Expression Patterns of Key Factors of Wnt/β-catenin and Notch Signaling Pathway in Bovine (Bos taurus) Follicular Granulosa Cells
DANG Wen-Qing1, HE Min1, QU Yu-Han1, ZHANG Kai1, YANG Xiao-Feng2, QIN Xiao-Wei3, HAN Qi1, GUO Xiang-Yu1, LYU Li-Hua1,*
1 College of Animal Science, Shanxi Agricultural University, Taigu 030801, China; 2 Department of Biology, Xinzhou Normal College, Xinzhou 034000, China; 3 Department of Reproductive Medicine, Shanxi Provincial People's Hospital, Taiyuan 030012, China
Abstract:The proliferation, apoptosis and steroid hormone synthesis of granulosa cells play important roles in follicle development, and these functions are regulated by signaling pathways. In this study, the transcriptome sequencing of granulosa cells from the first large follicle F1 and the second large follicle F2 in bovine (Bos taurus) first follicle wave pre-deviation (PD) and onset of diameter deviation (OD) were separately performed to obtain the expression patterns of genes in Wnt/β-catenin and Notch signaling pathways, cell cycle, apoptosis and steroid hormone synthesis, and to validate the expression of key components of the 2 pathways. The results showed that the genes of key components of the 2 pathways with high expression in PDF1, PDF2, ODF1 and ODF2 follicular granulosa cells were wingless-type MMTV integration site family, member 10a (Wnt10a), Wnt2b, frizzled3 (Fzd3), low density lipoprotein-related receptor 8 (LRP8), dishevelled 3 (Dvl3), Axin1, glycogen synthase 3β (GSK3β), catenin beta 1 (CTNNB1), transcription factor 7-like 2 (TCF7L2), lymphoid enhancer factor1 (LEF1), B-cell CLL/Lymphoma 9 (BCL9), Notch2, Dll4 and Hes related with YRPW motif2 (Hey2). Cell cycle-related genes with high expression were cyclin2 (CCND2), cyclindependent kinase4 (CDK4), cyclin-dependent kinase inhibitor 1A (CDKN1A), CDKN1B. The apoptosis of granulosa cells was mainly regulated by BCL2-associated X (Bax) in the mitochondrial apoptosis pathway and executed by Caspase3 and Caspase6. The expression of the steroid genes were 3β-hydroxysteroid dehydrogenase (3β-HSD), cytochrome P450 family 11 subfamily A member 1 (CYP11A1), and CYP19A1 were elevated, and E2 synthesis ability of OD follicular granulosa cells was increased compared with that of PD follicles. Wnt2 protein was localized in follicular granulosa cells in deviation process and its expression was significantly higher in OD follicular granulosa cells (P<0.05); Wnt2b protein was localized in follicular granulosa cells and theca cells and its expression was extremely significant lower in OD follicular granulosa cells (P<0.01). The mRNA expression of CTNNB1, LEF1, Notch2 and Hey2 were all extremely significantly increased in OD follicular granulosa cells (P<0.01). This study showed that the gene expression in F1 and F2 follicular granulosa cells during the deviation of bovine first follicular wave was specific, and the gene expression of key components in Wnt/β-catenin and Notch signaling pathway had the same trend, which provides a reference basis for the molecular regulatory mechanism of granulosa cell function during follicular development.
[1] 陈建伟. 2015. Notch2基因在绵羊卵巢表达的研究[D]. 硕士学位论文, 山西农业大学, 导师: 吕丽华, pp. 25-34. (Chen J W.2015. Study on Notch2 gene expression in sheep ovaries[D]. Thesis for M.S., Shanxi Agriculture University, Supervisor: Lv L H, pp. 25-34.) [2] 孟金柱. 2014. 牛卵泡发育相关基因表达的研究. 硕士学位论文, 山西农业大学,导师: 吕丽华, pp. 10-12. (Meng J Z.2014. Research of genes expression may associate with bovine follicular development[D]. Thesis for M.S., Shanxi Agriculture University, Supervisor: Lv L H, pp. 10-12.) [3] 薛丽娜, 毕锡麟, 王锴, 等. 2020. Wnt2在绵羊卵泡颗粒细胞的表达及功能研究[J]. 畜牧兽医学报, 51(01): 74-82. (Xue L N, Bi X L, Wang K, et al.2020. Expression and function analysis of wnt2 in ovine follicular granulosa cells[J]. ActaVeterinaria et ZootechnicaSinica, 51(01): 74-82.) [4] Abedini A, Zamberlam G, Boerboom D, et al.2015. Non-canonical WNT5A is a potential regulator of granulosa cell function in cattle[J]. Molecular Cellular Endocrinology, 403: 39-45. [5] Adams G P, Matteri R L, Kastelic J P, et al.1992. Association between surges of follicle-stimulating hormone and the emergence of follicular waves in heifers[J]. Reproduction and Fertility, 94(1): 177-188. [6] Ashry M, Folger J K, Rajput S K, et al.2022. FSH stimulated bovine granulosa cell steroidogenesis involves both canonical and noncanonical WNT signaling[J]. Domestic Animal Endocrinology, 78: 106678. [7] Bonds J, Pollan-White S, L Xiang, et al.2014. Is there a link between ovarian cancer and tooth agenesis?[J]. European Journal of Medicine Genetics, 5: 235-239. [8] Castañon B I, Gifford C A.2012. Follicle-stimulating hormone regulation of estradiol production: Possible involvement of WNT2 and β-catenin in bovine granulosa cells[J]. Animal Science, 90(11): 3789-3797. [9] Dang W Q, Ren Y P, Chen Q Q, et al.2024. Notch2 regulates the function of bovine follicular granulosa cells via the Wnt2/β-catenin signaling pathway[J]. Animals, 14(7):1001. [10] Davidson G.2021. LRPs in Wnt Signalling[J]. Handbook of Experimental Pharmacology, 269: 45-73. [11] Ginther O J, Kot K, Kulick L J, et al.1997. Emergence and deviation of follicles during the development of follicular waves in cattle[J]. Theriogenology, 48(1): 75-87. [12] Ginther O J.2000. Selection of the dominant follicle in cattle and horses[J]. Animal Reproduction Science, 60-61: 61-79. [13] Ginther O J.2001. Effect of LH on circulating oestradiol and follicular fluid factor concentrations during follicle deviation in cattle[J]. Reproduction (Cambridge, England), 122(1): 103-110. [14] Guo M, Zhang H, Bian F, et al.2012. P4 down-regulates Jagged2 and Notch1 expression during primordial folliculogenesis[J]. Frontiers in Bioscience (Elite Edition), 4(8): 2631-2644. [15] Gupta P S, Folger J K, Rajput S K, et al.2014. Regulation and regulatory role of WNT signaling in potentiating FSH action during bovine dominant follicle selection[J]. PLOS ONE, 9(6): e100201. [16] Hernandez Gifford J A.2015. The role of Wnt signaling in adult ovarian folliculogenesis[J]. Reproduction, 150(4): R137-148. [17] Ireland J J, Murphee R L, Coulson P B.1980. Accuracy of predicting stages of bovine estrous cycle by gross appearance of the corpus luteum[J]. Dairy Science, 63(1): 155-160. [18] Ireland J J, Roche J F.1983. Development of nonovulatory antral follicles in heifers: Changes in steroids in follicular fluid and receptors for gonadotropins[J]. Endocrinology, 112(1): 150-156. [19] Karin-Kujundzic V, Kardum V, Sola I M, et al.2020. Dishevelled family proteins in serous ovarian carcinomas: A clinicopathologic and molecular study[J]. Acta Pathologica, Microbiologica, et Immunologica Scandinavica, 128(3): 201-210. [20] Lapointe E, Boyer C, Rico C, et al.2012. FZD1 regulates cumulus expansion genes and is required for normal female fertility in mice[J]. Biology of Reproduction, 87(5): 104. [21] Li Y, Jing J, Dang W, et al.2021. Effects of Notch2 on proliferation, apoptosis and steroidogenesis in bovine luteinized granulosa cells[J]. Theriogenology, 171: 55-63. [22] Li Z, Xu Z, Duan C, et al.2018. Role of TCF/LEF transcription factors in bone development and osteogenesis[J]. International Journal of Medical Sciences, 15(12): 1415-1422. [23] Ma L, Zheng Y, Tang X, et al.2019. miR-21-3p inhibits autophagy of bovine granulosa cells by targeting VEGFA via PI3K/AKT signaling[J]. Reproduction, 158(5): 441-452. [24] Masuko K, Masaru K.2020. Precision medicine for human cancers with Notch signaling dysregulation (Review)[J]. International Journal of Molecular Medicine, 45(2): 279-297. [25] Mazzoni S M, Fearon E R.2014. Axin1 and Axin2 variants in gastrointestinal cancers[J]. Cancer Letters, 355(1): 1-8. [26] Meng L, Jan S Z, Hamer G, et al.2018. Preantral follicular atresia occurs mainly through autophagy, while antral follicles degenerate mostly through apoptosis[J]. Biology of Reproduction, 99(4): 853-863. [27] Mikheil D M, Prabhakar K, Arshad A, et al.2019. Notch signaling activation induces cell death in MAPKi‐resistant melanoma cells[J]. Pigment Cell & Melanoma Research, 32(4): 528-539. [28] Miura R.2019. Physiological characteristics and effects on fertility of the first follicular wave dominant follicle in cattle[J]. Reproduction and Development, 65(4): 289-295. [29] Pagie S, Gérard N, Charreau B.2018. Notch signaling triggered via the ligand DLL4 impedes M2 macrophage differentiation and promotes their apoptosis[J]. Cell Communication & Signaling, 16(1): 4. [30] Rajakoski E.1960. The ovarian follicular system in sexually mature heifers with special reference to seasonal, cyclical, end left-right variations[J]. Actaendocrinologica. Supplementum, 34(Suppl 52): 1-68. [31] Riaz H, Yousuf M R, Liang A, et al.2019. Effect of melatonin on regulation of apoptosis and steroidogenesis in cultured buffalo granulosa cells[J]. Animal Science Journal, 90(4): 473-480. [32] Roslan Z, Muhamad M, Selvaratnam L, et al.2019. The roles of low-density lipoprotein receptor-related proteins 5, 6, and 8 in cancer: A review[J]. Oncology, 2019: 4536302. [33] Tepekoy F, Akkoyunlu G.2020. The interaction of Wnt signaling members with growth factors in cultured granulosa cells[J]. Animal Reproduction, 17(2): e20190106. [34] Tepekoy F, Uysal F, Acar N, et al.2019. The effect of GnRH antagonist cetrorelix on Wnt signaling members in pubertal and adult mouse ovaries[J]. Histochemistry and Cell Biology, 152(6): 423-437. [35] Terauchi K J, Shigeta Y, Iguchi T, et al.2016. Role of Notch signaling in granulosa cell proliferation and polyovular follicle induction during folliculogenesis in mouse ovary[J]. Cell and Tissue Research, 365(1): 197-208. [36] Thorvaldsen T E, Pedersenk N M, Wenzel E A-O, et al.2017. Differential roles of AXIN1 and AXIN2 in tankyrase inhibitor-induced formation of degradasomes and β-catenin degradation[J]. PLOS ONE, 12(1): e0170508. [37] Turathum B, Gao E M, Chian R C.2021. The function of cumulus cells in oocyte growth and maturation and in subsequent ovulation and fertilization[J]. Cells, 10(9): 2292. [38] Wang M, Li Y, Molenaar A, et al.2021. Vitamin E and selenium supplementation synergistically alleviate the injury induced by hydrogen peroxide in bovine granulosa cells[J]. Theriogenology, 170: 91-106. [39] Yao X, Wang Z, El-Samahy M A, et al.2020. Roles of vitamin D and its receptor in the proliferation and apoptosis of luteinized granulosa cells in the goat[J]. Reproduction[J]. Fertility and Development, 32(3): 335-348. [40] Zhang J, Zhang X, Zhang L, et al.2012. LRP8 mediates Wnt/beta-catenin signaling and controls osteoblast differentiation[J]. Journal of Bone and Mineral Research, 27(10): 2065-2074. [41] Zheng Y, Ma L, Liu N, et al.2019. Autophagy and apoptosis of porcine ovarian granulosa cells during follicular development[J]. Animals (Basel), 9(12): 1111.