首页> 外文期刊>Journal of reproduction and fertility >Control of extracellular matrix remodelling within ovarian tissues: localization and regulation of gene expression of plasminogen activator inhibitor type-1 within the ovine corpus luteum
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Control of extracellular matrix remodelling within ovarian tissues: localization and regulation of gene expression of plasminogen activator inhibitor type-1 within the ovine corpus luteum

机译:卵巢组织内细胞外基质重塑的控制:黄体中纤溶酶原激活物抑制剂1型的基因表达的定位和调控

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Extensive extracellular matrix remodelling occurs within the lifespan of the corpus luteum, particularly during corpus luteum formation and regression. A major mechanism for the regulation of extracellular matrix remodelling is via local production of specific proteinase inhibitors, such as the serine proteinase inhibitor plasminogen activator inhibitor type-1 (PAI-1). The objective of the present study was to characterize the localization, ontogeny and regulation of PAI-1 expression within ovine corpora lutea. Urokinase binding activity was detected within medium conditioned by ovine luteal cells. Production of PAI-1 by ovine luteal cells was confirmed by immunoprecipitating it from labelled proteins in culture medium. mRNA encoding PAI-1 was present within developing (day 3), mature (day 10) and regressing (30 h after prostaglandin F2伪 injection on day 10 after the onset of oestrus) corpora lutea as demonstrated by in situ hybridization. The ontogeny of PAI-1 mRNA expression was characterized within corpora lutea collected on days 3, 7, 10, 13 and 16 after the onset of oestrus (n = 4, 4, 4, 3 and 4, respectively). Expression of PAI-1 mRNA did not differ during the luteal phase (P= 0.06), although a trend for an increase in the amount of PAI-1 mRNA was observed on day 16. Expression of PAI-1 mRNA was also examined during luteal regression in corpora lutea collected 0, 6, 12, 24 and 36 h after injection of prostaglandin F2伪 on day 10 after the onset of oestrus (n = 4 at each time). Relative PAI-1 mRNA concentrations changed significantly during luteolysis induced by prostaglandin F2伪 (P = 0.0002). Administration of prostaglandin F2伪 resulted in a transient sevenfold increase in PAI-1 mRNA 6 h after injection (P = 0.0001) but by 12 h the amounts had returned to values similar to those detected on day 10. We conclude that PAI-1 is a major secretory product of ovine luteal cells and that a transient increase in PAI-1 mRNA occurs during luteolysis induced by prostaglandin F2伪. PAI-1 probably plays a key local role in the control of extracellular proteolysis during the luteal phase.
机译:广泛的细胞外基质重塑发生在黄体的寿命内,特别是在黄体形成和消退期间。调节细胞外基质重塑的主要机制是通过局部产生特定的蛋白酶抑制剂,例如丝氨酸蛋白酶抑制剂纤溶酶原激活物抑制剂1型(PAI-1)。本研究的目的是表征羊黄体中PAI-1表达的定位,个体发育和调控。在绵羊黄体细胞调节的培养基中检测到尿激酶结合活性。通过从培养基中的标记蛋白免疫沉淀来确认羊黄体细胞产生PAI-1。通过原位杂交证实,编码PAI-1的mRNA存在于发育期(第3天),成熟(第10天)和消退(发情后第10天注射前列腺素F2α后30小时)体内。在发情发生后第3、7、10、13和16天收集的黄体内表征PAI-1 mRNA表达的个体发育(分别为n = 4、4、4、3和4)。尽管在第16天观察到PAI-1 mRNA的表达有增加的趋势,但在黄体期PAI-1 mRNA的表达没有差异(P = 0.06)。发情后第10天注射前列腺素F2α后0、6、12、24和36小时收集黄体消退(每次n = 4)。在前列腺素F2α引起的黄体溶解过程中,相对PAI-1 mRNA的浓度发生了显着变化(P = 0.0002)。注射前列腺素F2α导致注射后6 h PAI-1 mRNA瞬时增加7倍(P = 0.0001),但到12 h时PAI-1 mRNA的值恢复到与第10天检测到的值相似。我们得出结论,PAI-1为是绵羊黄体细胞的主要分泌产物,在前列腺素F2α引起的黄体溶解过程中,PAI-1 mRNA出现瞬时增加。在黄体期,PAI-1可能在控制细胞外蛋白水解中起着关键的局部作用。

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