Abstract

BackgroundDCN (decorin) is a proteoglycan known to be involved in regulating cell proliferation, collagen fibril organization and migration. In our global transcriptome RNA-sequencing approach to systematically identify new ovulation-associated genes, DCN was identified as one of the highly regulated genes. We therefore hypothesize that DCN may have a role in ovulatory processes such as cell migration and proliferation.AimTo characterize the expression, regulation and function of the proteoglycan DCN in the human ovarian follicles during the preovulatory period.MethodsThe in-vivo expression of DCN mRNA in mural (MGCs) and cumulus (CGCs) granulosa cells was characterized using quantitative RT-PCR and western blot.A signaling study was performed by treating human MGCs cultures with gonadotropins and different stimulators and inhibitors to determine their effect on DCN expression by qRT- PCR and elucidate the pathways regulating these proteins.In a functional study, KGN granulosa cell line was used to study cell migration with a scratch assay.ResultsDCN mRNA expression was significantly higher in MGCs compared to CGCs. DCN mRNA was significantly higher in CGCs surrounding mature metaphase II (MII) oocytes compared to CGCs of germinal vesicle (GV) and metaphase I (MI) oocytes.hCG significantly increased DCN mRNA and protein expression levels in cultured MGCs. Using signal transduction activators and inhibitors, we demonstrated that DCN induction by LH/hCG is carried out via PKA, PKC, ERK/MEK, and PI3K pathways.We showed that DCN expression is also induced in high-density cell cultures, in a dose-dependent pattern. In addition, progesterone induced a significant increase in DCN secretion to the media. MGCs from follicles of endometriosis patients exhibited reduced (about 20% of) mRNA transcriptions levels compared to MGCs follicles of control patients. More significantly, we found that DCN has an inhibiting effect on KGN cell migration.ConclusionsOur study indicates that DCN is a unique ovulatory gene.Our findings support the hypothesis that DCN plays an important new role during the preovulatory period and ovulation, and stress its involvement in endometriosis infertility. A better understanding of DCN role in ovulation and endometriosis may provide treatment for some types of infertility.

Highlights

  • Ovarian follicular development and ovulation in humans are highly complex and tightly regulated events [1,2,3]

  • DCN mRNA was significantly higher in CGCs surrounding mature metaphase II (MII) oocytes compared to CGCs of germinal vesicle (GV) and metaphase I (MI) oocytes. human chorionic gonadotrophin (hCG) significantly increased DCN mRNA and protein expression levels in cultured MGCs

  • Using signal transduction activators and inhibitors, we demonstrated that DCN induction by LH/hCG is carried out via protein kinase A (PKA), protein kinase C (PKC), extracellular signal-regulated kinase (ERK)/MEK, and phosphoinositide 3-kinase (PI3K) pathways

Read more

Summary

Introduction

Ovarian follicular development and ovulation in humans are highly complex and tightly regulated events [1,2,3]. The proteoglycan DCN was among the most upregulated genes in our ovulatory gene library. DCN is a member of the small leucine-rich proteoglycan (SLRP) family. It is synthesized mainly by fibroblasts, stressed vascular endothelial cells and smooth muscle cells. DCN (decorin) is a proteoglycan known to be involved in regulating cell proliferation, collagen fibril organization and migration. In our global transcriptome RNA-sequencing approach to systematically identify new ovulation-associated genes, DCN was identified as one of the highly regulated genes. We hypothesize that DCN may have a role in ovulatory processes such as cell migration and proliferation

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call