Volume 16, Issue 2 (February 2018)                   IJRM 2018, 16(2): 69-76 | Back to browse issues page


XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Zavareh S, Gholizadeh Z, Lashkarbolouki T. Evaluation of changes in the expression of Wnt/β-catenin target genes in mouse reproductive tissues during estrous cycle: An experimental study. IJRM 2018; 16 (2) :69-76
URL: http://ijrm.ir/article-1-966-en.html
1- School of Biology, Damghan University, Damghan, Iran , Zavareh.S@du.ac.ir
2- School of Biology, Damghan University, Damghan, Iran
Abstract:   (2885 Views)
Background: The Wingless-type (Wnt)/β-catenin signaling pathway controls cell homeostasis. Reproductive tissues are dynamic in response to steroidal hormone changes. Steroidal hormones are known to control the Wnt/β-catenin pathway, but their role in reproductive tissues remains unknown.
Objective: The present study aims to investigate the expression patterns of Wnt/β-catenin target genes in mouse reproductive tissues during the normal estrous cycle.
Materials and Methods: In this experimental study, 16 adult NMRI mice were grouped as proestrus, estrus, metestrus, and diestrus according to vaginal smear and histological evaluation of uterine and ovarian tissues. Uterine horns and ovarian tissues were collected. Reverse transcription quantitative polymerase chain reaction was performed to evaluate the expression of Wnt/β-catenin target genes (Myc2, Ppard, Id2, Birc5, and Ascl2) at different stages of the estrous cycle.
Results: The expression levels of Id2, Ascl2, and Pprd in uterine tissue were significantly higher at the proestrus phase than at the other stages. Meanwhile, Birc5 expression in uterine tissue was significantly higher at the metestrus stage than at the other stages. Furthermore, Myc2 expression was significantly higher at the diestrus stage than at the estrus and metestrus stages. In the ovarian tissue, the highest expression of Id2, Ascl2, and Birc5 was detected at the proestrus stage, whereas the highest expression of Myc2 and Ppard was observed at the estrus stage.
Conclusion: This study showed that Wnt/β-catenin target genes profiles are different among estrous cycle. It seems that different hormonal profiles during estrous cycles play a key role in the expression pattern of Wnt/β-catenin target genes in ovarian and uterine tissue.
Full-Text [PDF 924 kb]   (758 Downloads) |   |   Full-Text (HTML)  (748 Views)  
Type of Study: Original Article |

References
1. Wood GA, Fata JE, Watson KL, Khokha R. Circulating hormones and estrous stage predict cellular and stromal remodeling in murine uterus. Reproduction 2007; 133: 1035-1044. [DOI:10.1530/REP-06-0302]
2. Heffner LJ, Schust DJ. The reproductive system at a glance: 4th John Wiley & Sons; 2010.
3. Hou X, Tan Y, Li M, Dey SK, Das SK. Canonical Wnt signaling is critical to estrogen-mediated uterine growth. Mol Endocrinol 2004; 18: 3035-3049. [DOI:10.1210/me.2004-0259]
4. Tulac S, Nayak NR, Kao LC, Van Waes M, Huang J, Lobo S, et al. Identification, characterization, and regulation of the canonical Wnt signaling pathway in human endometrium. J Clin Endocrinol Metab 2003; 88: 3860-3866. [DOI:10.1210/jc.2003-030494]
5. Katayama S, Ashizawa K, Fukuhara T, Hiroyasu M, Tsuzuki Y, Tatemoto H, et al. Differential expression patterns of Wnt and β-catenin/TCF target genes in the uterus of immature female rats exposed to 17α-ethynyl estradiol. Toxicol Sci 2006; 91: 419-430. [DOI:10.1093/toxsci/kfj167]
6. Cadigan KM, Nusse R. Wnt signaling: a common theme in animal development. Genes Dev 1997; 11: 3286-3305. [DOI:10.1101/gad.11.24.3286]
7. Herbst A, Jurinovic V, Krebs S, Thieme SE, Blum H, Göke B, et al. Comprehensive analysis of β-catenin target genes in colorectal carcinoma cell lines with deregulated Wnt/β-catenin signaling. BMC Genomics 2014; 15: 74. [DOI:10.1186/1471-2164-15-74]
8. Bui TD, Zhang L, Rees MC, Bicknell R, Harris AL. Expression and hormone regulation of Wnt2, 3, 4, 5a, 7a, 7b and 10b in normal human endometrium and endometrial carcinoma. Br J Cancer 1997; 75: 1131-1136. [DOI:10.1038/bjc.1997.195]
9. Miller C, Sassoon DA. Wnt-7a maintains appropriate uterine patterning during the development of the
10. 76 International Journal of Reproductive BioMedicine Vol. 16. No. 2. pp: 69-76, February 2018 mouse female reproductive tract. Development 1998; 125: 3201-3211.
11. Choobineh K, Zavareh S, Salehnia M, Ghorbanian MT, Paylakhi SH. Expression of pluripotent stem cell markers in mouse uterine tissue during estrous cycle. Vet Res Forum 2016; 7: 181-188.
12. Bagheripour N, Zavareh S, Ghorbanian MT, Paylakhi SH, Mohebbi SR. Changes in the expression of OCT4 in mouse ovary during estrous cycle. Vet Res Forum 2017; 8: 43-48.
13. Couse JF, Korach KS. Estrogen receptor null mice: what have we learned and where will they lead us? Endocr Rev 1999; 20: 358-417. [DOI:10.1210/edrv.20.3.0370]
14. Mericskay M, Kitajewski J, Sassoon D. Wnt5a is required for proper epithelial-mesenchymal interactions in the uterus. Development 2004; 131: 2061-2072. [DOI:10.1242/dev.01090]
15. Miller C, Pavlova A, Sassoon DA. Differential expression patterns of Wnt genes in the murine female reproductive tract during development and the estrous cycle. Mech Dev 1998; 76: 91-99. [DOI:10.1016/S0925-4773(98)00112-9]
16. Wood GA, Fata JE, Watson KL, Khokha R. Circulating hormones and estrous stage predict cellular and stromal remodeling in murine uterus. Reproduction 2007; 133: 1035-1044. [DOI:10.1530/REP-06-0302]
17. O'Connor DS, Wall NR, Porter AC, Altieri DC. A p34 (cdc2) survival checkpoint in cancer. Cancer Cell 2002; 2: 43-54. [DOI:10.1016/S1535-6108(02)00084-3]
18. Peddada S, Yasui DH, LaSalle JM. Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome. Hum Mol Genet 2006; 15: 2003-2014. [DOI:10.1093/hmg/ddl124]
19. Park HJ, Hong M, Bronson RT, Israel MA, Frankel WN, Yun K. Elevated Id2 expression results in precocious neural stem cell depletion and abnormal brain development. Stem Cells 2013; 31: 1010-1021. [DOI:10.1002/stem.1351]
20. Schuhmacher M, Staege MS, Pajic A, Polack A, Weidle UH, Bornkamm GW, et al. Control of cell growth by c-Myc in the absence of cell division. Curr Biol 1999; 9: 1255-1258. [DOI:10.1016/S0960-9822(99)80507-7]
21. Wilson A, Murphy MJ, Oskarsson T, Kaloulis K, Bettess MD, Oser GM, et al. c-Myc controls the balance between hematopoietic stem cell self-renewal and differentiation. Genes Dev 2004; 18: 2747-2763. [DOI:10.1101/gad.313104]
22. Li F, Ambrosini G, Chu EY, Plescia J, Tognin S, Marchisio PC, et al. Control of apoptosis and mitotic spindle checkpoint by survivin. Nature 1998; 396: 580-584. [DOI:10.1038/25141]
23. Hsieh M, Johnson MA, Greenberg NM , Richards JS. Regulated expression of Wnts and Frizzleds at specific stages of follicular development in the rodent ovary. Endocrinology 2002; 143: 898-908. [DOI:10.1210/endo.143.3.8684]
24. Harwood BN, Cross SK, Radford EE, Haac BE, De Vries WN. Members of the WNT signaling pathways are widely expressed in mouse ovaries, oocytes, and cleavage stage embryos. Dev Dyn 2008; 237: 1099-111. [DOI:10.1002/dvdy.21491]
25. Wang Y, Hanifi-Moghaddam P, Hanekamp EE, Kloosterboer HJ, Franken P, Veldscholte J, et al. Progesterone inhibition of Wnt/β-catenin signaling in normal endometrium and endometrial cancer. Clin Cancer Res 2009; 15: 5784-5793. [DOI:10.1158/1078-0432.CCR-09-0814]
26. Casta-on BI, Stapp AD, Gifford CA, Spicer LJ, Hallford DM, Hernandez Gifford JA. Follicle-stimulating hormone regulation of estradiol production: possible involvement of WNT2 and β-catenin in bovine granulosa cells. J Anim Sci 2012; 90: 3789-3797. [DOI:10.2527/jas.2011-4696]
27. Gupta PS, Folger JK, Rajput SK, Lv L, Yao J, Ireland JJ, et al. Regulation and regulatory role of WNT signaling in potentiating FSH action during bovine dominant follicle selection. PloS One 2014; 9: e100201. [DOI:10.1371/journal.pone.0100201]
28. Stapp AD, Gómez BI, Gifford CA, Hallford DM, Hernandez Gifford JA. Canonical WNT signaling inhibits follicle stimulating hormone mediated steroidogenesis in primary cultures of rat granulosa cells. PloS One 2014; 9: e86432. [DOI:10.1371/journal.pone.0086432]
29. Fan HY, O'connor A, Shitanaka M, Shimada M, Liu Z, Richards JS. Beta-Catenin (CTNNB1) promotes preovulatory follicular development but represses LH-mediated ovulation and luteinization. Mol Endocrinol 2010; 24: 1529-1542. [DOI:10.1210/me.2010-0141]
30. Law NC, Weck J, Kyriss B, Nilson JH, Hunzicker-Dunn M. Lhcgr expression in granulosa cells: roles for PKA-phosphorylated β-catenin, TCF3, and FOXO1. Mol Endocrinol 2013; 27: 1295-1310. [DOI:10.1210/me.2013-1025]

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Designed & Developed by : Yektaweb