Sugino N, Takiguchi S, Kashida S, Takayama H, Yamagata Y, Nakamura Y, Kato H
Department of Obstetrics and Gynecology, Yamaguchi University School of Medicine, Ube 755-8505, Japan.
Biol Reprod. 1999 Oct;61(4):1133-8. doi: 10.1095/biolreprod61.4.1133.
Superoxide radicals are known to inhibit progesterone production by luteal cells and have also been reported to cause apoptosis in various cells. The corpus luteum has an antioxidant enzyme to scavenge superoxide radicals: copper-zinc superoxide dismutase (Cu, Zn-SOD). However, it remains unknown how the decrease in intracellular Cu,Zn-SOD activity influences luteal function. This study was therefore undertaken to investigate whether suppression of intracellular Cu,Zn-SOD activity inhibits progesterone production by rat luteal cells and causes apoptosis. To suppress intracellular Cu, Zn-SOD activity, dispersed rat luteal cells were incubated with Cu, Zn-SOD antisense oligonucleotides. The 48-h treatment with antisense oligonucleotides (10 microM) inhibited Cu,Zn-SOD activity by 50% and Cu,Zn-SOD mRNA level by 30%, whereas sense oligonucleotides used as the control had no effect. Progesterone concentration in the medium was significantly decreased by the 48-h treatment with antisense oligonucleotides in the presence of hCG, and this inhibitory effect was completely blocked by the simultaneous addition of N-acetyl-L-cysteine, an antioxidant. Treatment with antisense oligonucleotides caused no significant change in the percentage of apoptotic cells as morphologically evaluated by the nuclear staining with Hoechst dye. In conclusion, the decrease in intracellular Cu, Zn-SOD activities inhibits progesterone production by rat luteal cells, which may be mediated by superoxide radicals, suggesting that intracellular Cu,Zn-SOD plays important roles in the regulation of luteal function.
已知超氧自由基可抑制黄体细胞产生孕酮,并且也有报道称其可导致多种细胞发生凋亡。黄体具有一种抗氧化酶来清除超氧自由基:铜锌超氧化物歧化酶(Cu, Zn-SOD)。然而,细胞内Cu,Zn-SOD活性的降低如何影响黄体功能仍不清楚。因此,本研究旨在探讨抑制细胞内Cu,Zn-SOD活性是否会抑制大鼠黄体细胞产生孕酮并导致凋亡。为了抑制细胞内Cu,Zn-SOD活性,将分散的大鼠黄体细胞与Cu,Zn-SOD反义寡核苷酸一起孵育。用反义寡核苷酸(10 microM)处理48小时可使Cu,Zn-SOD活性降低50%,Cu,Zn-SOD mRNA水平降低30%,而用作对照的正义寡核苷酸则没有效果。在hCG存在的情况下,用反义寡核苷酸处理48小时可使培养基中的孕酮浓度显著降低,并且这种抑制作用可被同时添加的抗氧化剂N-乙酰-L-半胱氨酸完全阻断。用反义寡核苷酸处理后,通过Hoechst染料进行核染色在形态学上评估的凋亡细胞百分比没有显著变化。总之,细胞内Cu,Zn-SOD活性的降低会抑制大鼠黄体细胞产生孕酮,这可能是由超氧自由基介导的,表明细胞内Cu,Zn-SOD在黄体功能调节中起重要作用。