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c-Jun磷酸化抑制剂会阻碍绵羊原始卵泡的激活。

Inhibitors of c-Jun phosphorylation impede ovine primordial follicle activation.

作者信息

Bertoldo Michael J, Bernard Jérémy, Duffard Nicolas, Tsikis Guillaume, Alves Sabine, Calais Laure, Uzbekova Svetlana, Monniaux Danielle, Mermillod Pascal, Locatelli Yann

机构信息

INRA, UMR85 Physiologie de la Reproduction et des Comportements, Nouzilly 37380, France School of Women's and Children's Health, Discipline of Obstetrics and Gynaecology, University of New South Wales, Sydney, Australia

INRA, UMR85 Physiologie de la Reproduction et des Comportements, Nouzilly 37380, France MNHN, Laboratoire de la Réserve de la Haute Touche, Obterre 36290, France.

出版信息

Mol Hum Reprod. 2016 May;22(5):338-49. doi: 10.1093/molehr/gaw012. Epub 2016 Feb 7.

Abstract

STUDY HYPOTHESIS

Is the c-Jun-N-terminal kinase (JNK) pathway implicated in primordial follicle activation?

STUDY FINDING

Culture of ovine ovarian cortex in the presence of two different c-Jun phosphorylation inhibitors impeded pre-antral follicle activation.

WHAT IS KNOWN ALREADY

Despite its importance for fertility preservation therapies, the mechanisms of primordial follicle activation are poorly understood. Amongst different signalling pathways potentially involved, the JNK pathway has been previously shown to be essential for cell cycle progression and pre-antral follicle development in mice.

STUDY DESIGN, SAMPLES/MATERIALS, METHODS: Ovine ovarian cortex pieces were cultured with varying concentrations of SP600125, JNK inhibitor VIII or anti-Mullerian hormone (AMH) in the presence of FSH for 9 days. Follicular morphometry and immunohistochemistry for proliferating cell nuclear antigen (PCNA), apoptosis and follicle activation (Foxo3a) were assessed.

MAIN RESULTS AND THE ROLE OF CHANCE

Inhibition of primordial follicle activation occurred in the presence of SP600125, JNK inhibitor VIII and AMH when compared with controls (all P < 0.05) after 2 days of culture. However, only in the highest concentrations used was the inhibition of activation associated with induction of follicular apoptosis (P < 0.05). In growing follicles, PCNA antigen expression was reduced when the JNK inhibitors or AMH were used (P < 0.05 versus control), indicating reduced proliferation of the somatic compartment.

LIMITATIONS, REASONS FOR CAUTION: Although we evaluated the effects of inhibition of c-Jun phosphorylation on primordial follicle development, we did not determine the cellular targets and mechanism of action of the inhibitors.

WIDER IMPLICATIONS OF THE FINDINGS

These results are the first to implicate the JNK pathway in primordial follicle activation and could have significant consequences for the successful development of fertility preservation strategies and our understanding of primordial follicle activation.

LARGE SCALE DATA

n/a.

STUDY FUNDING AND COMPETING INTERESTS

Dr Michael J. Bertoldo and the laboratories involved in the present study were supported by a grant from 'Région Centre' (CRYOVAIRE, Grant number #320000268). There are no conflicts of interest to declare.

摘要

研究假设

c-Jun氨基末端激酶(JNK)通路与原始卵泡激活有关吗?

研究发现

在两种不同的c-Jun磷酸化抑制剂存在的情况下培养绵羊卵巢皮质,会阻碍窦前卵泡激活。

已知信息

尽管原始卵泡激活机制对生育力保存疗法很重要,但人们对此了解甚少。在可能涉及的不同信号通路中,JNK通路先前已被证明对小鼠的细胞周期进程和窦前卵泡发育至关重要。

研究设计、样本/材料、方法:将绵羊卵巢皮质块在促卵泡激素(FSH)存在的情况下,与不同浓度的SP600125、JNK抑制剂VIII或抗苗勒管激素(AMH)一起培养9天。评估卵泡形态测量以及增殖细胞核抗原(PCNA)、细胞凋亡和卵泡激活(Foxo3a)的免疫组织化学情况。

主要结果及偶然性的作用

与对照组相比,培养2天后,在存在SP600125、JNK抑制剂VIII和AMH的情况下,原始卵泡激活受到抑制(所有P<0.05)。然而,只有在使用的最高浓度下,激活抑制才与卵泡凋亡诱导相关(P<0.05)。在生长卵泡中,使用JNK抑制剂或AMH时,PCNA抗原表达降低(与对照组相比,P<0.05),表明体细胞区增殖减少。

局限性、注意事项:尽管我们评估了抑制c-Jun磷酸化对原始卵泡发育的影响,但我们没有确定抑制剂的细胞靶点和作用机制。

研究结果的更广泛意义

这些结果首次表明JNK通路与原始卵泡激活有关,可能对生育力保存策略的成功开发以及我们对原始卵泡激活的理解产生重大影响。

大规模数据

无。

研究资金与利益冲突

迈克尔·J·贝尔托尔多博士及参与本研究的实验室得到了“中央大区”(CRYOVAIRE,资助编号#320000268)的资助。无利益冲突声明。

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