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孕酮对牛黄体细胞中bax和bcl-2表达及半胱天冬酶活性的影响。

Effect of progesterone on the expression of bax and bcl-2 and on caspase activity in bovine luteal cells.

作者信息

Liszewska E, Rekawiecki R, Kotwica J

机构信息

Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, P.O. Box 55, 10-718 Olsztyn, Poland.

出版信息

Prostaglandins Other Lipid Mediat. 2005 Dec;78(1-4):67-81. doi: 10.1016/j.prostaglandins.2005.03.003. Epub 2005 Jun 9.

Abstract

Bovine luteal cells from days 6-10 and 11-15 of the estrous cycle were exposed (6 h) to factors that support or disrupt steroidogenesis. The expression of bcl-2 and bax and level of active caspase-3 in cells was measured. Progesterone (P4) increased (P<0.01) while staurosporine decreased (P<0.01-P<0.001) bcl-2 expression at both stages of the estrous cycle studied. In cells from 11-15 days of the estrous cycle expression of bcl-2 was stimulated (P<0.05) by prostaglandin (PG)E2 and inhibited (P<0.01) by 3,3',4,4'-tertrachlorobiphenyl (PCB)-77. Treatment with aminoglutethimide (blocker of cytochrome P450scc; 1.5 x 10(-4)M), nitric oxide donor (spermine NONOate), and staurosporine increased bax expression in cells collected from both experimental periods. The influence of these factors was greater in cells from days 11-15 (P<0.001) than by cells on days 6-10 (P<0.05) of the estrous cycle. PCB-77 stimulated expression of bax in cells from 11-15 days of cycle (P<0.01) only. Treatment of luteal cells with P4 and PGE2 for 24 h decreased (P<0.05) level of active caspase-3 while aminoglutethimide (P<0.05), spermine NONOate (P<0.05), and staurosporine (P<0.001) increased caspase-3 activity in the cells. Moreover, P4 decreased (P<0.05) while staurosporine increased (P<0.01) the ratio of bax/bcl-2 at both stages of the cycle. Aminoglutethimide, spermine NONOate and PCB increased (0<0.05) this ratio in cells on days 11-15 of the cycle. These results suggest that P4 concentrations in luteal cells protects against apoptosis, while disruption of steroidogenesis and reduced ability of luteal cells to produce P4 can induce cell death.

摘要

将发情周期第6 - 10天和11 - 15天的牛黄体细胞暴露于(6小时)支持或破坏类固醇生成的因子中。检测细胞中bcl - 2和bax的表达以及活性caspase - 3的水平。在所研究的发情周期的两个阶段,孕酮(P4)均增加(P<0.01)bcl - 2表达,而星形孢菌素则降低(P<0.01 - P<0.001)bcl - 2表达。在发情周期11 - 15天的细胞中,前列腺素(PG)E2刺激(P<0.05)bcl - 2表达,而3,3',4,4'-四氯联苯(PCB)- 77抑制(P<0.01)bcl - 2表达。用氨鲁米特(细胞色素P450scc的阻滞剂;1.5×10(-4)M)、一氧化氮供体(精胺NONOate)和星形孢菌素处理均增加了两个实验时期收集的细胞中bax的表达。这些因子对发情周期11 - 15天细胞的影响大于对6 - 10天细胞的影响(P<0.001对P<0.05)。PCB - 77仅刺激发情周期11 - 15天细胞中bax的表达(P<0.01)。用P4和PGE2处理黄体细胞24小时降低了(P<0.05)活性caspase - 3的水平,而氨鲁米特(P<0.05)、精胺NONOate(P<0.05)和星形孢菌素(P<0.001)增加了细胞中caspase - 3的活性。此外,在发情周期的两个阶段,P4降低(P<0.05)而星形孢菌素增加(P<0.01)bax/bcl - 2的比值。氨鲁米特、精胺NONOate和PCB增加了(P<0.05)发情周期11 - 15天细胞中的这一比值。这些结果表明,黄体细胞中P4的浓度可保护细胞免受凋亡,而类固醇生成的破坏和黄体细胞产生P4能力的降低可诱导细胞死亡。

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