Effect of Estradiol on Granulosa Cells of Goose (Anser cygnoides domestica) Grade Follicles
SU Hang, LAN Gang, HU Shen-Qiang, OUYANG Qing-Yuan, GAN Xiang, CHEN Xi, WANG Ji-Wen*
Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China
Abstract:Estradiol (E2) plays an important role in regulating the growth and development of granulosa cells.To explore the effect of estradiol (E2) at different concentrations on Goose (Anser cygnoides domestica) hierarchical follicular granulosa cells (HFGCs) and its molecular mechanism, in this study, the grade granulosa cells of 'Tianfu' geese were randomly divided into experimental group (E5, E7, E9) and control group (NC), the granulosa cells of experimental group were treated with different concentrations of estradiol (1×10-5, 1×10-7 and 1×10-9 mol/L). The samples were collected for MTT assay, oil staining assay and transcriptome sequencing analysis. MTT results showed that the cell activity of the experimental group was significantly higher than that of the control group (P<0.05); Oil red staining results showed that with the decrease of E2 concentration, the lipid deposition of granulosa cells decreased, and the difference was significant when E2 concentration was 1×10-9 mol/L (P<0.05); By transcriptome sequencing analysis, E5, E7, E9 were compared with NC under the condition of fold change (FC)>1.2 or <0.83 and P<0.05, 267, 79 and 162 differentially expressed genes were screened, respectively; KEGG enrichment analysis showed that the differentially expressed genes of E5, E7, E9 and NC were significantly enriched in sphingolipid metabolism, insulin signaling and Wnt signaling, ABC transporter and other pathways, respectively. 3-ketodihydrosphingosine reductase (KDSR), ceramide synthase 6 (CERS6) and ceramide synthase 4 (CERS4) in sphingolipid metabolism pathway, mitogen-activated protein kinase 8 (MAPK8), inositol polyphosphate phosphatase like 1 (INPPL) and sclerostin (SOST) in insulin and Wnt signaling pathway were involved in regulating granulocyte activity; Galactose-3-O-sulfotransferase 1 (GAL3ST1), sphingosine-1-phosphate lyase 1 (SGPL1), ATP binding cassette subfamily A member 2 (ABCA2) and ATP binding cassette subfamily A member 5 (ABCA5) in sphingolipid metabolism and ABC transporter pathway were involved in regulating granulosa cells lipid deposition when E2 concentration was 1×10-9 mol/L. The results showed that exogenous E2 treatment could improve the activity of goose granulosa cells and inhibit lipid deposition by affecting sphingolipid metabolism, insulin signaling, Wnt signaling and the expression levels of related genes in ABC transporter pathway. The results lay a foundation for exploring the molecular mechanism of estradiol regulating the growth and development of goose granulosa cells.
[1] 赵丹. 2018. 雌激素和TGF-β1对鸡原始卵泡和生长卵泡发育的调节作用及其机理的研究[D]. 博士学位论文, 浙江大学, 导师: 张才乔, pp. 127-129. (Zhao D. 2018. Regulation of estrogen and TGF-β1 on the development of primordial and growing follicles in chickens and its mechanism[D]. Thesis for Ph.D., Zhejiang University, Suppervisor: Zhang C Q, pp. 127-129.) [2] Abiola M, Favier M, Christodoulou-Vafeiadou E, et al.2009. Activation of Wnt/β-catenin signaling increases insulin sensitivity through a reciprocal regulation of Wnt10b and SREBP-1c in skeletal muscle cells[J]. PLOS ONE, 4(12): e8509. [3] Bhukhai K, Suksen K, Bhummaphan N, et al.2012. A phytoestrogen diarylheptanoid mediates estrogen receptor/Akt/glycogen synthase kinase 3β protein-dependent activation of the Wnt/β-catenin signaling pathway[J]. Journal of Biological Chemistry, 287(43): 36168-36178. [4] Billig H, Furuta I, Hsueh A J.1993. Estrogens inhibit and androgens enhance ovarian granulosa cell apoptosis[J]. Endocrinology, 133(5): 2204-2212. [5] Bristol-Gould S K, Kreeger P K, Selkirk C G, et al.2006. Postnatal regulation of germ cells by activin: The establishment of the initial follicle pool[J]. Developmental Biology, 298(1): 132-148. [6] Casarini L, Laura R, Francesco D P, et al.2017. Estrogen modulates specific life and death signals induced by LH and hCG in human primary granulosa cells in vitro[J]. International Journal of Molecular Sciences, 18(5): 926. [7] Choi Y J, Saba J D.2019. Sphingosine phosphate lyase insufficiency syndrome (SPLIS): A novel inborn error of sphingolipid metabolism[J]. Advances in Biological Regulation, 71: 128-140. [8] Davis A J, Brooks C F, Johnson P A.2000. Estradiol regulation of follistatin and inhibin alpha- and beta(B)-subunit mRNA in avian granulosa cells[J]. General and Comparative Eendocrinology, 119(3): 308-316. [9] Eppig J J.2001. Oocyte control of ovarian follicular development and function in mammals[J]. Reproduction, 122(6): 829-838. [10] Hoogeboom D, Essers M A, Polderman P E, et al.2008. Interaction of FOXO with beta-catenin inhibits beta-catenin/T cell factor activity[J]. Journal of Biological Chemistry, 283(14): 9224-9230. [11] Hrabia A, Wilk M, Rzasa J.2008. Expression of alpha and beta estrogen receptors in the chicken ovary[J]. Folia Biologica (Krakow), 56(3-4): 187-191. [12] Johnson A L, Bridgham J T, Swenson J A.2001. Activation of the Akt/protein kinase B signaling pathway is associated with granulosa cell survival[J]. Biology of Reproduction, 64(5): 1566-1574. [13] Jones E, Mead S.2020. Genetic risk factors for Creutzfeldt-Jakob disease[J]. Neurobiology of Disease, 142: 104973. [14] Kim R Y, Yang H J, Song Y M, et al.2015. Estrogen modulates BMP-induced sclerostin expression via the Wnt signaling pathway[J]. Tissue Engineering Part A, 21(13-14): 2076-2088. [15] Kohama T, Olivera A, Edsall L, et al.1998. Molecular cloning and functional characterization of murine sphingosine kinase[J]. Journal of Biological Chemistry, 273(37): 23722-23728. [16] Lovell T M, Gladwell R T, Groome N P, et al.2003. Ovarian follicle development in the laying hen is accompanied by divergent changes in inhibin A, inhibin B, activin A and follistatin production in granulosa and theca layers[J]. The Journal of Endocrinology, 177(1): 45-55. [17] Lee H T, Bahr J M.1989. Inhibitory sites of androgens and estradiol in progesterone biosynthesis in granulosa cells of the domestic hen[J]. Endocrinology, 125(2): 760-765. [18] Martins da Silva S J, Bayne R A, Cambray N, et al.2004. Expression of activin subunits and receptors in the developing human ovary: Activin A promotes germ cell survival and proliferation before primordial follicle formation[J].Developmental Biology, 266(2): 334-345. [19] Mbalaviele G, Sheikh S, Stains J P, et al.2010. Beta-catenin and BMP-2 synergize to promote osteoblast differentiation and new bone formation[J]. Journal of Cellular Biochemistry, 94(2): 403-418. [20] McGee E A, Hsueh A J.2000. Initial and cyclic recruitment of ovarian follicles[J]. Endocrine Reviews, 21(2): 200-214. [21] Mitroi D N, Karunakaran I, Gräler M, et al.2017. SGPL1 (sphingosine phosphate lyase 1) modulates neuronal autophagy via phosphatidylethanolamine production[J].Autophagy, 13(5): 885-899. [22] Onagbesan O, Bruggeman V, Decuypere E.2009. Intra-ovarian growth factors regulating ovarian function in avian species: A review[J]. Animal Reproduction Science, 111(2-4): 121-140. [23] Schmitz G, Kaminski W E.2002. ABCA2: A candidate regulator of neural transmembrane lipid transport[J]. Cellular and Molecular Life Sciences, 59(8): 1285-1295. [24] Thomas F H,Vanderhyden B C.2006. Oocyte-granulosa cell interactions during mouse follicular development: Regulation of kit ligand expression and its role in oocyte growth[J]. Reproductive Biology and Endocrinology, 4: 19. [25] Turner I M, Saunders P T, Shimasaki S, et al.1989. Regulation of inhibin subunit gene expression by FSH and estradiol in cultured rat granulosa cells[J]. Endocrinology, 125(5): 2790-2792. [26] Wang Y, Bi Y, Zuo Q, et al.2018. MAPK8 regulates chicken male germ cell differentiation through JNK signaling pathway[J]. Journal of Cellular Biochemistry, 119(2): 1548-1557. [27] Ye D, Meurs I, Ohigashi M,et al.2010. Macrophage ABCA5 deficiency influences cellular cholesterol efflux and increases susceptibility to atherosclerosis in female LDLr knockout mice[J]. Biochemical and Biophysical Research Communications, 395(3): 387-394.