SIK2 and SIK3 Differentially Regulate Mouse Granulosa Cell Response to Exogenous Gonadotropins In Vivo.

IF 3.8 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM Endocrinology Pub Date : 2024-08-27 DOI:10.1210/endocr/bqae107
Emily T Hayes, Mariam Hassan, Oliwia Lakomy, Rachael Filzen, Marah Armouti, Marc Foretz, Noriyuki Tsumaki, Hiroshi Takemori, Carlos Stocco
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Abstract

Salt-inducible kinases (SIKs), a family of serine/threonine kinases, were found to be critical determinants of female fertility. SIK2 silencing results in increased ovulatory response to gonadotropins. In contrast, SIK3 knockout results in infertility, gonadotropin insensitivity, and ovaries devoid of antral and preovulatory follicles. This study hypothesizes that SIK2 and SIK3 differentially regulate follicle growth and fertility via contrasting actions in the granulosa cells (GCs), the somatic cells of the follicle. Therefore, SIK2 or SIK3 GC-specific knockdown (SIK2GCKD and SIK3GCKD, respectively) mice were generated by crossing SIK floxed mice with Cyp19a1pII-Cre mice. Fertility studies revealed that pup accumulation over 6 months and the average litter size of SIK2GCKD mice were similar to controls, although in SIK3GCKD mice were significantly lower compared to controls. Compared to controls, gonadotropin stimulation of prepubertal SIK2GCKD mice resulted in significantly higher serum estradiol levels, whereas SIK3GCKD mice produced significantly less estradiol. Cyp11a1, Cyp19a1, and StAR were significantly increased in the GCs of gonadotropin-stimulated SIK2GCKD mice. However, Cyp11a1 and StAR remained significantly lower than controls in SIK3GCKD mice. Interestingly, Cyp19a1 stimulation in SIK3GCKD was not statistically different compared to controls. Superovulation resulted in SIK2GCKD mice ovulating significantly more oocytes, whereas SIK3GCKD mice ovulated significantly fewer oocytes than controls. Remarkably, SIK3GCKD superovulated ovaries contained significantly more preantral follicles than controls. SIK3GCKD ovaries contained significantly more apoptotic cells and fewer proliferating cells than controls. These data point to the differential regulation of GC function and follicle development by SIK2 and SIK3 and supports the therapeutic potential of targeting these kinases for treating infertility or developing new contraceptives.

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SIK2和SIK3对小鼠体内颗粒细胞对外源性促性腺激素的反应有不同的调节作用。
盐诱导激酶(SIKs)是丝氨酸/苏氨酸激酶的一个家族,被发现是决定女性生育能力的关键因素。SIK2 沉默会导致对促性腺激素的排卵反应增强。与此相反,SIK3 基因敲除会导致不孕、促性腺激素不敏感以及卵巢无前卵泡和排卵前卵泡。本研究推测,SIK2 和 SIK3 通过对卵泡的体细胞--颗粒细胞(GCs)的不同作用,对卵泡的生长和生育能力进行不同的调节。因此,通过将 SIK 悬浮小鼠与 Cyp19a1pII-Cre 小鼠杂交,产生了 SIK2 或 SIK3 GC 特异性敲除(分别为 SIK2GCKD 和 SIK3GCKD)小鼠。生育力研究显示,SIK2GCKD小鼠6个月的幼仔累积量和平均窝产仔数与对照组相似,但SIK3GCKD小鼠的幼仔累积量和平均窝产仔数明显低于对照组。与对照组相比,对青春期前的 SIK2GCKD 小鼠进行促性腺激素刺激会导致血清雌二醇水平明显升高,而 SIK3GCKD 小鼠产生的雌二醇则明显降低。在促性腺激素刺激的 SIK2GCKD 小鼠的 GC 中,Cyp11a1、Cyp19a1 和 StAR 明显增加。然而,SIK3GCKD小鼠的Cyp11a1和StAR仍明显低于对照组。有趣的是,SIK3GCKD 小鼠的 Cyp19a1 刺激与对照组相比没有统计学差异。超排卵导致 SIK2GCKD 小鼠排出的卵母细胞明显多于对照组,而 SIK3GCKD 小鼠排出的卵母细胞明显少于对照组。值得注意的是,SIK3GCKD超排卵小鼠卵巢中的前房卵泡数量明显多于对照组。与对照组相比,SIK3GCKD 卵巢中凋亡细胞明显增多,增殖细胞明显减少。这些数据表明,SIK2 和 SIK3 对 GC 功能和卵泡发育有不同的调节作用,并支持以这些激酶为靶点治疗不孕症或开发新避孕药物的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Endocrinology
Endocrinology 医学-内分泌学与代谢
CiteScore
8.10
自引率
4.20%
发文量
195
审稿时长
2-3 weeks
期刊介绍: The mission of Endocrinology is to be the authoritative source of emerging hormone science and to disseminate that new knowledge to scientists, clinicians, and the public in a way that will enable "hormone science to health." Endocrinology welcomes the submission of original research investigating endocrine systems and diseases at all levels of biological organization, incorporating molecular mechanistic studies, such as hormone-receptor interactions, in all areas of endocrinology, as well as cross-disciplinary and integrative studies. The editors of Endocrinology encourage the submission of research in emerging areas not traditionally recognized as endocrinology or metabolism in addition to the following traditionally recognized fields: Adrenal; Bone Health and Osteoporosis; Cardiovascular Endocrinology; Diabetes; Endocrine-Disrupting Chemicals; Endocrine Neoplasia and Cancer; Growth; Neuroendocrinology; Nuclear Receptors and Their Ligands; Obesity; Reproductive Endocrinology; Signaling Pathways; and Thyroid.
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