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氧化应激和半胱天冬酶-8、-9 和 -3 的活性参与了卵丘颗粒细胞冷冻保存诱导的细胞凋亡。

Oxidative stress and activities of caspase-8, -9, and -3 are involved in cryopreservation-induced apoptosis in granulosa cells.

机构信息

Department of Reproductive Medicine, Jinan Central Hospital Affiliated to Shandong University, 105 Jiefang Road, Jinan 250000, China.

出版信息

Eur J Obstet Gynecol Reprod Biol. 2013 Jan;166(1):52-5. doi: 10.1016/j.ejogrb.2012.09.011. Epub 2012 Sep 21.

Abstract

OBJECTIVE

The aim of this study is to determine whether the oxidative stress and the activities of caspase-8, -9, and -3 are involved in cryopreservation-induced apoptosis in granulosa cells.

STUDY DESIGN

Granulosa cells from rats were cryopreserved with or without genistein. The level of superoxide dismutase (SOD) was measured. Moreover, the expressions of caspase-8, -9, and -3 in both mRNA and protein were measured.

RESULTS

The SOD level in cryopreserved granulosa cells was significantly lower than that in a fresh control group, and the levels of caspase-8, -9, and -3 expression in both mRNA and protein in cryopreserved granulosa cells were significantly higher than those of fresh control granulosa cells. Furthermore, the levels of caspase-8 and -3 expression in both mRNA and protein of granulosa cells cryopreserved in presence of genistein were significant lower than those of granulosa cells cryopreserved in absence of genistein.

CONCLUSION

Oxidative stress induced by cryopreservation in granulosa cells is involved in the activation of caspase-8 and -3. Cryopreservation-induced apoptosis in granulosa cells is mediated, at least in part, by activation of caspase-8, -9, and -3 dependent apoptotic pathways.

摘要

目的

本研究旨在探讨氧化应激及胱天蛋白酶-8、-9、-3 的活性是否参与了卵丘颗粒细胞的冻存凋亡。

设计

采用有无染料木黄酮存在的情况下对大鼠卵丘颗粒细胞进行冻存。测定超氧化物歧化酶(SOD)的水平。此外,还测定了胱天蛋白酶-8、-9、-3 在 mRNA 和蛋白水平的表达。

结果

冻存的卵丘颗粒细胞中的 SOD 水平明显低于新鲜对照组,且冻存的卵丘颗粒细胞中胱天蛋白酶-8、-9、-3 在 mRNA 和蛋白水平的表达均明显高于新鲜对照组的卵丘颗粒细胞。此外,在有染料木黄酮存在的情况下冻存的卵丘颗粒细胞中胱天蛋白酶-8 和 -3 在 mRNA 和蛋白水平的表达明显低于无染料木黄酮存在的情况下冻存的卵丘颗粒细胞。

结论

卵丘颗粒细胞冻存诱导的氧化应激参与了胱天蛋白酶-8 和 -3 的激活。卵丘颗粒细胞的冻存诱导凋亡至少部分是通过激活胱天蛋白酶-8、-9、-3 依赖的凋亡途径介导的。

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