The Receptive Endometrial Transcriptomic Signature Indicates an Earlier Shift from Proliferation to Metabolism at Early Diestrus in the Cow

• Autor(a) principal: Mesquita, F. S.
• Data de Publicação: 2015
• Outros Autores: Ramos, R. S., Pugliesi, G., Andrade, S. C. S., Van Hoeck, V., Langbeen, A., Oliveira, M. L., Gonella-Diaza, A. M., Gasparin, G., Fukumasu, H., Pulz, L. H., Membrive, C. M. [UNESP], Coutinho, L. L., Binelli, M.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNESP
• Texto Completo: http://dx.doi.org/10.1095/biolreprod.115.129031; http://hdl.handle.net/11449/164692
• topic: endometrium; fertility; genomics; gonadal steroids; ruminants (cows, sheep, llama, camel)

This study aimed to characterize the endometrial transcriptome and functional pathways overrepresented in the endometrium of cows treated to ovulate larger (>= 13 mm) versus smaller (<= 12 mm) follicles. Nelore cows were presynchronized prior to receiving cloprostenol (large follicle [LF] group) or not (small follicle [SF] group), along with a progesterone (P4) device on Day (D) - 10. Devices were withdrawn and cloprostenol administered 42-60 h (LF) or 30-36 h (SF) before GnRH agonist treatment (D0). Tissues were collected on D4 (experiment [Exp.] 1; n = 24) or D7 (Exp. 2; n = 60). Endometrial transcriptome was obtained by RNA-Seq, whereas proliferation and apoptosis were assessed by immunohistochemistry. Overall, LF cows developed larger follicles and corpora lutea, and produced greater amounts of estradiol (D - 1, Exp. 1, SF: 0.7 +/- 0.2; LF: 2.4 +/- 0.2 pg/ml; D - 1, Exp. 2, SF: 0.5 +/- 0.1; LF: 2.3 +/- 0.6 pg/ml) and P4 (D4, Exp. 1, SF: 0.8 +/- 0.1; LF: 1.4 +/- 0.2 ng/ml; D7, Exp. 2, SF: 2.5 +/- 0.4; LF: 3.7 +/- 0.4 ng/ml). Functional enrichment indicated that biosynthetic and metabolic processes were enriched in LF endometrium, whereas SF endometrium transcriptome was biased toward cell proliferation. Data also suggested reorganization of the extracellular matrix toward a proliferation-permissive phenotype in SF endometrium. LF endometrium showed an earlier onset of proliferative activity, whereas SF endometrium expressed a delayed increase in glandular epithelium proliferation. In conclusion, the periovulatory endocrine milieu regulates bovine endometrial transcriptome and seems to determine the transition from a proliferation-permissive to a biosynthetic and metabolically active endometrial phenotype, which may be associated with the preparation of an optimally receptive uterine environment.