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肿瘤坏死因子-α在体外诱导卵巢膜间质细胞聚集。

Tumor necrosis factor-alpha induces clustering in ovarian theca-interstitial cells in vitro.

作者信息

Zachow R J, Tash J S, Terranova P F

机构信息

Department of Physiology, University of Kansas Medical Center, Kansas City 66160-7401.

出版信息

Endocrinology. 1992 Dec;131(6):2503-13. doi: 10.1210/endo.131.6.1446592.

Abstract

Tumor necrosis factor-alpha (TNF) has been implicated in the regulation of steroidogenesis in theca-interstitial cells (TIC). The purpose of this study was to evaluate any change in TIC morphology during the time course of TNF-induced inhibition of LH-stimulated androstenedione production. Ovaries from immature hypophysectomized rats were enzymatically digested and highly purified TIC were obtained by density gradient centrifugation. TIC treated with TNF (0.1-10 ng/ml) demonstrated distinct clustering in the presence and absence of LH (50 ng/ml). The number of clusters and the mean area per cluster were greatest after 4 days as a result of treatment with 1 or 10 ng TNF/ml. In addition, a dose-dependent inhibition of LH-supported androstenedione production was induced by TNF. TNF also inhibited LH-induced androstenedione in TIC after 2, 4, or 6 days of continuous LH treatment, and TIC clustering still occurred. TIC clustering was impeded by the protein kinase inhibitor H7 at 10 microM; however, the protein kinase inhibitor, HA 1004 (5 microM), did not inhibit TNF-induced clustering in TIC. Since H7 blocked TNF induced clustering, but did not block TNF inhibition of LH stimulated androstenedione synthesis, it is suggested that alternate signal transduction pathways for TNF induced inhibition of LH-stimulated androstenedione and stimulation of clustering of TIC may exist. The results also indicate that the TNF-induced TIC clustering may be independent of the TNF-induced inhibition of LH-stimulated androstenedione production and states of LH-induced differentiation of TIC.

摘要

肿瘤坏死因子-α(TNF)与卵泡膜间质细胞(TIC)中类固醇生成的调节有关。本研究的目的是评估在TNF诱导LH刺激的雄烯二酮生成受抑制的时间过程中,TIC形态的任何变化。对未成熟垂体切除大鼠的卵巢进行酶消化,并通过密度梯度离心获得高度纯化的TIC。在有和没有LH(50 ng/ml)存在的情况下,用TNF(0.1 - 10 ng/ml)处理的TIC表现出明显的聚集。在用1或10 ng TNF/ml处理4天后,聚集簇的数量和每个簇的平均面积最大。此外,TNF诱导了LH支持的雄烯二酮生成的剂量依赖性抑制。在连续LH处理2、4或6天后,TNF也抑制了TIC中LH诱导的雄烯二酮生成,并且TIC聚集仍然发生。蛋白激酶抑制剂H7在10 microM时阻碍了TIC聚集;然而,蛋白激酶抑制剂HA 1004(5 microM)并未抑制TNF诱导的TIC聚集。由于H7阻断了TNF诱导的聚集,但未阻断TNF对LH刺激的雄烯二酮合成的抑制,提示可能存在TNF诱导的LH刺激的雄烯二酮抑制和TIC聚集刺激的替代信号转导途径。结果还表明,TNF诱导的TIC聚集可能独立于TNF诱导的LH刺激的雄烯二酮生成抑制以及LH诱导的TIC分化状态。

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