| Literature DB >> 28770380 |
Angela Maria Gonella-Diaza1, Fernando Silveira Mesquita2, Kauê Ribeiro da Silva1, Júlio Cesar de Carvalho Balieiro1, Nilton Pedro Dos Santos3, Guilherme Pugliesi3, Ricardo de Francisco Strefezzi3, Mario Binelli4.
Abstract
In cattle, the oviduct plays a major role in the reproductive process; however, molecular control of oviduct receptivity to the embryo is poorly understood. A model for receptivity based on size of the pre-ovulatory follicle (POF) was used to compare oviductal morphology, cellular proliferation, and candidate transcript abundance. Growth of the POF of Nelore (Bos indicus) cows was manipulated to produce two groups: a large POF-large corpus luteum (CL) group (LF-LCL; greater receptivity) and a small POF-small CL group (SF-SCL). Samples of the ampulla and isthmus ipsilateral and contralateral to CL were collected 4 days after GnRH-induced ovulation. Tissues were either embedded in paraffin for Harris-Hematoxylin and Eosin and periodic acid-Schiff staining and KI67 immunostaining, followed by morphological analyses, or stored at -80 °C for RNA extraction, cDNA synthesis, and qPCR analyses. The effects of group (LF-LCL and SF-SCL), region (ampulla and isthmus), and side (ipsilateral and contralateral) were analyzed using three-way nested ANOVA. The ipsilateral ampulla of the LF-LCL group presented more primary mucosal folds, a greater mucosal-folding grade and luminal perimeter, and more secretory cells and proliferating cells when compared with the ampulla of the SF-SCL group and with the contralateral ampulla of both groups. There were no morphological differences in the isthmus between groups and sides. Changes in transcript abundance are suggestive of LF-LCL-stimulated secretory activity. In summary, ovulation of a larger POF generates a periovulatory endocrine milieu that modulates morphological and functional features of the bovine oviduct which may support embryo survival and development.Entities:
Keywords: Ampulla; Cellular proliferation; Isthmus; Receptivity; Secretory cells
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Year: 2017 PMID: 28770380 DOI: 10.1007/s00441-017-2666-0
Source DB: PubMed Journal: Cell Tissue Res ISSN: 0302-766X Impact factor: 5.249