Register      Login
Reproduction, Fertility and Development Reproduction, Fertility and Development Society
Vertebrate reproductive science and technology
RESEARCH ARTICLE

Regulation by 3,5,3′-tri-iodothyronine and FSH of cytochrome P450 family 19 (CYP19) expression in mouse granulosa cells

Juan Liu A D , Yingying Han B , Ye Tian A , Xuechun Weng A , Xusong Hu A , Wenbo Liu A , Dai Heng A , Kaili Xu A , Yanzhou Yang C E and Cheng Zhang A E
+ Author Affiliations
- Author Affiliations

A College of Life Science, Capital Normal University, Beijing 100048, P.R. China.

B College of Biological Sciences and Biotechnology, Beijing Forestry University, Beijing 100083, P.R. China.

C Key Laboratory of Fertility Preservation and Maintenance, Ministry of Education, Key Laboratory of Reproduction and Genetics in Ningxia, Department of Histology and Embryology, Ningxia Medical University, Ningxia 750004, P.R. China.

D State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, P.R. China.

E Corresponding author. Email: zhch8012@163.com

Reproduction, Fertility and Development 30(9) 1225-1233 https://doi.org/10.1071/RD17362
Submitted: 10 September 2017  Accepted: 26 February 2018   Published: 9 April 2018

Abstract

Cytochrome P450 family 19 (CYP19) plays an important role in follicular development, which is regulated by FSH. Although 3,5,3′-tri-iodothyronine (T3) combines with FSH to induce preantral follicle growth and granulosa cell development, the mechanism involved remains unclear. The aim of the present study was to determine the cellular and molecular mechanisms by which thyroid hormone (TH) and FSH regulate CYP19 expression and sterol biosynthesis during preantral follicle growth. Mice were injected subcutaneously (s.c.) with eCG (Equine chorionic gonadotropin). The results showed that eCG increased CYP19 expression in ovarian cells. CYP19 expression in granulosa cells was increased after FSH treatment, and this response was enhanced by T3. Knockdown of CYP19 significantly decreased granulosa cell viability and hormone-stimulated proliferation. In addition, CYP19 knockdown also blocked T3- and FSH-induced oestradiol (E2) synthesis in granulosa cells. Furthermore, activation of the phosphatidylinositol 3-kinase (PI3K)/Akt pathway was required for T3 and FSH regulation of CYP19 expression. In conclusion, the results of the present study indicate that CYP19 is important for T3- and FSH-induced granulosa cell development in the early stages. CYP19 could be a downstream effector of the PI3K/Akt pathway in regulating TH and FSH during follicular development and sterol biosynthesis. The findings suggest that CYP19 is a novel mediator of T3- and FSH-induced follicular development.

Additional keywords: steroid hormone.


References

Asselin, E., Wang, Y., and Tsang, B. K. (2001). X-Linked inhibitor of apoptosis protein activates the phosphatidylinositol 3-kinase/Akt pathway in rat granulosa cells during follicular development. Endocrinology 142, 2451–2457.
X-Linked inhibitor of apoptosis protein activates the phosphatidylinositol 3-kinase/Akt pathway in rat granulosa cells during follicular development.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXjvFGns78%3D&md5=3522827086634864eba49b14b51baca7CAS |

Baird, D. (2006). Role of FSH and LH in follicle development. J. Gynecol. Obstet. Biol. Reprod. (Paris) 35, 2S24–2S29.
| 1:STN:280:DC%2BD28nitlGqsQ%3D%3D&md5=a01b72d5419bc8c5ea65b89d75cfbd36CAS |

Chen, Y., Liu, Q., Wu, M., Li, M., Ding, H., Shan, X., Liu, J., Tao, T., Ni, R., and Chen, X. (2016). GAB2 promotes cell proliferation by activating the ERK signaling pathway in hepatocellular carcinoma. Tumour Biol. 37, 11763–11773.
GAB2 promotes cell proliferation by activating the ERK signaling pathway in hepatocellular carcinoma.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC28XlsVOms70%3D&md5=4612672867922ba6ed3777f1cb808710CAS |

Ding, Y., Tian, Y., Guo, M., Liu, J., Heng, D., Zhu, B., Yang, Y., and Zhang, C. (2016). Regulation of glucose transport by thyroid hormone in rat ovary. Cell Tissue Res. 366, 455–466.
Regulation of glucose transport by thyroid hormone in rat ovary.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC28XhtFOlsr3N&md5=ae1dff54c601bb8e56c0da8990f567e2CAS |

Donadeu, F. X., and Pedersen, H. G. (2008). Follicle development in mares. Reprod. Domest. Anim. 43, 224–231.
Follicle development in mares.Crossref | GoogleScholarGoogle Scholar |

Fedail, J. S., Zheng, K., Wei, Q., Kong, L., and Shi, F. (2014). Roles of thyroid hormones in follicular development in the ovary of neonatal and immature rats. Endocrine 46, 594–604.
Roles of thyroid hormones in follicular development in the ovary of neonatal and immature rats.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXhsl2murzI&md5=3906160005fe7319859ac0e91ed04009CAS |

Hunter, M. G., and Paradis, F. (2009). Intra-follicular regulatory mechanisms in the porcine ovary. Soc. Reprod. Fertil. Suppl. 66, 149–164.
| 1:CAS:528:DC%2BC3cXjslKjtLg%3D&md5=c4fbe159764050ee0c41e41a642ffbefCAS |

Jiang, J. Y., Miyoshi, K., Umezu, M., and Sato, E. (1999). Superovulation of immature hypothyroid RDW rats by thyroxine therapy and the development of eggs after in vitro fertilization. J. Reprod. Fertil. 116, 19–24.
Superovulation of immature hypothyroid RDW rats by thyroxine therapy and the development of eggs after in vitro fertilization.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXjvVemsLo%3D&md5=3734c28a8e85eeb8117215cbe8e9c71bCAS |

Jiang, J. Y., Umezu, M., and Sato, E. (2000). Improvement of follicular development rather than gonadotrophin secretion by thyroxine treatment in infertile immature hypothyroid RDW rats. J. Reprod. Fertil. 119, 193–199.
| 1:CAS:528:DC%2BD3cXltlylsbo%3D&md5=a02f1d747f9a930ba671aadb3d388917CAS |

Jiang, J. Y., Cheung, C. K., Wang, Y., and Tsang, B. K. (2003). Regulation of cell death and cell survival gene expression during ovarian follicular development and atresia. Front. Biosci. 8, D222–D237.
Regulation of cell death and cell survival gene expression during ovarian follicular development and atresia.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXhsVejs74%3D&md5=367bd2026ff5f24af83fc7a92b8dd41fCAS |

Kwintkiewicz, J., Cai, Z., and Stocco, C. (2007). Follicle-stimulating hormone-induced activation of Gata4 contributes in the up-regulation of Cyp19 expression in rat granulosa cells. Mol. Endocrinol. 21, 933–947.
Follicle-stimulating hormone-induced activation of Gata4 contributes in the up-regulation of Cyp19 expression in rat granulosa cells.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXksFWhtrY%3D&md5=cfaa974ad40d589a445e2e4a7b87da7eCAS |

Liu, J., Tian, Y., Ding, Y., Heng, D., Xu, K., Liu, W., and Zhang, C. (2017). Role of CYP51 in the regulation of T3 and FSH-induced steroidogenesis in female mice. Endocrinology 158, 3974–3987.
Role of CYP51 in the regulation of T3 and FSH-induced steroidogenesis in female mice.Crossref | GoogleScholarGoogle Scholar |

Livak, K. J., and Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2(−Delta Delta C(T)) method. Methods 25, 402–408.
Analysis of relative gene expression data using real-time quantitative PCR and the 2(−Delta Delta C(T)) method.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XhtFelt7s%3D&md5=a80b5e0841c49e736a3564bfe77a7aa6CAS |

Mahendroo, M. S., Mendelson, C. R., and Simpson, E. R. (1993). Tissue-specific and hormonally controlled alternative promoters regulate aromatase cytochrome P450 gene expression in human adipose tissue. J. Biol. Chem. 268, 19463–19470.
| 1:CAS:528:DyaK2cXntVOitA%3D%3D&md5=7a4031d532a6ae1f70b4be56fc8a621fCAS |

Maruo, T., Katayama, K., Barnea, E. R., and Mochizuki, M. (1992). A role for thyroid hormone in the induction of ovulation and corpus luteum function. Horm. Res. 37, 12–18.
A role for thyroid hormone in the induction of ovulation and corpus luteum function.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK38Xks1ensb8%3D&md5=4fcf9abee1e1748f3eb65442b3f6c6f3CAS |

Medenica, S., Nedeljkovic, O., Radojevic, N., Stojkovic, M., Trbojevic, B., and Pajovic, B. (2015). Thyroid dysfunction and thyroid autoimmunity in euthyroid women in achieving fertility. Eur. Rev. Med. Pharmacol. Sci. 19, 977–987.
| 1:STN:280:DC%2BC2Mjis1OhtA%3D%3D&md5=ba343b1b9b3da6e9a6a1497992e6d0f5CAS |

Motola, S., Cao, X., Ashkenazi, H., Popliker, M., and Tsafriri, A. (2006). GnRH actions on rat preovulatory follicles are mediated by paracrine EGF-like factors. Mol. Reprod. Dev. 73, 1271–1276.
GnRH actions on rat preovulatory follicles are mediated by paracrine EGF-like factors.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XptlSnu70%3D&md5=27348bcf1d0e5950e26720095cc19e6dCAS |

Peluso, J. J., and Steger, R. W. (1978). Role of FSH in regulating granulosa cell division and follicular atresia in rats. J. Reprod. Fertil. 54, 275–278.
Role of FSH in regulating granulosa cell division and follicular atresia in rats.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE1MXkvVOnsw%3D%3D&md5=26f1e5efd6799bd48d67f6a0a33716d8CAS |

Quesnel, H. (2009). Nutritional and lactational effects on follicular development in the pig. Soc. Reprod. Fertil. Suppl. 66, 121–134.
| 1:STN:280:DC%2BD1MjgvFamug%3D%3D&md5=28308f46da3a2a6f30738de311745656CAS |

Rao, I. M., Mills, T. M., Anderson, E., and Mahesh, V. B. (1991). Heterogeneity in granulosa cells of developing rat follicles. Anat. Rec. 229, 177–185.
Heterogeneity in granulosa cells of developing rat follicles.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK3M7ovFCqsw%3D%3D&md5=5ee983aa954aed7e340e825dc4e04af8CAS |

Shoham, Z., and Schachter, M. (1996). Estrogen biosynthesis—regulation, action, remote effects, and value of monitoring in ovarian stimulation cycles. Fertil. Steril. 65, 687–701.
Estrogen biosynthesis—regulation, action, remote effects, and value of monitoring in ovarian stimulation cycles.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK283mslSisQ%3D%3D&md5=81fafb5257f2680899bab37e3f346928CAS |

Silva, J. R., Figueiredo, J. R., and van den Hurk, R. (2009). Involvement of growth hormone (GH) and insulin-like growth factor (IGF) system in ovarian folliculogenesis. Theriogenology 71, 1193–1208.
Involvement of growth hormone (GH) and insulin-like growth factor (IGF) system in ovarian folliculogenesis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXktF2nur0%3D&md5=4006b562b0f071f06de803033bdbb554CAS |

Tan, W., Zhu, Z., Ye, L., and Leung, L. K. (2017). Methylation dictates PI.f-specific CYP19 transcription in human glial cells. Mol. Cell. Endocrinol. 452, 131–137.
Methylation dictates PI.f-specific CYP19 transcription in human glial cells.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2sXptFClt78%3D&md5=ea3576fd6f4d0c0375cf02b69ea22498CAS |

Tian, Y., Ding, Y., Liu, J., Heng, D., Xu, K., Liu, W., and Zhang, C. (2017). Nitric oxide-mediated regulation of GLUT by T3 and follicle-stimulating hormone in rat granulosa cells. Endocrinology 158, 1898–1915.
Nitric oxide-mediated regulation of GLUT by T3 and follicle-stimulating hormone in rat granulosa cells.Crossref | GoogleScholarGoogle Scholar |

Toda, K., Takeda, K., Okada, T., Akira, S., Saibara, T., Kaname, T., Yamamura, K., Onishi, S., and Shizuta, Y. (2001). Targeted disruption of the aromatase P450 gene (Cyp19) in mice and their ovarian and uterine responses to 17beta-oestradiol. J. Endocrinol. 170, 99–111.
| 1:CAS:528:DC%2BD3MXltlaksr0%3D&md5=ca73674699777b03678cd4e5147586e5CAS |

Wang, Y., Rippstein, P. U., and Tsang, B. K. (2003). Role and gonadotrophic regulation of X-linked inhibitor of apoptosis protein expression during rat ovarian follicular development in vitro. Biol. Reprod. 68, 610–619.
Role and gonadotrophic regulation of X-linked inhibitor of apoptosis protein expression during rat ovarian follicular development in vitro.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXntVChtA%3D%3D&md5=1b3611e1f767f406d9bc1e1168193a3cCAS |

Wang, Q., Kim, J. Y., Xue, K., Liu, J. Y., Leader, A., and Tsang, B. K. (2012). Chemerin, a novel regulator of follicular steroidogenesis and its potential involvement in polycystic ovarian syndrome. Endocrinology 153, 5600–5611.
Chemerin, a novel regulator of follicular steroidogenesis and its potential involvement in polycystic ovarian syndrome.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xhs1Onsb%2FL&md5=e0a426a72fc4535928f7da367025b39cCAS |

Wang, Q., Leader, A., and Tsang, B. K. (2013a). Follicular stage-dependent regulation of apoptosis and steroidogenesis by prohibitin in rat granulosa cells. J. Ovarian Res. 6, 23.
Follicular stage-dependent regulation of apoptosis and steroidogenesis by prohibitin in rat granulosa cells.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXotFCntLg%3D&md5=2b1e90038e271408ca1eb15a7d88f263CAS |

Wang, Q., Leader, A., and Tsang, B. K. (2013b). Inhibitory roles of prohibitin and chemerin in FSH-induced rat granulosa cell steroidogenesis. Endocrinology 154, 956–967.
Inhibitory roles of prohibitin and chemerin in FSH-induced rat granulosa cell steroidogenesis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXitVehtbo%3D&md5=774617c8d2f75705aa2d3771c9cc00e1CAS |

Webb, R., and Campbell, B. K. (2007). Development of the dominant follicle: mechanisms of selection and maintenance of oocyte quality. Soc. Reprod. Fertil. Suppl. 64, 141–163.
| 1:CAS:528:DC%2BD1cXpvVyrs7w%3D&md5=6083a560101c4f993a88de2d968a38ecCAS |

Zhang, H., Xu, B., Xie, H., Zhou, B., Ouyang, H., Ning, G., Li, G., Zhang, M., and Xia, G. (2009). Lanosterol metabolic product(s) is involved in primordial folliculogenesis and establishment of primordial folliclepool in mouse fetal ovary. Mol. Reprod. Dev. 76, 514–521.
Lanosterol metabolic product(s) is involved in primordial folliculogenesis and establishment of primordial folliclepool in mouse fetal ovary.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXktVWjtL4%3D&md5=bce3b04febb3129957b03b41883189bdCAS |

Zhang, C., Xia, G., and Tsang, B. K. (2011). Interactions of thyroid hormone and FSH in the regulation of rat granulosa cell apoptosis. Front. Biosci. (Elite Ed.) 3, 1401–1413.

Zhang, C., Guo, L., Zhu, B., Feng, Y., Yu, S., An, N., and Wang, X. (2013a). Effects of 3,5,3′-triiodothyronine (T3) and follicle stimulating hormone on apoptosis and proliferation of rat ovarian granulosa cells. Chin. J. Physiol. 56, 298–305.
| 1:CAS:528:DC%2BC3sXhvVGrt7zM&md5=19c986d8ac05f9bab6ef05ec5fd15aafCAS |

Zhang, C., Wang, X., Wang, Z., Niu, W., Zhu, B., and Xia, G. (2013b). Effect of different culture systems and 3,5,3′-triiodothyronine/follicle-stimulating hormone on preantral follicle development in mice. PLoS One 8, e61947.
Effect of different culture systems and 3,5,3′-triiodothyronine/follicle-stimulating hormone on preantral follicle development in mice.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXmslSjs78%3D&md5=74b3ce2ba13b163162cabdbe080f9c7aCAS |