the set of mechanisms influenced beyond the concentration effect of reactive oxygen species to stimulate cell death. Here, the plasma membrane permeability and integrity, phosphatidylserine externalisation and mitochondrial membrane potential were jointly evaluated as death markers in human spermatozoa stimulated with H O . The results showed a profound and sustained effect of dissipation in the mitochondrial membrane potential and an increased phosphatidylserine externalisation in human spermatozoa exposed to 3 mmol of H O at 30 min. This was followed by an increased membrane permeability after 45 min. The last observed event was the loss of cell membrane integrity at 60 min. In conclusion, mitochondria are rapidly affected in human spermatozoa exposed to reactive oxygen species, with the barely detectable mitochondrial membrane potential coexisting with the high phosphatidylserine externalisation in cells with normal membrane permeability.
在许多细胞类型中,活性氧诱导细胞死亡过程的潜力已得到充分证明。对精子的研究已将活性氧失衡与磷脂酰丝氨酸外化作为细胞凋亡标志物联系起来。然而,对于这些及其他死亡标志物联合表达中的时间效应缺乏共识,这使得难以理解除活性氧浓度效应之外影响刺激细胞死亡的一系列机制。在此,将质膜通透性和完整性、磷脂酰丝氨酸外化及线粒体膜电位作为用H₂O₂刺激的人类精子中的死亡标志物进行联合评估。结果显示,在30分钟时,暴露于3 mmol H₂O₂的人类精子中线粒体膜电位的耗散具有深刻且持续的影响,磷脂酰丝氨酸外化增加。45分钟后膜通透性增加。最后观察到的事件是60分钟时细胞膜完整性丧失。总之,暴露于活性氧的人类精子中线粒体迅速受到影响,在膜通透性正常的细胞中,几乎检测不到的线粒体膜电位与高磷脂酰丝氨酸外化并存。