Retinoid receptor-specific agonists regulate bovine in vitro early embryonic development, differentiation and expression of genes related to cell cycle arrest and apoptosis

Theriogenology

Volumn 68, Issue 8, 2007, Pages 1118-1127

  Rodriguez A ^a   Diez C ^a   Caamano J N ^a   de Frutos, C ^a   Royo, L J ^a   Munoz M ^a   Ikeda, S ^b   Facal, N ^a   Alvarez Viejo M ^c   Gomez E ^a  

^a Servicio Regional de Investigación y Desarrollo Agroalimentario de Asturias   (Spain)

^b KYOTO UNIVERSITY   (Japan)

^c HOSPITAL UNIVERSITARIO CENTRAL DE ASTURIAS   (Spain)

Author keywords

Bovine embryo; Cell cycle; Differentiation; Gene expression; Retinoids

Indexed keywords

6 [1 (5,6,7,8 TETRAHYDRO 3,5,5,8,8 PENTAMETHYL 2 NAPHTHYL)CYCLOPROPYL]NICOTINIC ACID; HISTONE; KERATOLYTIC AGENT; NICOTINIC ACID DERIVATIVE; PRIMER DNA; PROTEIN BAX; RETINOIC ACID; RETINOID X RECEPTOR; TETRALIN DERIVATIVE;

ANIMAL; ANIMAL DISEASE; APOPTOSIS; ARTICLE; CATTLE; CELL COUNT; CELL CYCLE; CHEMISTRY; DRUG EFFECT; DRUG POTENTIATION; EMBRYO (ANATOMY); EMBRYO DEVELOPMENT; FEMALE; GENE EXPRESSION REGULATION; GENETICS; PHYSIOLOGY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TIME; TUMOR SUPPRESSOR GENE;

ANIMALS; APOPTOSIS; BCL-2-ASSOCIATED X PROTEIN; CATTLE; CELL COUNT; CELL CYCLE; DNA PRIMERS; EMBRYO, MAMMALIAN; EMBRYONIC DEVELOPMENT; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENES, P53; HISTONES; KERATOLYTIC AGENTS; NICOTINIC ACIDS; RETINOID X RECEPTORS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; TETRAHYDRONAPHTHALENES; TIME FACTORS; TRETINOIN;

BOVINAE;

EID: 34848821902     PISSN: 0093691X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.theriogenology.2007.08.007     Document Type: Article

References (47)

1. Griffith M., and Zile M.H. Retinoic acid, midkine and defects of secondary neurulation. Teratology 62 (2000) 123-133
2. Roberts C., Ivins S.M., James C.T., and Scambler P.J. Retinoic acid downregulates Tbx1 expression in vivo and in vitro. Dev Dyn 232 (2005) 928-938
3. McCaffery P.M., and Dräger U.C. Regulation of retinoic acid in the embryonic nervous system: a master differentiation factor. Cytokine Growth Factor Rev 11 (2000) 233-249
4. Chambon P. A decade of molecular biology of retinoic acid receptors. FASEB J 10 (1996) 940-954
5. Mohan M., Malayer J.R., Geisert R.D., and Morgan G.L. Expression of retinol-binding protein messenger RNA and retinoic acid receptors in preattachment bovine embryos. Mol Reprod Dev 60 (2001) 289-296
6. Mohan M., Malayer J.R., Geisert R.D., and Morgan G.L. Expression patterns of retinoid X receptors, retinaldehyde dehydrogenase, and peroxisome proliferator activated receptor gamma in bovine preattachment embryos. Biol Reprod 66 (2002) 692-700
7. Mamo S., Ponsuksili S., Wimmers K., Gilles M., and Schellander K. Expression of retinoid X receptor transcripts and their significance for developmental competence in in vitro-produced pre-implantation-stage bovine embryos. Reprod Domest Anim 40 (2005) 177-183
8. Mohan M., Thirumalapura N.R., and Malayer J. Bovine cumulus-granulosa cells contain biologically active retinoid receptors that can respond to retinoic acid. Reprod Biol Endocrinol 1 (2003) 104
9. Rodríguez A., Díez C., Ikeda S., Royo L.J., Caamaño J.N., Alonso-Montes C., et al. Retinoids during the in vitro transition from bovine morula to blastocysts. Hum Reprod 21 (2006) 2149-2157
10. Faast R., Thonglairoam V., Schulz T.C., Beall J., Wells J.R., Taylor H., et al. Histone variant H2A.Z is required for early mammalian development. Curr Biol 11 (2001) 1183-1187
11. Hidalgo C.O., Díez C., Duque P., Facal N., and Gómez E. Pregnancies and improved early embryonic development with bovine oocytes matured in vitro with 9-cis-retinoic acid. Reproduction 125 (2003) 409-416
12. Thouas G.A., Korfiatis N.A., French A.J., Jones G.M., and Trounson A.O. Simplified technique for differential staining of inner cell mass and trophectoderm cells of mouse and bovine blastocysts. Reprod Biomed Online 3 (2001) 25-29
13. Vandesompele J., De Preter K., Pattyn F., Poppe B., Van Roy N., De Paepe A., et al. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol 3 (2002) 34.1-34.11
14. Duque P., Díez C., Royo L., Lorenzo P.L., Carneiro G., Hidalgo C.O., et al. Enhancement of developmental capacity of meiotically inhibited bovine oocytes by retinoic acid. Hum Reprod 17 (2002) 2706-2714
15. Gómez E., Royo L.J., Duque P., Carneiro G., Hidalgo C., Goyache F., et al. 9-cis-retinoic acid during in vitro maturation improves development of the bovine oocyte and increases midkine but not IGF-I expression in cumulus-granulosa cells. Mol Reprod Dev 66 (2003) 247-255
16. Huang F.J., Shen C.C., Chang S.Y., Wu T.C., and Hsuuw Y.D. Retinoic acid decreases the viability of mouse blastocysts in vitro. Hum Reprod 18 (2003) 130-136
17. Huang F.J., Hsu Y.C., Kang H.Y., Chang S.Y., Hsuuw Y.D., and Huang K.E. Effects of retinoic acid on the inner cell mass in mouse blastocysts. Fertil Steril 83 (2005) 238-242
18. Minegishi T., Karino S., Tano M., Ibuki Y., and Miyamoto K. Regulation of midkine messenger ribonucleic acid levels in cultured rat granulosa cells. Biochem Biophys Res Commun 229 (1996) 799-805
19. Hattori M., Takesue K., Nishida N., Kato Y., and Fujihara N. Inhibitory effect of retinoic acid on the development of immature porcine granulosa cells to mature cells. J Mol Endocrinol 25 (2000) 53-61
20. Thellin O., Zorzi W., Lakaye B., De Borman B., Coumans B., Hennen G., et al. Housekeeping genes as internal standards: use and limits. J Biotechnol 75 (1999) 291-295
21. Suzuki T., Higgins P.J., and Crawford D.R. Control selection for RNA quantification. Biotechniques 29 (2000) 332-337
22. Robert C., McGraw S., Massicotte L., Pravetoni M., Gandolfi F., and Sirard M.A. Quantification of housekeeping transcript levels during the development of bovine preimplantation embryos. Biol Reprod 67 (2002) 1465-1472
23. Goossens K., Van Poucke M., Van Soom A., Vandesompele J., Van Zeveren A., and Peelman L.J. Selection of reference genes for quantitative real-time PCR in bovine preimplantation embryos. BMC Dev Biol 5 (2005) 27
24. Cosma M.P. Ordered recruitment: gene-specific mechanism of transcription activation. Mol Cell 10 (2002) 227-236
25. Raisner R.M., and Madhani H.D. Patterning chromatin: form and function for H2A.Z variant nucleosomes. Curr Opin Genet Dev 16 (2006) 119-124
26. Leach T.J., Mazzeo M., Chotkowski H.L., Madigan J.P., Wotring M.G., and Glaser R.L. Histone H2A.Z is widely but nonrandomly distributed in chromosomes of Drosophila melanogaster. J Biol Chem 275 (2000) 23267-23272
27. Jackson J.D., Falciano V.T., and Gorovsky M.A. A likely histone H2A.F/Z variant in Saccharomyces cerevisiae. Trends Biochem Sci 21 (1996) 466-467
28. Marzluff W.F., and Duronio R.J. Histone mRNA expression: multiple levels of cell cycle regulation and important developmental consequences. Curr Opin Cell Biol 14 (2002) 692-699
29. Wu S.R., and Bonner W.M. Separation of basal histone synthesis from S-phase histone synthesis in dividing cells. Cell 27 (1981) 321-330
30. Dhillon N., Oki M., Szyjka S.J., Aparicio O.M., and Kamakaka R.T. H2A.Z functions to regulate progression through the cell cycle. Mol Cell Biol 26 (2006) 489-501
31. Giono L.E., and Manfredi J.J. The p53 tumor suppressor participates in multiple cell cycle checkpoints. J Cell Physiol 209 (2006) 13-20
32. Wang S., and El-Deiry W.S. p73 or p53 directly regulates human p53 transcription to maintain cell cycle checkpoints. Cancer Res 66 (2006) 6982-6989
33. Nishida H., Suzuki T., Ookawa H., Tomaru Y., and Hayashizaki Y. Comparative analysis of expression of histone H2a genes in mouse. BMC Genomics 6 (2005) 108
34. Li A., Chandrakanthan V., Chami O., and O'Neill C. Culture of zygotes increases p53 expression in B6 mouse embryos, which reduces embryo viability. Biol Reprod 76 (2007) 362-367
35. Migliaccio E., Giorgio M., Mele S., Pelicci G., Reboldi P., Pandolfi P.P., et al. The p66shc adaptor protein controls oxidative stress response and life span in mammals. Nature 402 (1999) 309-313
36. Favetta L.A., Robert C., King W.A., and Betts D.H. Expression profiles of p53 and p66shc during oxidative stress-induced senescence in fetal bovine fibroblasts. Exp Cell Res 299 (2004) 36-48
37. Favetta L.A., Robert C., John St.E.J., Betts D.H., and King W.A. p66shc, but not p53, is involved in early arrest of in vitro produced bovine embryos. Mol Hum Reprod 10 (2004) 383-392
38. Trinei M., Berniakovich I., Pelicci P.G., and Giorgio M. Mitochondrial DNA copy number is regulated by cellular proliferation: a role for Ras and p66(Shc). Biochim Biophys Acta 1757 (2006) 624-630
39. Orsini F., Moroni M., Contursi C., Yano M., Pelicci P., Giorgio M., et al. Regulatory effects of the mitochondrial energetic status on mitochondrial p66Shc. Biol Chem 387 (2006) 1405-1410
40. Trinei M., Giorgio M., Cicalese A., Barozzi S., Ventura A., Migliaccio E., et al. A p53-p66Shc signalling pathway controls intracellular redox status, levels of oxidation-damaged DNA and oxidative stress-induced apoptosis. Oncogene 21 (2002) 3872-3878
41. Tiberi L., Faisal A., Rossi M., Di Tella L., Franceschi C., and Salvioli S. p66(Shc) gene has a pro-apoptotic role in human cell lines and it is activated by a p53-independent pathway. Biochem Biophys Res Commun 342 (2006) 503-508
42. Hayashi K., Yokozaki H., Naka K., Yasui K., Lotan R., and Tahara E. Effect of 9-cis retinoic acid on oral squamous cell carcinoma cell lines. Cancer Lett 151 (2000) 199-208
43. Rendi M.H., Suh N., Lamph W.W., Krajewski S., Reed J.C., Heyman R.A., et al. The selective estrogen receptor modulator arzoxifene and the rexinoid LG100268 cooperate to promote transforming growth factor beta-dependent apoptosis in breast cancer. Cancer Res 64 (2004) 3566-3571
44. Pinaire J.A., and Reifel-Miller A.R. Therapeutic potential of retinoid x receptor modulators for the treatment of the metabolic syndrome. PPAR Res 2007 (2007) 94156
45. Wente W, Brenner MB, Zitzer H, Gromada J, Efanov AM. Activation of liver X receptors and retinoid X receptors induces growth arrest and apoptosis in insulin secreting cells. Endocrinology, in press.
46. Altucci L., and Gronemeyer H. The promise of retinoids to fight against cancer. Nat Rev Cancer 1 (2001) 181-193
47. Lonergan P., Rizos D., Gutierrez-Adan A., Moreira P.M., Pintado B., de la Fuente J., et al. Temporal divergence in the pattern of messenger RNA expression in bovine embryos cultured from the zygote to blastocyst stage in vitro or in vivo. Biol Reprod 69 (2003) 1424-1431