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A transcriptomal analysis of bovine oviductal epithelial cells collected during the follicular phase versus the luteal phase of the estrous cycle.
Cerny, K L; Garrett, E; Walton, A J; Anderson, L H; Bridges, P J.
Afiliação
  • Cerny KL; Department of Animal and Food Sciences, University of Kentucky, Lexington, 40546, KY, USA. katcerny82@uky.edu.
  • Garrett E; Department of Animal and Food Sciences, University of Kentucky, Lexington, 40546, KY, USA. elise.garrett@uky.edu.
  • Walton AJ; Department of Animal and Food Sciences, University of Kentucky, Lexington, 40546, KY, USA. aisha.jamal@uky.edu.
  • Anderson LH; Department of Animal and Food Sciences, University of Kentucky, Lexington, 40546, KY, USA. les.anderson@uky.edu.
  • Bridges PJ; Department of Animal and Food Sciences, University of Kentucky, Lexington, 40546, KY, USA. phillip.bridges@uky.edu.
Reprod Biol Endocrinol ; 13: 84, 2015 Aug 05.
Article em En | MEDLINE | ID: mdl-26242217
BACKGROUND: Reproductive success depends on a functional oviduct for gamete storage, maturation, fertilization, and early embryonic development. The ovarian-derived steroids estrogen and progesterone are key regulators of oviductal function. The objective of this study was to investigate luteal and follicular phase-specific oviductal epithelial cell function by using microarray-based transcriptional profiling, to increase our understanding of mRNAs regulating epithelial cell processes, and to identify novel genes and biochemical pathways that may be found to affect fertility in the future. METHODS: Six normally cycling Angus heifers were assigned to either luteal phase (LP, n = 3) or follicular phase (FP, n = 3) treatment groups. Heifers in the LP group were killed between day 11 and 12 after estrus. Heifers in the FP group were treated with 25 mg PGF2α (Lutalyse, Pfizer, NY) at 8 pm on day 6 after estrus and killed 36 h later. Transcriptional profiling by microarray and confirmation of selected mRNAs by real-time RT-PCR analyses was performed using total RNA from epithelial cells isolated from sections of the ampulla and isthmus collected from LP and FP treatment groups. Differentially expressed genes were subjected to gene ontology classification and bioinformatic pathway analyses. RESULTS: Statistical one-way ANOVA using Benjamini-hochberg multiple testing correction for false discovery rate (FDR) and pairwise comparison of epithelial cells in the ampulla of FP versus LP groups revealed 972 and 597 transcripts up- and down-regulated, respectively (P < 0.05). Within epithelial cells of the isthmus in FP versus LP groups, 946 and 817 transcripts were up- and down-regulated, respectively (P < 0.05). Up-regulated genes from both ampulla and isthmus were found to be largely involved in cholesterol biosynthesis and cell cycle pathways, while down-regulated genes were found in numerous inflammatory response pathways. CONCLUSIONS: Microarray-based transcriptional profiling revealed phase of the cycle-dependent changes in the expression of mRNA within the epithelium of the oviducts' ampulla and isthmus.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oviductos / Células Epiteliais / Transcriptoma / Fase Folicular / Fase Luteal Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oviductos / Células Epiteliais / Transcriptoma / Fase Folicular / Fase Luteal Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article