双氢睾酮对大鼠原代卵泡颗粒细胞抗苗勒管激素表达的影响

王美玲 董玉婷 叶晓锋 黑常春 蔡玉芳 孔斌 赵承军 常青

解剖学报 ›› 2020, Vol. 51 ›› Issue (3) : 367-372.

PDF(5712 KB)
欢迎访问《解剖学报》官方网站!今天是 English
PDF(5712 KB)
解剖学报 ›› 2020, Vol. 51 ›› Issue (3) : 367-372. DOI: 10.16098/j.issn.0529-1356.2020.03.009
细胞和分子生物学

双氢睾酮对大鼠原代卵泡颗粒细胞抗苗勒管激素表达的影响

  • 王美玲1 董玉婷1 叶晓锋2 黑常春1 蔡玉芳1 孔斌1 赵承军1 常青1* 
作者信息 +

Effects of dihydrotestosterone on the expression of anti-Müllerian hormone in primary follicular granulosa cells in rats

  • WANG Mei-ling1 DONG Yu-ting1 YE Xiao-feng2 HEI Chang-chun1 CAI Yu-fang1 KONG Bin1 ZHAO Cheng-jun1 CHANG Qing1*
Author information +
文章历史 +

摘要

目的  探讨双氢睾酮(DHT)对大鼠原代卵泡颗粒细胞抗苗勒管激素(AMH)表达的影响。  方法  从95只21 d SD雌性大鼠中提取颗粒细胞原代培养48 h后,先用HE染色检测细胞形态,卵泡刺激素受体(FSHR)细胞免疫荧光检测细胞纯度;然后根据干预方法和实验的不同,随机将细胞分为对照组(无药物干预)、10-8mol/L DHT组、10-5mol/L DHT组,2×10-5mol/ L蛋白激酶B(Akt)抑制剂(MK-2206 2Hcl)组和10-8mol/L DHT+2×10-5mol/L MK-2206 2Hcl组,分别使用相应浓度的试剂干预细胞3 h。干预完成后,细胞免疫荧光染色观察AMH表达的部位和变化;Western blotting测定不同组的AMH、Akt、p-Akt蛋白表达量。  结果 大鼠原代卵泡颗粒细胞的纯度为93.33%±3.09%,AMH表达在大鼠原代卵泡颗粒细胞膜和细胞质中;与对照组相比,10-8 mol/L DHT和10-5 mol/L DHT均可使颗粒细胞AMH表达增加(P<0.05),但这两个浓度的DHT对颗粒细胞AMH的表达影响差异无显著性(P>0.05);与对照组相比,10-8 mol/L DHT可以使p-Akt、AMH表达升高,2×10-5 MK-2206 2Hcl使AMH表达降低(P<0.05);与2×10-5MK-2206 2Hcl相比,10-8mol/L DHT+2×10-5 MK-2206 2Hcl处理组AMH表达升高(P<0.05)。  结论  DHT可以上调大鼠原代卵泡颗粒细胞AMH的表达,这种作用可能与Akt信号通路有关。

Abstract

Objective To explore how dihydrotestosterone (DHT) affects the expression of anti-Müllerian hormone (AMH) in primary rat follicular granulosa cells, and then provides a new experimental basis for the role of DHT and AMH in follicular development.  Methods  Granulosa cells was extracted from the ovaries of 95 21 days SD female rats for primary culture. Firstly, cell morphology were detected by HE staining and follicke stimulating hormone receptor(FSHR) immunofluorescence detected cell purity after 48 hours of cell culture. Then, cells were randomly divided into control group (without drug intervention), 10-8mol/L DHT group, 10-5mol/L DHT group, 2×10-5 protein kinase B(Akt) inhibitor (MK-2206 2Hcl) group and 10-8mol/L DHT+ 2×10-5 mol/L MK-2206 2Hcl group according to different intervention method  and experiments,corresponding concentrations were used in each group to intervene cells for 3 hours. After intervention, sites and expression changes of AMH were detected by immunofluorescence. Changes of AMH, Akt and p-Akt were detected by Western blotting.   Results  Immunofluorescence showed that the purity of primary follicular granule cells in rats was 93.33%±3.09%,and AMH was expressed in the membrane and cytoplasm of primary follicular granule cells in rats; Compared with the control group, both 10-8 mol/L DHT and 10-5 mol/L DHT increased the expression of AMH in granulosa cells (P<0.05),but there was no difference in the effect of these two concentrations of DHT on the expression of AMH in granulosa cells (P>0.05); Compared with the control group, 10-8 mol/L DHT increased p-Akt and AMH expression, and 2×10-5MK-2206 2Hcl decreased AMH expression (P<0.05); Compared with the 2×10-5 MK-2206 2Hcl, AMH expression was increased in the 10-8 mol/L DHT+2×10-5 MK-2206 2Hcl treatment group (P<0.05).   Conclusion  DHT can up-regulate the expression of AMH in primary follicular granulosa cells in rats, and this effect may be related to the Akt signaling pathway.

关键词

双氢睾酮 / 抗苗勒管激素 / 卵泡颗粒细胞 / 免疫荧光 / 免疫印迹法 / 大鼠

Key words

Dihydrotestosterone / Anti-Müllerian hormone / Follicular granulosa cell / Immunofluorescence / Western blotting / Rat

引用本文

导出引用
王美玲 董玉婷 叶晓锋 黑常春 蔡玉芳 孔斌 赵承军 常青. 双氢睾酮对大鼠原代卵泡颗粒细胞抗苗勒管激素表达的影响[J]. 解剖学报. 2020, 51(3): 367-372 https://doi.org/10.16098/j.issn.0529-1356.2020.03.009
WANG Mei-ling DONG Yu-ting YE Xiao-feng HEI Chang-chun CAI Yu-fang KONG Bin ZHAO Cheng-jun CHANG Qing. Effects of dihydrotestosterone on the expression of anti-Müllerian hormone in primary follicular granulosa cells in rats[J]. Acta Anatomica Sinica. 2020, 51(3): 367-372 https://doi.org/10.16098/j.issn.0529-1356.2020.03.009
中图分类号: R329   

参考文献

[1] Yuan LJ,Ren JX,Ji HY,et al. Expression of transforming growth factor-β and Smad4 in ovarian granulosa cells in menopausal transitional rat [J]. Acta Anatomica Sinica,2018, 49(1): 108-112.(in Chinese)
袁丽娟, 任君旭, 姬宏宇, 等. 转化生长因子-β和Smad4在绝经过渡期大鼠卵巢颗粒细胞中的表达[J]. 解剖学报, 2018, 49(1): 108-112.
[2] Gleicher N, Barad DH. Dehydroepiandrosterone (DHEA) supplementation in diminished ovarian reserve (DOR)[J]. Reprod Biol Endocrinol, 2011, 9: 67.
[3] Panjari M,Davis SR. DHEA therapy for women:effect on sexual function and wellbeing [J]. Hum Reprod Update,2007(3): 239-248.
[4] Narkwichean A, Jayaprakasan K, Maalouf WE, et al. Effects of dehydroepiandrosterone on in vivo ovine follicular development[J]. Hum Reprod, 2014, 29(1): 146-154.
[5] Abbott DH, Vepraskas SH, Horton TH, et al. Accelerated episodic luteinizing hormone release accompanies blunted progesterone regulation in PCOS-like female rhesus monkeys (Macaca Mulatta) exposed to testosterone during early-to-mid gestation[J]. Neuroendocrinology, 2018, 107(2): 133-146.
[6] Roy S, Gandra D, Seger C, et al. Oocyte-derived factors (GDF9 and BMP15) and FSH regulate AMH expression via modulation of H3K27AC in granulosa cells[J]. Endocrinology, 2018, 159(9): 3433-3445.
[7] Witchel SF, Burghard AC, Tao RH, et al. The diagnosis and treatment of PCOS in adolescents: an update[J]. Curr Opin Pediatr, 2019, 31(4): 562-569.
[8] Zhang Y, Wang SF, Zheng JD, et al. Effects of testosterone on the expression levels of AMH, VEGF and HIF-1alpha in mouse granulosa cells[J]. Exp Ther Med, 2016, 12(2): 883-888.
[9] Laird M, Thomson K, Fenwick M, et al. Androgen stimulates growth of mouse preantral follicles in vitro: interaction with follicle-stimulating hormone and with growth factors of the TGFbeta superfamily[J]. Endocrinology, 2017, 158(4): 920-935.
[10] Pierre A, Estienne A, Racine C, et al. The bone morphogenetic protein 15 up-regulates the antimullerian hormone receptor expression in granulosa cells[J]. J Clin Endocrinol Metab, 2016, 101(6): 2602-2611. 
[11] Lovekamp TN, Davis BJ. Mono-(2-ethylhexyl) phthalate suppresses aromatase transcript levels and estradiol production in cultured rat granulosa cells[J]. Toxicol Appl Pharmacol, 2001, 172(3): 217-224.

[12] Pinola P, Morin-Papunen LC, Bloigu A, et al. Anti-Müllerian hormone: correlation with testosterone and oligo- or amenorrhoea in female adolescence in a population-based cohort study[J]. Hum Reprod, 2014, 29(10): 2317-2325.

[13] Filatov M, Khramova Y, Parshina E, et al. Influence of gonadotropins on ovarian follicle growth and development in vivo and in vitro[J]. Zygote, 2017, 25(3): 235-243.
[14] Yang MY, Cushman RA, Fortune JE. Anti-Müllerian hormone inhibits activation and growth of bovine ovarian follicles in vitro and is localized to growing follicles[J]. Mol Hum Reprod, 2017, 23(5): 282-291.

[15] Xiang C, Li J, Hu L, et al. Hippo signaling pathway reveals a spatio-temporal correlation with the size of primordial follicle pool in mice[J]. Cell Physiol Biochem, 2015, 35(3): 957-968.

 [16] Sonigo C, Beau Ⅰ, Grynberg M, et al. AMH prevents primordial ovarian follicle loss and fertility alteration in cyclophosphamide-treated mice[J]. FASEB J, 2019, 33(1): 1278-1287.

[17] Yin O, Cayton K, Segars JH. In vitro activation: a dip into the primordial follicle pool[J]? J Clin Endocrinol Metab, 2016, 101(10): 3568-3570.

[18] Lee HN, Chang EM. Primordial follicle activation as new treatment for primary ovarian insufficiency[J]. Clin Exp Reprod Med, 2019, 46(2): 43-49.

[19] Broer SL, Broekmans FJ, Laven JS, et al. AntiMüllerian hormone: ovarian reserve testing and its potential clinical implications[J]. Hum Reprod Update, 2014, 20(5): 688-701.

[20] Polyzos NP, Davis SR, Drakopoulos P, et al. Testosterone for poor ovarian responders: lessons from ovarian physiology[J]. Reprod Sci, 2018, 25(7): 980-982.

基金

黄体生成素对多囊卵巢综合症卵巢缝隙连接蛋白表达调节的研究。;雄激素受体激活Wnt信号通路在胃癌细胞增殖、EMT和侵袭中的研究

PDF(5712 KB)

Accesses

Citation

Detail

段落导航
相关文章

/