The theca interna is a specialized stromal layer that envelops each growing ovarian follicle. It contains capillaries, fibroblasts, immune cells and the steroidogenic cells that synthesize androgens for conversion to estradiol by the neighboring granulosa cells. During reproductive life only a small number of follicles will grow to a sufficient size to ovulate, whereas the majority of follicles will undergo regression/atresia and phagocytosis by macrophages. To identify genes which are differentially regulated in the theca interna during follicular atresia, we undertook transcriptome profiling of the theca interna from healthy (n = 10) and antral atretic (n = 5) bovine follicles at early antral stages (<5 mm). Principal Component Analyses and hierarchical classification of the signal intensity plots for the arrays showed primary clustering into two groups, healthy and atretic. A total of 543 probe sets were differentially expressed between the atretic and healthy theca interna. Further analyses of these genes by Ingenuity Pathway Analysis and Gene Ontology Enrichment Analysis Toolkit software found most of the genes being expressed were related to cytokines, hormones and receptors as well as the cell cycle and DNA replication. Cell cycle genes which encode components of the replicating chromosome complex and mitotic spindle were down-regulated in atretic theca interna, whereas stress response and inflammation-related genes such as TP53, IKBKB and TGFB1 were up-regulated. In addition to cell cycle regulators, upstream regulators that were predicted to be inhibited included Retinoblastoma 1, E2 transcription factor 1, and hepatocyte growth factor. Our study suggests that during antral atresia of small follicles in the theca interna, arrest of cell cycle and DNA replication occurs rather than up- regulation of apoptosis-associated genes as occurs in granulosa cells.
References
[1]
Falck B (1959) Site of production of oestrogen in the ovary of the rat. Nature (Suppl 14): 1082. doi: 10.1038/1841082a0
[2]
Rodgers RJ, Irving-Rodgers HF (2010) Formation of the ovarian follicular antrum and follicular fluid. Biol Reprod 82: 1021–1029. doi: 10.1095/biolreprod.109.082941
[3]
Irving-Rodgers HF, Rodgers RJ (2000) Ultrastructure of the basal lamina of bovine ovarian follicles and its relationship to the membrana granulosa. J Reprod Fertil 118: 221–228. doi: 10.1530/reprod/118.2.221
[4]
Irving-Rodgers HF, Morris S, Collett RA, Peura TT, Davy M, et al. (2009) Phenotypes of the ovarian follicular basal lamina predict developmental competence of oocytes. Hum Reprod 24: 936–944. doi: 10.1093/humrep/den447
Irving-Rodgers HF, van Wezel IL, Mussard ML, Kinder JE, Rodgers RJ (2001) Atresia revisited: two basic patterns of atresia of bovine antral follicles. Reproduction 122: 761–775. doi: 10.1530/rep.0.1220761
[7]
Christenson LK, Gunewardena S, Hong X, Spitschak M, Baufeld A, et al. (2013) Research Resource: Preovulatory LH Surge Effects on Follicular Theca and Granulosa Transcriptomes. Mol Endocrinol 27: 1153–1171. doi: 10.1210/me.2013-1093
[8]
Portela VM, Machado M, Buratini J Jr, Zamberlam G, Amorim RL, et al. (2010) Expression and function of fibroblast growth factor 18 in the ovarian follicle in cattle. Biol Reprod 83: 339–346. doi: 10.1095/biolreprod.110.084277
[9]
Irving-Rodgers HF, Mussard ML, Kinder JE, Rodgers RJ (2002) Composition and morphology of the follicular basal lamina during atresia of bovine antral follicles. Reproduction 123: 97–106. doi: 10.1530/rep.0.1230097
[10]
Irving-Rodgers HF, Krupa M, Rodgers RJ (2003) Cholesterol side-chain cleavage cytochrome P450 and 3beta-hydroxysteroid dehydrogenase expression and the concentrations of steroid hormones in the follicular fluids of different phenotypes of healthy and atretic bovine ovarian follicles. Biol Reprod 69: 2022–2028. doi: 10.1095/biolreprod.103.017442
[11]
Clark LJ, Irving-Rodgers HF, Dharmarajan AM, Rodgers RJ (2004) Theca interna: the other side of bovine follicular atresia. Biol Reprod 71: 1071–1078. doi: 10.1071/srb04abs206
[12]
Irving-Rodgers HF, Catanzariti KD, Master M, Grant PA, Owens PC, et al. (2003) Insulin-like growth factor binding proteins in follicular fluid from morphologically distinct healthy and atretic bovine antral follicles. Reprod Fertil Dev 15: 241–248. doi: 10.1071/rd03008
[13]
Irizarry RA, Hobbs B, Collin F, Beazer-Barclay YD, Antonellis KJ, et al. (2003) Exploration, normalization, and summaries of high density oligonucleotide array probe level data. Biostatistics 4: 249–264. doi: 10.1093/biostatistics/4.2.249
[14]
Bolstad BM, Irizarry RA, Astrand M, Speed TP (2003) A comparison of normalization methods for high density oligonucleotide array data based on variance and bias. Bioinformatics 19: 185–193. doi: 10.1093/bioinformatics/19.2.185
[15]
Hatzirodos N, Hummitzsch K, Irving-Rodgers HF, Rodgers RJ (2014) Transcriptome profiling of the theca interna in transition from small to large antral ovarian follicles. PLoS ONE (submitted). doi: 10.1371/journal.pone.0097489
[16]
Hotelling H (1933) Analysis of a complex of statistical variables into principal components. Journal of Education Psychology 24: 417–441. doi: 10.1037/h0071325
[17]
Eisenhart C (1947) The assumptions underlying the analysis of variance. Biometrics 3: 1–21. doi: 10.2307/3001534
[18]
Barrett T, Troup DB, Wilhite SE, Ledoux P, Rudnev D, et al. (2009) NCBI GEO: archive for high-throughput functional genomic data. Nucleic Acids Res 37: D885–890. doi: 10.1093/nar/gkn764
[19]
Hatzirodos N, Hummitzsch K, Irving-Rodgers HF, Harland ML, Morris SE, et al. (2014) Transcriptome profiling of granulosa cells from bovine ovarian follicles during atresia. BMC Genomics 15: 40. doi: 10.1186/1471-2164-15-40
[20]
Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, et al. (2000) Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet 25: 25–29.
[21]
Zheng Q, Wang XJ (2008) GOEAST: a web-based software toolkit for Gene Ontology enrichment analysis. Nucleic Acids Res 36: W358–363. doi: 10.1093/nar/gkn276
[22]
Prodoehl MJ, Irving-Rodgers HF, Bonner WM, Sullivan TM, Micke GC, et al. (2009) Fibrillins and latent TGFbeta binding proteins in bovine ovaries of offspring following high or low protein diets during pregnancy of dams. Mol Cell Endocrinol 307: 133–141. doi: 10.1016/j.mce.2009.03.002
[23]
Untergasser A, Nijveen H, Rao X, Bisseling T, Geurts R, et al. (2007) Primer3Plus, an enhanced web interface to Primer3. Nucleic Acids Res 35: W71–74. doi: 10.1093/nar/gkm306
[24]
Chu T, Dufort I, Sirard MA (2012) Effect of ovarian stimulation on oocyte gene expression in cattle. Theriogenology 77: 1928–1938. doi: 10.1016/j.theriogenology.2012.01.015
[25]
Mourot M, Dufort I, Gravel C, Algriany O, Dieleman S, et al. (2006) The influence of follicle size, FSH-enriched maturation medium, and early cleavage on bovine oocyte maternal mRNA levels. Mol Reprod Dev 73: 1367–1379. doi: 10.1002/mrd.20585
[26]
Ishimi Y (1997) A DNA helicase activity is associated with an MCM4, -6, and -7 protein complex. J Biol Chem 272: 24508–24513. doi: 10.1074/jbc.272.39.24508
[27]
Li B, Castano AP, Hudson TE, Nowlin BT, Lin SL, et al. (2010) The melanoma-associated transmembrane glycoprotein Gpnmb controls trafficking of cellular debris for degradation and is essential for tissue repair. FASEB J 24: 4767–4781. doi: 10.1096/fj.10-154757
[28]
Wu R, Van der Hoek KH, Ryan NK, Norman RJ, Robker RL (2004) Macrophage contributions to ovarian function. Hum Reprod Update 10: 119–133.
[29]
Turner EC, Hughes J, Wilson H, Clay M, Mylonas KJ, et al. (2011) Conditional ablation of macrophages disrupts ovarian vasculature. Reproduction 141: 821–831. doi: 10.1530/rep-10-0327
[30]
Yu BP (1994) Cellular defenses against damage from reactive oxygen species. Physiol Rev 74: 139–162.
[31]
Mattera L, Courilleau C, Legube G, Ueda T, Fukunaga R, et al. (2010) The E1A-associated p400 protein modulates cell fate decisions by the regulation of ROS homeostasis. PLoS Genet 6: e1000983. doi: 10.1371/journal.pgen.1000983
[32]
Patel SS, Beshay VE, Escobar JC, Carr BR (2010) 17alpha-Hydroxylase (CYP17) expression and subsequent androstenedione production in the human ovary. Reprod Sci 17: 978–986. doi: 10.1177/1933719110379055
[33]
Sivko GS, DeWille JW (2004) /Enhancer binding protein delta (c/EBPdelta) regulation and expression in human mammary epithelial cells: I. “Loss of function” alterations in the c/EBPdelta growth inhibitory pathway in breast cancer cell lines. J Cell Biochem 93: 830–843. doi: 10.1002/jcb.20223
[34]
Sharma SC, Richards JS (2000) Regulation of AP1 (Jun/Fos) factor expression and activation in ovarian granulosa cells. Relation of JunD and Fra2 to terminal differentiation. J Biol Chem 275: 33718–33728. doi: 10.1074/jbc.m003555200
[35]
Andreu-Vieyra C, Chen R, Matzuk MM (2008) Conditional deletion of the retinoblastoma (Rb) gene in ovarian granulosa cells leads to premature ovarian failure. Mol Endocrinol 22: 2141–2161. doi: 10.1210/me.2008-0033
[36]
Cross MJ, Claesson-Welsh L (2001) FGF and VEGF function in angiogenesis: signalling pathways, biological responses and therapeutic inhibition. Trends Pharmacol Sci 22: 201–207. doi: 10.1016/s0165-6147(00)01676-x
[37]
Carvajal LA, Manfredi JJ (2013) Another fork in the road–life or death decisions by the tumour suppressor p53. EMBO Rep 14: 414–421. doi: 10.1038/embor.2013.25
[38]
Evans AC, Ireland JL, Winn ME, Lonergan P, Smith GW, et al. (2004) Identification of genes involved in apoptosis and dominant follicle development during follicular waves in cattle. Biol Reprod 70: 1475–1484. doi: 10.1095/biolreprod.103.025114
[39]
Skinner MK, Schmidt M, Savenkova MI, Sadler-Riggleman I, Nilsson EE (2008) Regulation of granulosa and theca cell transcriptomes during ovarian antral follicle development. Mol Reprod Dev 75: 1457–1472. doi: 10.1002/mrd.20883
[40]
Mihm M, Baker PJ, Fleming LM, Monteiro AM, O'Shaughnessy PJ (2008) Differentiation of the bovine dominant follicle from the cohort upregulates mRNA expression for new tissue development genes. Reproduction 135: 253–265. doi: 10.1530/rep-06-0193
[41]
Knight PG, Glister C (2006) TGF-beta superfamily members and ovarian follicle development. Reproduction 132: 191–206. doi: 10.1530/rep.1.01074
[42]
Matsuda F, Inoue N, Manabe N, Ohkura S (2012) Follicular growth and atresia in mammalian ovaries: regulation by survival and death of granulosa cells. J Reprod Dev 58: 44–50. doi: 10.1262/jrd.2011-012
[43]
IPA Network Generation Algorithm, White paper. Ingenuity Systems