Abstract

BackgroundThe physiological state of the dominant follicle is important as it may be linked to the competence of the oocyte within. The objective of this study was to analyze, by transcriptomic analysis, the changes occurring in granulosa cells from dominant follicles at different phases of follicular growth.MethodsGranulosa cells were collected from slaughterhouse dairy cattle follicles with a diameter greater than 9 mm, and were classified at different phases of follicle growth based on flow cytometry profiles of DNA content after staining with propidium iodide. Three phases were identified based on the proportion of cells in -G1 (less than 2n DNA), G0-G1 (2n DNA) or S-M (more than 2n DNA) and follicles were thus allocated to the growing, plateau or atresia group. Between group analysis (BGA) showed clear segregation of the three groups, and the groups were contrasted against each other in a loop design to identify differently expressed genes. Ingenuity Pathway Analysis (IPA) was used to identify the functions and upstream regulators associated with the observed differently expressed genes.ResultsMajor differences were observed between the growth phases. Granulosa cells from follicles in the plateau phase had increased expression of TYRO3 and downregulation of JAM2 compared to growing follicles, supporting the idea of a shift from proliferation to differentiation. On the other hand, genes regulating the response to oxidative stress (VNN1) and angiogenesis (ANGPT2) were upregulated in granulosa cells from atretic follicles. While the predicted activated functions in cells at the plateau stage compared to cells at the growing stage included synthesis and transport of molecules, the predictions for atretic follicles relative to plateau ones included an increase in apoptosis and cell death.ConclusionConsistent with previous studies, these observations allowed us to match the presence of specific gene transcripts to a particular physiological status and consequently to classify follicles. The results also demonstrated that the plateau phase is not a simple ‘in between’ status between growth and atresia, as several characteristics are unique to this stage.Electronic supplementary materialThe online version of this article (doi:10.1186/s12958-015-0010-7) contains supplementary material, which is available to authorized users.

Highlights

  • The physiological state of the dominant follicle is important as it may be linked to the competence of the oocyte within

  • Microarray The data discussed in this publication have been deposited in NCBI’s Gene Expression Omnibus [33] and are accessible through GEO Series accession numbers GSE63904, GSE63918 and GSE63919

  • A sharp decrease in aromatase was observed in subordinate follicles when compared to dominant ones [36], and aromatase activity in dominant atretic follicles do not decrease as fast as the concentration of estradiol in follicular fluid [37,38]. These results suggest that dominant follicles may not behave in the same way as subordinate ones, and that aromatase activity may not change rapidly enough to give significant differences that would better reflect the changes observed in estradiol concentrations

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Summary

Introduction

The physiological state of the dominant follicle is important as it may be linked to the competence of the oocyte within. The objective of this study was to analyze, by transcriptomic analysis, the changes occurring in granulosa cells from dominant follicles at different phases of follicular growth. Assisted reproductive technologies (ART) are an important part of reproduction management in humans and domestic animal species, as both have to cope with fertility problems. Our understanding of the underlying causes of infertility is growing but many questions remain unanswered. As the ovarian follicle has a significant impact on oocyte quality [2] and the success of pregnancy, extensive research on follicular development is needed. We know some of the reasons why growth continues or stops, several key elements of the process remain unknown

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