首页> 外文期刊>Tissue and Cell >Possible involvement of transforming growth factor-beta 1 and transforming growth factor-beta receptor type II during luteinization in the marmoset ovary.
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Possible involvement of transforming growth factor-beta 1 and transforming growth factor-beta receptor type II during luteinization in the marmoset ovary.

机译:在the猴卵巢中黄体化过程中可能涉及转化生长因子-β1和转化生长因子-β受体II型。

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The expression of transforming growth factor-beta 1 (TGF-beta 1), and transforming growth factor-beta receptor type II (T beta R-II), were evaluated in periovulatory marmoset ovaries. Histochemical methods were used, in particular double-labelling techniques, in order to correlate growth factor/receptor expression with proliferation (Ki 67), apoptosis (TUNEL method) and luteinization (3 beta-hydroxysteroid dehydrogenase (3 beta-HSD)). The latter was used as a luteinization marker. Periovulatory ovaries are especially suited for studying all aspects since they typically consist of small non-luteinized follicles, large luteinizing follicles and corpora lutea accessoria (Clas), which have developed from large luteinizing follicles. TGF-beta 1 and T beta R-II expression was found in luteinizing theca cells of large periovulatory follicles and in all luteal cells of Clas. Non-luteinized theca cells, including those of small follicles were always devoid of any immunostaining. Granulosa cells of small follicles were immunopositive for T beta R-II. Large follicles with granulosa cell immunoreactivity of both antibodies coexisted with non-reactive follicles of comparable size. The highest activity of the luteal marker enzyme 3 beta-HSD was co-localized in the same cells that expressed TGF-beta 1 and T beta R-II. The double-labelling experiments revealed that TGF-beta 1 and T beta R-II expression is not correlated with proliferation or apoptosis of follicular cells. Our results indicate that TGF-beta 1 and T beta R-II participate in differentiation processes, i.e. luteinization, rather than proliferation. In particular, the dynamics of T beta R-II expression appear highly related to the process of luteinization.
机译:在排卵期mar猴卵巢中评估了转化生长因子-beta 1(TGF-beta 1)和转化生长因子-beta受体II型(T beta R-II)的表达。为了使生长因子/受体表达与增殖(Ki 67),细胞凋亡(TUNEL方法)和黄体化(3β-羟类固醇脱氢酶(3β-HSD))相关,使用了组织化学方法,特别是双标记技术。后者用作黄体化标记。围排卵期的卵巢特别适合研究各个方面,因为它们通常由小的未黄素化的卵泡,较大的黄素化的卵泡和黄体附件(Clas)组成,后者从大型的黄素化的卵泡发育而来。 TGF-beta 1和T beta R-II表达在黄体化大卵泡期卵泡的theca细胞和Clas的所有黄体细胞中都有。未黄化的theca细胞,包括小卵泡细胞,始终没有任何免疫染色。小卵泡颗粒细胞对TβR-II呈免疫阳性。具有两种抗体的颗粒细胞免疫反应性的大卵泡与相当大小的非反应性卵泡共存。黄体标记酶3 beta-HSD的最高活性共定位在表达TGF-beta 1和T beta R-II的相同细胞中。双重标记实验表明,TGF-beta 1和T beta R-II表达与滤泡细胞的增殖或凋亡无关。我们的结果表明,TGF-β1和TβR-II参与分化过程,即黄体化而不是增殖。特别是,T beta R-II表达的动力学似乎与黄体化过程高度相关。

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