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首页> 外文期刊>Animal Reproduction Science >Transcription factor NF- kappa B (p50/p50, p65/p65) controls porcine ovarian cells functions.
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Transcription factor NF- kappa B (p50/p50, p65/p65) controls porcine ovarian cells functions.

机译:转录因子NF-κB(p50 / p50,p65 / p65)控制猪卵巢细胞功能。

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摘要

The aim of these in vitro studies was to examine the involvement of transcription factor NF- kappa B (p50/p50, p65/p65) and FSH in control of porcine ovarian granulosa cells functions and the possible role of dimers p50/p50, p65/p65 in mediating FSH actions on these cells. Monolayer of primary granulosa cells was transfected with plasmids encoding human p50 cDNA and p65 cDNA, and cultured with or without addition of FSH (0, 1, 10 or 100 ng/ml). The accumulation of proteins p50 and p65, as well as of proliferation markers (PCNA and MAPK/ERK1,2) and marker of apoptosis (Bax) in cells was detected by using SDS-PAGE-Western immunoblotting and immunocytochemistry. DNA fragmentation was evaluated by TUNEL assay. Release of hormones insulin-like growth factor I (IGF-I), progesterone (P4), oxytocin (OT), prostaglandins E2 (PGE2) and F2 alpha (PGF2 alpha ) was measured by using RIA. We observed, that p50/p50 promoted the accumulation of PCNA, MAPK/ERK1,2, the release of OT, PGF2 alpha ; inhibited the occurrence of TdT-positive cells, the release of IGF-I and P4, and did not influence the accumulation of Bax and the release of PGE2. p65/p65 enhanced the accumulation of PCNA, MAPK/ERK1,2 and Bax, the release of IGF-I, OT, PGE2 and PGF2 alpha ; decreased the percentage of cell containing TdT and did not affect the release of P4. FSH stimulated the accumulation of PCNA, MAPK/ERK1,2 and Bax, the release of IGF-I, OT, P4, PGE2; but reduced the proportion of TdT-positive cells and the release of PGF2 alpha . These observations suggest (1) the involvement of NF- kappa B (p50/p50) in stimulation of proliferation, inhibition of apoptosis and in either stimulation (OT, PGE2) or inhibition (IGF-I, P4, but not PGF2) of hormones release by porcine ovarian granulosa cells; (2) the involvement of NF- kappa B (p65/p65) in stimulation of proliferation and mitochondrial/Bax-related apoptosis, inhibition of nuclear/TdT-related apoptosis and in stimulation of ovarian hormones (IGF-I, OT, PGE2, PGF2 alpha , but not P4) release; (3) the role of FSH in up-regulation of both ovarian cell proliferation and mitochondrial/Bax-related apoptosis, in inhibition of nuclear/TdT-related apoptosis, in promotion of IGF-I, P4, OT, PGE2 and suppression of PGF2 alpha release by porcine ovarian cells. The majority of results demonstrates the involvement of NF- kappa B (p50/p50 and p65/p65) and FSH in control of basic ovarian functions (proliferation, apoptosis, and secretory activity), but not the functional interrelationships between these regulators.
机译:这些体外研究的目的是研究转录因子NF-κB(p50 / p50,p65 / p65)和FSH在控制猪卵巢颗粒细胞功能中的作用以及其可能的作用。二聚体p50 / p50,p65 / p65介导这些细胞的FSH作用。用编码人p50 cDNA和p65 cDNA的质粒转染单层原代颗粒细胞,并在有或没有添加FSH(0、1、10或100 ng / ml)的条件下进行培养。使用SDS-PAGE-Western免疫印迹法和免疫细胞化学法检测细胞中p50和p65蛋白的积累,以及增殖标志物(PCNA和MAPK / ERK1,2)和凋亡标志物(Bax)的积累。通过TUNEL测定法评估DNA片段化。释放胰岛素样生长因子I(IGF-1),孕酮(P 4 ),催产素(OT),前列腺素E 2 (PGE 2 < / sub>)和F 2 alpha (PGF 2 alpha )通过RIA测量。我们观察到,p50 / p50促进了PCNA,MAPK / ERK1,2的积累,OT,PGF 2 alpha 的释放;抑制TdT阳性细胞的发生,IGF-I和P 4 的释放,并且不影响Bax的积累和PGE 2 的释放。 p65 / p65增强了PCNA,MAPK / ERK1,2和Bax的积累,促进了IGF-1,OT,PGE 2 和PGF 2 alpha 的释放;降低了含有TdT的细胞百分比,并且不影响P 4 的释放。 FSH刺激PCNA,MAPK / ERK1,2和Bax的积累,IGF-I,OT,P 4 ,PGE 2 的释放;但降低了TdT阳性细胞的比例和PGF 2 alpha 的释放。这些观察结果表明:(1)NF-κB(p50 / p50)参与了增殖刺激,凋亡抑制以及刺激(OT,PGE 2 )或抑制(IGF-1,猪卵巢颗粒细胞释放激素的P 4 而不是PGF 2 ); (2)NF-κB(p65 / p65)参与刺激增殖和线粒体/ Bax相关凋亡,抑制核/ TdT相关凋亡以及刺激卵巢激素(IGF-1,OT,PGE < sub> 2 ,PGF 2 alpha ,但不发布P 4 ); (3)FSH在上调卵巢细胞增殖和线粒体/ Bax相关凋亡中的作用,在抑制核/ TdT相关凋亡中的作用,促进IGF-I,P 4 ,OT,PGE 2 和猪卵巢细胞抑制PGF 2 alpha 释放。大多数结果表明,NF-κB(p50 / p50和p65 / p65)和FSH参与了基本卵巢功能(增殖,凋亡和分泌活性)的控制,但没有涉及这些调节因子之间的功能相互关系。

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